Zoophysiology Volume 39

Editors:
S.D. Bradshaw W. Burggren
H.C. Heller S. Ishii H. Langer
G. Neuweiler D.J. Randall

Springer-Verlag Berlin Heidelberg GmbH

Zoophysiology
Volumes already published in the series:

Volume 1: P.J. Bentley Volume 22: WH. Dantzler

Endocrines and Osmoregulation (1971) Comparative Physiology of the Vertebrate
Kidney (1988)
Volume 2: L. Irving
Arctic Life of Birds and Mammals Volume 23: G.L. Kooyman
Including Man (1972) Diverse Divers (1989)
Volume 3: A.E. Needham Volume 24: S.S. Guraya Ovarian
The Significance of Zoochromes (1974) Follicles in Reptiles and Birds (1989)
Volume 4/5: A. C. Neville Volume 25: G.D. Pollak and ].H. Gasseday
Biology of the Arthropod Cuticle (1975) The Neural Basis of Echolocation in Bats
(1989)
Volume 6: K. Schmidt-Koenig
Migration and Homing in Animals (1975) Volume 26: G.A. Manley
Peripheral Hearing Mechanisms in Reptiles
Volume 7: E. Curio and Birds (1989)
The Ethology of Predation (1976)
Volume 27: U.M. Norberg
Volume 8: W Leuthold Vertebrate Flight (1990)
African Ungulates (1977)
Volume 28: M. Nikinmaa
Volume 9: E.B. Edney
Vertebrate Red Blood Cells (1990)
Water Balance in Land Arthropods (1977)
Volume 10: H.-U. Thiele Volume 29: B. Kramer
Carabid Beetles in Their Environments (1977) Electrocommunication in Teleost Fishes (1990)

Volume 11: M.H.A. Keenleyside Diversity and Volume 30: W Peters

Adaptation in Fish Behaviour (1979) Peritrophic Membranes (1991)

Volume 12: E. Skadhauge Volume 31: M.S. Kaulenas

Osmoregulation in Birds (1981) Insect Accessory Reproductive Structures
(1992)
Volume 13: S. Nilsson
Autonomic Nerve Function in the Vertebrates Volume 32: A.L. Val and V.M.F. de Almeida-Val
(1983) Fishes of the Amazon and their Environment
(1995)
Volume 14: A.D. Halsler
Olfactory Imprinting and Homing in Salmon Volume 33: R. Wiltschko and W Wiltschko
(1983) Magnetic Orientation in Animals (1995)
Volume 15: T. Mann Volume 34: S.B. Moffett
Spermatophores (1984) Nervous System Regeneration in the
Invertebrates (1996)
Volume 16: P. Bouverot
Adaption of Altitude-Hypoxia in Vertebrates Volume 35: H. Kobayashi and Y. Takei
(1985) The Renin-Angiotensin System (1996)
Volume 17: R.].F. Smith Volume 36: L. Aitkin
The Control of Fish Migration (1985) Hearing - the Brain and Auditory
Volume 18: E. Gwinner Communication in Marsupials (1998)
Circannual Rhythms (1986) Volume 37: f.N. Maina
Volume 19: f.C. Ruegg The Gas Exchangers: Structure, Function,
Calcium and Muscle Activation (1986) and Evolution of the Respiratory Processes
(1998)
Volume 20: f.-R. Truchot
Comparative Aspects of Extracellular Acid-Base Volume 38: G. Kuchling
Balance (1987) The Reproductive Biology of the Chelonia
(1999)
Volume 21: A. Epple and ].E. Brinn
The Comparative Physiology of the Pancreatic Volume 39 (2"d ed. of Vol. 1): P.f. Bentley
Islets (1987) Endocrines and Osmoregulation (2002)
P.J. Bentley

Endocrines and
Osmoregulation
A Comparative Account in Vertebrates

Second Edition of Volume 1

With 30 Figures and 23 Tables

~Springer
Prof. Dr. Peter J. Bentley
The University of Western Australia
Dept. of Physiology
Nedlands, Western Australia 6907

ISSN 0720-1842

The first edition was published 1971 as Volume 1 of the series.

Library of Congress Cataloging-in-Publication Data

Bentley, P.J.
Endocrines and osmoregulation : a comparative account in vertebrates I by P.J. Bentley. - 2nd ed.
p. cm.
lncludes bibliographical references and index.
ISBN 978-3-642-07657-2 ISBN 978-3-662-05014-9 (eBook)
DOI 10.1007/978-3-662-05014-9
1. Osmoregulation. 2. Endocrinology. 3. Vertebrates - Physiology. I. Title.
QP90.6 .B45 2002
573.4'16 - dc21
2001054976
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Springer-Verlag Berlin Heidelberg GmbH .
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Dedication

To Sebastian Dicker For Friendship

Preface to the Second Edition

The opportunity to prepare a second edition of a book that was originally written
over 30 years ago has provided me with both a challenge and a source of pleas-
ure; the former as it needed to be spatially constrained within its original limits.
Nevertheless, over 1000 references have been added. I must apologize to the many
biologists whose contributions could not be included. I have attempted to keep
the original format and historical perspective. The information has been princi-
pally described within the context of each phyletic group of the vertebrates and
their habitats. Each chapter is reasonably self-contained, but appreciation of mate-
rial in later chapters, as often indicated, can be amplified by reference to Chap-
ters 1 and 2. Information that was provided in tables in the first edition has now
often been summarized in the text. Reviewing the work of earlier contributions
to this field of study has evoked many pleasant memories of friends and acquain-
tances, some deceased, events and occasions. It has been a particular pleasure to
perceive the consequences of such observations and know some of the answers
to the questions that they raised. A new generation of such questions has now
emerged, which is one of the reasons for preparing this summary.
I would like to thank Professor Don Bradshaw for suggesting that this book
may be welcome and Springer-Verlag for making it possible. The Physiology
Department and the Biological Sciences Library of the University of Western
Australia have provided me with the facilities and succour that I needed to com-
plete this book. Dr. Norman Goodchild provided invaluable help in preparing
some of the figures for the publisher. Thank you all.

Peter Bentley
The University of Western Australia
December 2001
Preface to the First Edition

It is an old and trite saying that a preface is written last, placed first and read least.
It may also be an explanation or justification for what follows, especially if the
author feels that the reader may not agree with him. This is, thus, something of
an apologia.
When I first agreed to write this book, I felt that it was to be directed princi-
pally towards the endocrine system of vertebrates, especially as there were
available some excellent accounts of their osmoregulation. However, it was soon
apparent to me that in order to appreciate the role of the endocrines, one must
strongly emphasize non-endocrine functions involved in the regulation of the
animals' water and salt balance. In addition, several years have elapsed since a full
account of vertebrate osmoregulation has been given. I have thus felt free to take
an overall look at the animals' water and salt metabolism, but have especially
emphasized more recent contributions. Possibly the book should now be called
Osmoregulation and the Endocrines.
A rather conventional format has been retained for, despite many claims to
the contrary, I do not feel that all things new, experimental and innovative are
necessarily desirable. In the first two chapters I have attempted to introduce,
and summarize, at a general level, the two major topics, osmoregulation and
endocrines, while emphasizing the diversity of such processes in the vertebrates.
In the second chapter I have also included a section on the Criteria, Methods and
Difficulties of experimental comparative endocrinology. I felt that this informa-
tion may be useful for the reader who desires to make a critical appreciation and
evaluation of many of the experiments that are described. It may, hopefully, also
be useful to the younger workers interested in comparative endocrinology and
help them to glean something about the sort of work that they may expect to do.
The vertebrate groups have been described within the framework of their
customary classification, a decision arrived at primarily because this also makes
a little evolutionary sense. Some have questioned the wisdom of placing the
mammals first, and travelling down, rather than up, the phyletic scale. However,
each chapter is reasonably complete in itself so that those who disagree can resort
to the subterfuge of reading the book backwards.
I have attempted to relate the physiology of the various beasts to that of the
environments that they normally occupy. At the same time I have not hesitated
to descend to the more currently fashionable "molecular level". I hope that this
may help both to remind some of the more "mature" readers and to emphasize
to the younger ones the very broad scope of interest that animals have to offer. It
is principally for the younger group that this book has been written.

New York P.f. Bentley

1970
Acknowledgements (First Edition)

The observations of many people, only some of whom are quoted, made this book
possible. I would like to extend my thanks to all who have contributed to these
subjects and only wish that it would have been possible to acknowledge the work
of all.
The latter part of this book was written while I was a guest of the Commis-
sariat a L'Energie Atomique. I would like to thank them for their hospitality, par-
ticularly Professeur J. Coursaget, Chef du Departement de Biologie, and Dr. Jean
Maetz and his Groupe de Biologie. The help and guidance of Jean Maetz made the
latter part of this book possible. Dr. Erik Skadhauge kindly gave me some advice
on avian matters.
The Mount Sinai School of Medicine of the City University of New York kindly
granted me leave so that I could join the Commissariat a L'Energie Atomique. A
number of nice ladies have helped me during the various stages in preparation of
this manuscript; special thanks are due to Mrs. Jean Homola, Mrs. Norma Beasley,
Miss Marguerite Murphy and Mrs. Wolina Shapiro.
My wife showed considerable forbearance and gave much-needed help in
the final preparation of the proofs. The editorial help and advice of Dr. D. S.
Farner is gratefully acknowledged as well as the cooperation of the staff of
Springer-Verlag in Heidelberg and Mr. B. Grossmann in New York.
Contents

Chapter 1 Osmotic Problems of Vertebrates ...................... .

General Introduction .......................................... .
1 Geographical and Ecological Distribution of the Vertebrates
(Osmotic Distribution) ....................................... .
2 The Osmotic Anatomy of the Vertebrates. . . . . . . . . . . . . . . . . . . . . . . . . 4
3 Osmotic Exchanges with the Environment. . . . . . . . . . . . . . . . . . . . . . . . 8
3.1 Physico-Chemical Gradients with the Environment............. 8
3.2 Size and Surface Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. .
3.3 Nature of the Integument. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
3.4 Metabolism and Oxygen Consumption..... . .......... ... .... 9
3.5 Feeding................................................. 9
4 Forces Affecting Exchanges of Water and Solutes . . . . . . . . . . . . ... . . . 9
4.1 Diffusion. . . . . . . . . . . . . . . . . . . . . . . . . . . . . ............ . . .
4.2 Facilitated Diffusion. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10. . . . . . . .
4.3 Osmosis................................................. 10
4.4 Evaporation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11. . . . . ....
4.5 Active Solute Transport. . . . . . . . . . . . . . . .... . ....... 11. . .. . . ...
5 Transporter Proteins Involved in Solute and Water Movements
Across Cell Membranes............................ ..... ....... 12
6 Biological Structures Participating in Fluid Exchange . . . . . . . . . . . . .20 .
6.1 The Cell Membrane . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 . . . . . . ...
6.2 Capillaries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 . . . ... . .
6.3 Skin......... ... ..... . .. .. . . ............................ 23
6.4 Water Loss from the Tetrapod Respiratory Tract . . . . . . . . . . . . . 24. .
6.5 Gills . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 ... . .... .
6.6 Gut . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 . .. ......
6.7 Urinary Bladder.............. . ....... .... ................ 31
6.8 Salt Glands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32. . . . . . . .
6.9 Kidney . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .34. . . . . . . . .
6.9.1 Functions............. ... .. . ............. ......... . 34
6.9.2 Structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .34 . . .... ..
6.9.3 Physiology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .36 . . . . . . . . .
6.9.4 Regulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38 . .. ... . . .
7 Relationships of Nitrogen Metabolism to Osmoregulation . . . . . . . . . . 39.
8 Osmoregulation and the Evolution of Vertebrates...... . ........... 41

Chapter 2 The Vertebrate Endocrine System . . . . . . . . . . . . . . . . . . 45. . . .

1 Endocrine Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45. . . . . . . . . .
 1.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . ....... 46
. ... . . . . .
1.2 Architecture of Hormones and Receptors . . . . . . . . . . . . . . . . . 46 .. . .
1.3 Morphology of the Endocrine Glands . . . . . . . . . . . . . . . . . . .48. . . . .
1.4 Synthesis of Hormones . . . . . . . . . . . . . . . . . . . . . . . . . . .49. . . . . . . .
1.5 Release of Hormones . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50. . . . . . . .
1.6 Hormones in the Blood . . . . . . . . . . . . . . . . . . . . . . . . . . .51. . . . . . . .
1.7 Peripheral Metabolism of Hormones......................... 51
1.8 Mechanisms of Hormone Action . . . . . . . . . . . . . . . . . . . . . 52 . .. . . ..
2 Osmoregulatory Hormones................................... . 57
2.1 The Hypothalamus and Pituitary Gland........... .. ....... . . 60
2.2 The Renin-Angiotensin System (RAS)........................ 66
2.3 Adrenocorticosteroids . . . . . . . . . . . . . . . . . . . . . . . . . . . .68 . . .....
2.4 Adrenaline and Noradrenaline. .. ........................... 71
2.5 The Natriuretic Peptide Hormones . . . . . . . . . . . . . . . . . . . . . 72 . . . . .
2.6 Adrenomedullin...... ... ... .......... ..... ....... .. ...... 74
2.7 Guanylin Peptides........................................ 75
2.8 The Thyroid Hormones . . . . . . . . . . . . . . . . . . . . . . . . . . 76 . . .. . . ..
2.9 The Urotensins . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
. .. ... .
3 Mechanisms of the Hormonal Regulation of Water and Salt
Across Epithelial Membranes . . . . . . . . . . . . . . . . . . . . . . . . . .78 . . .. . .. .
3.1 Vasopressin and Vasotocin....... ... .. . ...... . ........... .. 78
3.2 Mineralocorticoid Hormones. . . . . . . . . . . . . . . . . . . . . . . 81... . . . ..

Chapter 3 The Mammals . . . . . . . . . . . . . . . . . . . . . . . . . . . . .85 . . . . . . . .

1 General Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85 . . .. . . ..
2 Osmoregulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .86 . ...... .
2.1 Water Loss . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87 . . .. ... .
2.1.1 Cutaneous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87 .. . .. ...
2.1.2 Respiratory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88 .. . . . ..
2.1.3 Renal Water Loss . . . . . . . . . .. . ........ . . . . . . 88 . . . . .. . .
2.1.4 Faecal Water Loss . . . . . . . . . . . . . . . . . . . . . . . . . . 90 . .. .. . ...
2.1.5 Water Loss Associated with Reproduction . . . . . . . . . . . . 90 ..
2.2. Salt Loss. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91 . . . .... ..
2.2.1 The Sweat Glands.. . ............. ...... ............. 91
2.2.2 The Gut . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .91 . . . . . . . .
2.2.3 The Kidney . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
.. .. ....
2.3 Accumulation of Water and Salts . . . . . . . . . . . . . . . . . . . . . .94 . . .. . .
2.4 Effects of Dehydration on the Body Fluids . . . . . . . . . . . . . . . . .96 ...
3 The Monotremes (Egg-Laying Mammals) . . . . . . . . . . . . . . . . . . . 97 .. . ..
4 The Marsupials (Pouched Mammals)... ...... . . .. .... ........... 98
5 The Placental Mammals .... ................................... 105

Chapter 4 The Birds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113 .. . ..... .

1 Water Loss..................... .... .. ...... ................. 116
1.1 Evaporative . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117
. . ... . .
1.2 Urinary and Faecal . . . . . . . . . . . . . . . . . . . . . . . . . . . . 119 . .. ... . . .
1.3 Renal Water Conservation and the Neurohypophysis . . . . . . . . . .120 .

XIV
2 Conservation and Excretion of Salts . . . . . . . . . . . . . . . . . . . . . . . .122
.....
2.1 Kidneys........ . ......................... .. ............. 123
2.2 Nasal Salt Glands . . . . . . . . .......... . . . . . . . . . . . .124 ... . . . ..
3 Conservation of Water and Salt by the Cloaca and Large Intestine.... 126
4 Sources of Water and Salts . . . . . . . . . . . . . . . . . . . . . . . . . . . . .128 . . . . . . .
4.1 Food..... . .. . .. . .. .. . . .. . ..... . ......... .. ..... . ....... 128
4.2 Drinking . . . . . . . ..... . ..... . .................. 128 . . . . . .
5 Reproduction, Migration and Osmoregulation . . . . . . . . . . . . . . . . . .130
..
6 Osmoregulation and Hormones in Free-Living Birds . . . . . . . . . . . . 132
. ..

Chapter 5 The Reptiles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .133 .. . ...

1 Water Exchanges.. . .. . ..... . ............................ .. . . . 137
1.1 Skin and Respiratory Tract. . ............... . .. . .. . ... . .. . .. 137
1.2 Urinary and Faecal Water Loss . . . . . . . . . . . . . . . . . . . . . . . . . .139.. . .
1.2.1 Role of the Kidney . . . . . . . . . . . . . . . . . . . . . . . . . .140 ..... . ..
1.2.2 Role of the Cloaca-Colon Complex. . . . . . . . . . . . . . . . 142
. ....
1.2.3 Role of the Urinary Bladder.......... . .. . ............. 143
2 Salt Exchanges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 144
...... .
2.1 Skin..... . ..... . ....... . .. . ..................... . ..... . . 144
2.2 Kidney . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .145 .. . ......
2.3 Cloaca and Urinary Bladder...... .. ..... . .. ... .... .. .. . ... . 147
2.4 Cephalic Salt Glands . . . . . . . . . . . . . . . . . . . . . . . . . . . . 148
. .........
3 Accumulation of Water and Salts . . . . . . . . . . . . . . . . . . . . . . . 151
. .. . ... ..
4 Reproduction and Osmoregulation.. . ... . ...... . ....... . ....... . 152

Chapter 6 The Amphibia . . . . . . . . . . . . . . . . . . . . . . . . . . . .155 . .........

1 Water Exchange . ........... . .. . ... . .... . . . ................... 163
1.1 Skin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .163 . . .......
1.1.1 In Water. .. . . .... .. . . .. . .......... . .. . ........... . . 163
1.1.2 In Air . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .167 . ..
1.2 The Kidney . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 168 . ..... . ..
1.3 The Urinary Bladder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .171. . ......
1.4 The Large Intestine (Colon) . . . . . . . . . . . . . . . . . . . . . . . 172
. ........
2 Salt Exchange . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .173 . . ......
2.1 Skin . . . . . . . . .. . . . .. . ....... . . . . . . . . . . . . . .174 ..............
2.2 The Kidney . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .177 .......
2.3 The Urinary Bladder . . . . . . . . . . . . . . .. . ....... . . . . 178
...... . ..
2.4 The Large Intestine (Colon) .. .. . ..... . ............... . .... . 180
3 Nitrogen Metabolism . . . . . . . . . . . . . . .. ........ . . . . . . . .181... . .. .
4 Reproduction............ . ... . . . ....................... . . ... . 182
5 Accumulation of Water and Salt . . . . . . . . . . . . . . . . . . . . . . . . . . . . 184
... .

Chapter 7 The Fishes . . . . . . . . . . . .. . . ....... . . . . . . . . . . 187 . . . . . . . .

1 The Piscine Endocrines . . . . . . . . .. ...... . . . . . . . . . . . . . .190.........
1.1 Neurohypophysial Hormones . ................... . ... . ... .. . 191
1.2 Adrenocorticosteroids.. . .. . ........... . . . ... . ............. 191
1.3 The Renin-Angiotensin System. .. . . ........................ . 192

XV
 1.4 Natriuretic Peptides . . . . . . . . . . . . . . . ........ . . . . . 193 . . ..... ..
1.5 Catecholamines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 193 . .. .. .. . .
1.6 Thyroid Hormone . . . . . . . . . . . . . . . . . . . . . . . . . . . . .194 .. ... ....
1.7 Urotensins I and II........................................ 194
1.8 The Growth Hormone/Prolactin Family . . . . . . . . . . . . . . . . . . .195
. . .
2 Water Exchanges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 197 . ...... . .
2.1 The Skin and Gills . . . . . . . . . . . . . ... . .. . . .. ..... .198 .. . . . ... .
2.2 The Gut . . . . . . . . . . . ... .. . ... . . ..... . . . . . . . 199 ..............
2.3 The Kidney . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .202 . . . .... . .
3 Salt Exchanges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .206 . . ... ...
3.1 The Skin and Gills . . . . . . . . . . . . . . . . . . . . . . . . . . . . .207 .. .... . ..
3.2 The Kidney........................... . .................. 217
3.3 The Urinary Bladder...................................... 218
3.4 The Gut.. . .. . ........................................... 219
4 Nitrogen Metabolism and Osmoregulation . . . . . . . . . . . . . . . . . . . 220 . . . .
5 Osmoregulation and the Endocrines of Sharks and Rays . . . . . . . . . .221 .
6 The Hagfish . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .228 . . .... .. .

References . . . . . . . . . . . .. . .. . . ... . . . .... . . . . . . . . 233

. . . . .......

Index . . . . . . . . . . ... . ........ . . . . . . . . . . . . . . . . . 285

.... .. .. .

XVI
Chapter 1

Osmotic Problems of Vertebrates

General Introduction
Water provides the vehicle and molecular framework in which life on earth is
maintained and perpetuated. It is the host and mentor of the macromolecules of
proteins and nucleic acids that are intrinsic to this process. Under prevailing
cosmic conditions water exhibits many chemical and physical properties that
contribute to the stability, tertiary structure and replication of such proteins and
nucleic acids, and the normal functioning of the assembled organism. Molecules
of water in liquid form are electrically dipolar and readily form hydrogen bonds
with each other and neighbouring compounds. They can also dissociate to
provide essential hydrogen and hydroxyl ions. The physical properties of water
include an appropriate diffusible and bulk mobility, tensile strength and a rela-
tively high heat capacity, boiling point, melting point and heat of vaporization.
Water acts as a solvent for crystalline salts such as sodium and potassium chlo-
rides, which can then form electrically charged ions (Na+, K+, en. Such ions can
participate in processes involving the transmission of information and the trans-
formation of energy. Many other molecules, including essential nutrients and
carbon dioxide, can dissolve in water. The properties and behaviour of water may
be changed by the presence of such solutes, which can disturb hydrogen bonding,
change the solubility and tertiary structures of macromolecules and decrease its
mobility. The marriage of water and solutes is essential for the perpetuation of
life, but can sometimes lead to disharmony. Osmoregulation is the process that
attempts to forestall and correct such problems.
The vertebrates originated about 500 million years ago, probably evolving from
a marine protochordate. They have since dispersed to occupy many diverse habi-
tats. This colonization of the planet is exemplified by the great variety of extant
species. A synoptic classification of such vertebrates is provided in Table 1.1. It is
principally based on their anatomy and physiology and reflects, and illustrates,
their progressive evolution. It is intended to provide a useful framework for the
subsequent discussion of their osmoregulation.

1 Geographical and Ecological Distribution of the Vertebrates

(Osmotic Distribution)
While it is uncertain if the vertebrates originated in the sea or fresh water, sub-
sequently both environments, as well as the dry land, have been occupied by rep-
Table 1.1. A classification of the vertebrates

Phylum Chordata
Subphylum Urochordata (tunicates)
Subphylum Cephalochordata (amphioxus)
Subphylum Vertebrata
Superclass Agnatha (jawless fishes, cyclostomes)
Class Myxini
Order Myxiniformes (hagfish)
Order Pteraspidomorpha (includes extinct ostracoderms)
Class Cephalaspidopmorpha
Order Osteostraci (extinct ostradoderms)
Order Petromyzontiformes (lampreys)
Superclass Gnathostomata (jawed vertebrates)
Class Placodermi (extinct heavily armoured jawed fish)
Class Chondrichthyes (cartilaginous fish, placoid scales, no swim bladder)
Subclass Elasmobranchii (uncovered gill slits)
Order Selachimorpha (Squaliformes) (sharks)
Order Batoidimorpha (Rajiformes) (skates, rays)
Subclass Holocephali (gill slits covered, chimaeras, ratfish, rabbitfish)
Class Osteichthyes (bony fish, gill slits covered, bony scales, usually a swim bladder)
Subclass Actinopterygii (ray-finned fishes, includes most extant bony fishes)
Superorder Chondrostei (partly cartilaginous skeleton, mostly extinct)
Order Acipenseriformes (sturgeons, paddlefish)
Order Polypteriformes (African freshwater bichirs and reedfish, also classified In the
Subclass Brachyioptergii)
Infraclass Holostei
Order Lepisosteiformes (freshwater gars)
Order Amiiformes (freshwater bowfin)
Infraclass Teleostei (most extant bony fishes)
(The Holostei and Teleostei are also classified as being in the Superorder Neopterygii)
Subclass Sarcopterygii (Choanichthyes) (lobe-finned fishes)
Superorder Crossopterygii (most extinct)
Division Rhipidistia (extinct, possible ancestors of the amphibians)
Division Coelacanthiformes (one extant marine species, Latimeria chalumae, the
coelacanth)
Superorder Dipnoi (lungfish, three extant freshwater genera)
Tetrapoda (an informal name for vertebrates with four legs: amphibians, reptiles, birds and
mammals)
Class Amphibia (phyleticaly highest anamniotes, mostly terrestrial, aquatic larvae, soft
permeable skin)
Subclass Lissamphibia (includes all extant amphibians)
Order Apoda (Gymnophiona) (caecilians; limbless, tropical and subtropical, burrowing
or aquatic)
Order Urodela (Caudata) (tailed amphibians, newts and salamanders)
Order Anura (Salientia) (frogs and toads)
Amniotes; an informal grouping of reptiles, birds and mammals, extraembryonic membranes
form a developmental sac enabling eggs to be laid on dry land.
Class Reptilia (formerly predominant land vertebrates, ectodermal scales, metanephric
kidney)
Subclass Anapsida
Order Chelonia (Testudinata) turtles, terrapins, tortoises
Subclass Lepidosauria (a diapsid skull)
Order Rhynchocephalia (Sphenodonta) (lizard-like reptiles from the Triassic, one extant,
Spenodon punctatus)
Order Squamata (include majority of extant reptiles)
Suborder Ophidia (Serpentes) (snakes)

2
Table 1.1. Continued

Suborder Lacertilia (Sauria) (lizards)

Subclass Archosauria ("ruling reptiles", include the dinosaurs and bird stock)
Order Crocodilia (crocodile, alligators, caimans, gavials)
Class Aves (birds, feathered vertebrates)
Subclass Neornithes
Superorder Palaeognathae (ratite running flightless birds, ostriches, emus, rheas. No keel
on sternum)
Superorder Neognathae (carinate birds, with a keel on the sternum, which usually fly.
About 20 extant orders, the Passeriformes (perching birds) comprise about half of all
bird species.)
Class Mammalia (vertebrates with hair and which suckle their young)
Suclass Prototheria (egg-laying mammals)
Infraclass Monotremata (monotremes, echidna, platypus)
Subclass Theria
Infraclass Metatheria (yolk sac forms placenta, relatively undeveloped at birth)
Order Marsupialia (marsupials, young usually suuckled in an pouch)
Cohort Ameridelphia (N. and S. American marsupials, includes opossum)
Cohort Australidelphia (Mostly live in Australia and New Guinea, one order In
S. America. Kangaroos, wallabies, possums, koala, wombats etc.)
Infraclass Eutheria (placentals, a "true" allantoic placenta)

resentatives of most of the major groups. The geographicallocation(s) for the

transition to a vertebrate is also unknown, but subsequent dispersal has been
widespread. The major groups of fishes, the Agnatha, Chondrichthyes and Oste-
ichthyes, have representatives in the sea and fresh water. The tetrapods are pri-
marily terrestrial, but the Amphibia, reptiles, birds and mammals, all have species
that normally live in marine or freshwater environments. Osmoregulatory
processes play a major role in such dispersal, and it is not surprising to observe
that the physiological mechanisms by which such adaptations take place, often
differ greatly. Even among the fishes, an apparently novel occupation of a certain
medium may represent a secondary, tertiary or even further removed alteration
of the habitat that was primary in the group. Darlington (1957) has traced the
probable historic origins of the endemic catfishes of Australia: teleost fish origi-
nated in the sea from whence a fish related to the order Isospondyli moved into
fresh water to give rise to the order Ostariophysi. Some of this group probably re-
entered the sea and returned subsequently to fresh water in Australia. Among the
tetrapods at least one amphibian, the crab-eating frog, Rana cancrivora, has
returned to a marine environment, and even more numerous examples of such a
transition can be seen among the reptiles, that have marine and freshwater as well
as terrestrial representatives. The biological adaptations accompanying such tran-
sitions are sometimes very similar in different groups, providing examples of con-
vergent evolution. In other instances, more novel and unique mechanisms have
evolved. Thus, both the marine frog, Rana cancrivora, and the sharks and rays
maintain their body fluids hyperosmotic to sea-water by accumulating urea. On
the other hand, marine reptiles like the loggerhead turtle, Caretta caretta, have
body fluids similar in concentration to their terrestrial relatives which is hypos-
motic to sea-water. However, they can excrete salt as a highly concentrated solu-

3
tion from a modified orbital gland. Thus, Rana cancrivora has evolved a mecha-
nism parallel to that of the sharks and rays, while the reptiles have utilized a novel
mechanism not seen in their phyletic forbears. Both similarities and diversities
in osmoregulatory mechanisms are found within, and between, the major phyletic
groups of vertebrates.
The vertebrates have occupied most of the earth's geographic areas, being
sparse in the cold terrestrial polar regions, and not as numerous in hot dry deserts
as in the wetter tropical zones. The desert regions, where the supply of water may
be limiting to life, make up about one third (50 million square kilometers) of
the land surface of the earth (Schmidt-Nielsen 1964a). Despite the potential osmo-
regulatory problems, vertebrates do live in even the extremely dry parts of such
desert areas, and exhibit interesting physiological and behavioural patterns
consistent with their life there. The seas have a diverse vertebrate fauna of fish,
reptiles, birds and mammals. Major geographic limitations exist for the various
vertebrate groups and will be discussed later, but in the instance of the Amphibia
and reptiles, they are dictated mainly by temperature rather than by water.
Geographic dispersal, followed by genetic isolation, has played an important
role in the process of evolution. Both the ability and inability to osmoregulate
in different situations have played a part in breaking and maintaining the physi-
cal barriers involved. Deserts can retard the dispersal of animals (Darlington
1957), as shown by the distribution of the Amphibia in Australia. Darwin (1839)
considered the sea to be the major physical barrier to dispersal, a view that
is still current (Darlington 1957). The sea constitutes the most effective barrier
to the movement of the freshwater fishes, and Darwin noted the absence of
Amphibia and terrestrial mammals from most oceanic islands, where reptiles
are frequent inhabitants. This probably reflects the osmoregulatory powers of the
different groups. Reptiles, with their less permeable integument, considerable
tolerance to internal osmotic change, extrarenal salt excretion and marked
independence of environmental temperature, would appear to be better suited
to prolonged oceanic voyages than freshwater and terrestrial Amphibia and
mammals. At Duke University I kept a freshwater turtle, Pseudemys scripta, for 30
days in sea-water. At the end of this time it was sluggish and had a plasma sodium
concentration of nearly 300 mEq l-', but on being returned to fresh water it
resumed its normal life. Prolonged oceanic voyages are thus conceivable, even by
contempory species of freshwater-terrestrial reptiles, a tribute to their osmoreg-
ulatory capabilities.

2 The Osmotic Anatomy of the Vertebrates

Water is the predominant constituent of living organisms. In vertebrates it nor-

mally makes up about 70% of the total body weight and there are no consistent
differences between the phyletic groups. However, tolerance to dehydration can
vary. Humans can only tolerate a loss of water equivalent to about 12% of their
body weight (Adolph 1947) and this value appears to be similar to that in other
mammals. Some frogs, such as the Australian desert species Cyclorana platy-

4
 cephala can survive, following rehydration, a loss by evaporation of 50% of their
body weight (Main and Bentley 1964). However, tree frogs (Litoria, formerly
Hyla), also from Australia, die after losing half this amount of water. Mortality
due to water loss appears to reflect several events, including the effects of the
increased osmotic and solute concentrations on tissue life processes and a failure
of the blood circulatory system. The total body water is sequestered in separate
regions (spaces or compartments) that have different chemical compositions.
Their size can be estimated by measuring the volume of distribution of chemical
markers such as inulin and Evans blue in the body fluids. Fluid equivalent to about
45 to 55% of a vertebrate's body weight is present inside cells (intracellular com-
partment) where it is contained by the cell membranes. The extracellular fluid
(the inulin space) amounts to 15 to 25% of the total body weight (it varies from
about 16% in some fish to 25% in other vertebrates) and is divided into the blood
plasma (measured with Evans blue) and the intercellular (or interstitial) fluids.
The two latter fluid compartments are separated by the capillaries. The plasma
contains higher concentrations of proteins than the intercellular fluid. The
plasma volume may be as low as 2% of the body weight in some fish but it is
usually about 5%. The physiological maintenance of these different fluid com-
partments primarily depends on the functioning of the cell membranes and the
cardiovascular-capillary systems. Secondarily, it depends on the regulation of the
solute levels in the extracellular fluid. This process results from the activities of
the kidneys and gut, and phyletically diverse salt-secreting tissues such as salt
glands in some fish, reptiles and birds, and the gills in many fish.
The osmotic concentrations in the different fluid compartments in the body
are similar, though their particular solute constituents differ. The composition of
the extracellular and intracellular fluids differs; the latter has relatively high con-
centrations of K+ while in the former the Na+ and Cl-are higher (Tables 1.2, 1.3).
(In humans the total body content of osmotically active K+ is 46mmolkg- 1 body
weight while that of Na+ is 42mmolkg- 1: Thorn 1960.) The intracellular concen-
trations of K+ and Na+ are remarkably similar in different vertebrates (Table 1.3 ).
Such uniformity appears to reflect requirements for the stability and activity
of their contained macromolecules, especially those of enzymes (see Yancey
et al. 1982). However, the total intracellular osmotic concentrations of solutes can
vary in different species. In some marine fish, such as hagfish (Agnatha), sharks
and rays (Chondrichthyes) and the coelacanth, Latimeria (Crossoptergygii), it is
similar to that of the sea-water in which they live. Nevertheless, the concentra-
tions of salts in the intracellular fluids of such fish remain similar to those in
other vertebrates (Table 1.3). The differences between the ionic and total osmotic
concentrations are mainly made up by the presence of organic solutes (osmolytes)
such as amino acids, urea and methylamine compounds including trimethy-
lamine oxide (TMAO) and betaine. The extracellular fluids are not as fastidious
with respect to their salt content, as the intracellular fluid and the salt concentra-
tion may be increased to achieve an osmotic balance in some species, especially
hagfish (Table 1.2). In sharks and rays and the coelacanth, organic osmolytes,
including urea, may also be accumulated in the extracellular fluids. Such organic
osmolytes appear to have minimal perturbing effects on the activity of cell macro-
molecules as compared to increased levels of inorganic ions. However, in many

5
Table 1.2. Principal osmotic constituents of the blood plasma or serum of various species

Osmotic cone. Na K Cl Urea

(mosmolkg-1 H 20) (mmolkg-1 H20 or 1- 1)

Sea-water about 1000 470 10 550

Fresh water 0.2-25 0.1-6 0.06-0.11 0.03-13
Invertebrates
Cuttlefish• SW 465 22 591
Vertebrates
Agnatha
Hagfishh SW 969 487 9 510
(Myxine glutinosa)
Lamprey FW 270 120 3 96 <1
(Lampetra fluviatilis)
Chondrichthyes
Spiny dogfish' SW 980 296 7 276 308
(Squalus acanthias) TMAO 72
Freshwater sawfish FW 540 170 130
(Pristis microdon)
Amazon stingrayrl FW 308 146 135 <1
(Potamotrygon sp.)
Osteichthyes
Coelacanth' SW 957 105 53 100 290
(Latimeria chalumnae) TMAO 109
African lungfish FW 238 99 8 44 500
(Protopterus aethiopicus)
(aestivation)
Flounder SW 364 194 5 166
FW 304 157 5 114
(Platichthys flesus)
Amphibia
European green toad 279 113 5 99 16
(Bufo viridis)
Aestivation 3 monthsr 1320 231 181 900
Crab-eating frogg (80% SW) 830 252 14 227 350
(Rana cancrivora)
Reptilia
Bobtaillizardh Winter 151 5
(Tiliqua rugosa)
Summer 196 5
Birds
Gull1 154 4
(Larus glaucescens)
Mammals
Laboratory rat 324 150 6 119 7

The remainder of the information is from the summary of Bentley (1971a).

FW = fresh water; SW = sea-water.
a Robertson (1965).
h Robertson (1976).
' Robertson (1975).
d Gerst and Thorson (1977).
' Lutz and Robertson (1971).
r Degani et al. (1984).
8 Gordon et al. (1961).
h Bentley (1959).
1 Holmes et al. (1961).

6
Table 1.3. Intracellular solute concentrations in various species

Na K Cl Amino Urea TMAO Betaine

mmolkg- 1 acids
water

Sea-water 470 10 550

Bacteria
Salmonella (150mM NaCl) 131 238 <5 109
Halobacterium 400-800 7500 3610 209
salinarium (5.1 M NaCl)
Invertebrate
Cuttlefish (Sepia 31 189 483 86 108
officianalis) SW
Vertebrates
Hagfish (Myxine 32 142 41 291 2 87
glutinosa) SW
Spiny dogfish (Squalus 18 130 13 333 180 100
acanthias) SW
Coelacanth (Latimeria 30 74 35 290 442
chalumnae) SW
Flounder (Platichthys 10 157 30 44 14
jlesus) SW
FW 15 158 42 71 30
Green toad (Bufo viridis) 30 95 17 100 17
Laboratory rat 16 152 5 3 7

Based on Yancey eta!. (1982) and Bentley {1971a). Bacteria from Christian and Waltho (1962).

instances some osmolytes may also exert protective "counteracting" effects with
respect to possible adverse actions of high concentrations of urea. Thus, TMAO
can counteract the protein-perturbing effects of urea when the ratio urea/TMAO
is about 2. Other such counteracting osmolyes are glycerophosphocholine and
betaine. Compatible osmolytes, where the presence of such counteracting solutes
is not needed, include polyols, such as sorbitol and glycerol, simple amino acids
and amino acid derivatives such as taurine. An accumulation of organic
osmolytes, especially urea, has also been observed to occur in several amphibians
including the crab-eating frog, Rana cancrivora, which lives among coastal man-
groves in Southeast Asia. Some toads that live in desert conditions may experi-
ence prolonged periods of seasonal drought when water is not freely available.
They may then live in burrows, such as seen in the European green toad, Bufo
viridis. Some amphibians may also aestivate under such conditions and form pro-
tective cocoons, as observed in the Australian water-holding frog Cyclorana platy-
cephala. Under such conditions these toads can store high concentrations of urea
in their body fluids (Table 1.2). African lungfish, Protopterus aethiopicus, aestivate
in mud chambers when their water habitat dries up and they also store urea in
their body fluids until water again becomes available.
In 1962, Christian and Waltho described the intracellular ion concentrations
in a remarkable archaea bacterium, Halobacterium salinarum, which lives in
concentrated solutions of brine (Table 1.3). Potassium concentrations of over
4570mmolkg- 1 water were observed. In mammals this concentration is about
150 mmol kg- 1 water. The enzymes present in these bacteria appear to have under-

7
gone considerable adaptation that involves many intramolecular amino acid sub-
stitutions. Such adaptations reflect another way of adjusting to life in solutions of
high osmotic concentration that does not require a continual extra expenditure
of energy for active osmoregulation or the synthesis of organic osmolytes.
However, the strategic use of organic osmolytes may be a simpler evolutionary
solution to such osmotic problems and reflect parsimonious "genetic simplicity"
(Yancey et al. 1982}.

3 Osmotic Exchanges with the Environment

Water, solutes and nutrients continually move in and out of animals in a pattern
that results ideally in their "steady state" with the environment. Man of the
osmotic exchanges are obligatory for the animal and not under its direct control,
though their magnitude determines the extent of the regulatory processes that
are ultimately necessary in order to achieve the steady state.
This obligatory osmotic exchange or turnover depends on several aspects of
the animal's physiology.

3.1 Physico-Chemical Gradients with the Environment

Differences between the chemical composition of an animal and its environment

will influence water and solute movements in, or out of, the beast. Thus, aquatic
species in fresh water will tend to accumulate water and lose solutes, while the
opposite usually occurs in fishes living in the sea. Temperature gradients will
influence evaporative water losses especially for cooling in homoiotherms.

3.2 Size and Surface Area

Exchange of water and solutes is related to surface area. Large animals have a
relatively smaller surface area exposed to the environment than small animals.
The gill surface in fishes varies considerably and, apart from a relation to the
animal's size, may reflect the normal oxygen needs of the species.

3.3 Nature of the Integument

The barriers exposed to the environment vary in their permeability to water and
solutes. Thus, the skin of the Amphibia is usually more permeable to water than
that of reptiles, while the gills of elasmobranch fish are less permeable to solutes
than those of the teleosts.

8
3.4 Metabolism and Oxygen Consumption

The exchanges of oxygen and carbon dioxide in terrestrial animals are usually
accompanied by water loss, due to saturation of the expired air with water vapour.
Metabolism is accompanied by the production of heat and waste solutes; the first
facilitates evaporative water loss, while the latter often requires body water for its
excretion.

3.5 Feeding

Excess water and solutes may be taken in with nutrients. Animals consuming a
succulent herbivorous diet containing 98% water will usually have a water intake
in excess of their needs, while a diet of marine invertebrates will provide super-
fluous salt.
The magnitude of these effects varies considerably in different species. Water
exchanges in a day may be equivalent to as much as 50% of the body water in the
leopard frog, Ran a pipiens, or less than 1% in a lizard like the chuckwalla, Sauro-
malus obesus. The daily sodium exchange of a marine fish, like the flounder, is
more than 20 times as great as the total sodium content of the body, but in man
this exchange represents only about 3% of the total present.

4 Forces Affecting Exchanges of Water and Solutes

The osmotic composition of vertebrates differs considerably from that of their

external environments. As described above, there are also considerable differences
between the solute concentrations in the body fluid compartments within the
animal itself. The external environment tends to dissipate such concentration gra-
dients. Animals exploit a variety of strategies to counter such forces and main-
tain their chemical composition at levels that are consistent with life. The primary
barriers across which such physico-chemical forces act are cell membranes. They
exhibit a selective permeability to the solutes and water that tend to travel across
them. In some instances they may even incorporate biological mechanisms that
can reverse such dissipative molecular flows.

4.1 Diffusion

Molecules in solutions, both solutes and solvent, tend to move from regions of
their higher to their lower concentration. This process of diffusion occurs as a
result of random molecular movements dictated by their thermal energy. Equili-
bration with adjoining phases may be restricted by the presence of the mem-
branes with which the molecules may collide. The number of molecules eventually

9
crossing such a barrier in unit time is called the flux and will depend on the prop-
erties of the membrane (the permeability coefficient), the concentration of the
molecule and, if it is an ion with an electrical charge, the electrical potential dif-
ference (PD) that may exist between the two sides of the membrane. Such dif-
fusible movements of molecules will simultaneously occur between the phases on
each side of the membrane (influx and efflux). The rate will be greatest down the
steepest electrochemical gradient and result in a net flux. Ultimately, without
further biological intervention an equilibrium state will be established when no
further net change will occur.

4.2 Facilitated Diffusion

Molecular equilibration across biological membranes may sometimes occur more

rapidly than predicted. Such facilitation can reflect an interaction with a mem-
brane-associated carrier that speeds its transmembrane diffusion. A variety of
such carriers have been identified (see later). It should be emphasized that no
direct input of additional energy is involved in this type of diffusion. The carrier-
molecule complex moves through the membrane by diffusion but more rapidly
than the molecule would alone.

4.3 Osmosis
When two solutions with different solute concentrations are separated by a
semipermeable membrane (that limits or excludes movement of the solute) there
will be a net movement of solvent, by diffusion, from the side with the lower to
that with the higher solute concentration. This movement of solvent is called
osmosis and commonly influences the movements of water both within the
body and between the animal and the aqueous environment that it occupies.
The application of an opposing hydrostatic pressure will impede the movement
of the solvent. If the solution on one side is pure solvent then the pressure that
must be applied to stop net water transfer is called its osmotic pressure. At 0 °C,
a pressure of 2.26 megapascals (Mpa) is required to prevent movement of
water across a semipermeable membrane into a 1-osmolal solution. (Osmotic
effects are proportional to the number of molecules in solution so that a molal
solution of a salt, such as sodium chloride, which ionizes into more than one
constituent, will exert a proportionally higher osmotic pressure than, for inst-
ance, a molal solution of urea.) Solutions with identical osmotic concentrations
are described as being iso-osmotic or isosmotic to each other, while solutions
with different concentrations may be hyperosmotic or hypo-osmotic (hypos-
motic) to each other. These are physico-chemical terms. Isotonic, hypertonic and
hypotonic are the equivalent biological terms and refer to such solutions with
reference to their potential abilities to influence the volumes of living cells
and organisms.

10
4.4 Evaporation
The transformation of a liquid (or solid) into a vapour or gas is called vaporiza-
tion or evaporation. Kinetically, it can be viewed as an escape of molecules with
a greater than average kinetic energy from a liquid to a gas phase. The excess
kinetic energy of the departing molecules of water will be lost from the liquid
and a loss of heat will result. At a physiological temperature of about 35 oc this
heat loss will be about 584 calories g- 1 (2443 Joules). Heat lost as a result of evap-
oration from the skin and respiratory tract plays a vital role in thermoregulation
in mammals and birds. Evaporation is also the major cause of dehydration in ter-
restrial vertebrates. The particular structure of the skin and its functioning as a
barrier membrane are important determinants of the rate of evaporation that
occurs in terrestrial vertebrates.
Evaporation of water occurs more rapidly at higher environmental and skin
temperatures, at low barometric pressures, and when the vapour pressure of water
in the gas phase is low. Evaporation will cease when the latter is saturated with
water vapour (the saturated vapour pressure) and this value increases with
increased temperature. The thickness of the adhering layer of water vapour at the
interface between the skin and the gas phase is particularly important as it con-
tributes to the length of the pathway across which the water must diffuse. If mix-
ing with the surrounding air is slow, evaporation will decrease, as the diffusion
pathway will be impeded. Thus, increased wind speed and convectional air move-
ments will facilitate evaporation by decreasing the effective thickness of this
boundary layer. The structure and arrangement of scales, hair and feathers
can retard or promote evaporation by influencing the mixing of this layer with
the external air. Secretion from skin glands can provide water for evaporation.
The blood supply to the skin will affect the temperature at this external interface.
Evaporation from the body surface can thus be influenced by a variety of factors.
For practical comparisons of rates of evaporative water loss of different
animals the values can be corrected for skin surface area and expressed in terms
of the vapour pressure difference or saturation deficit. This value is the difference,
in mmHg, between the saturated water vapour pressure of the air over a free water
surface at the ambient environmental temperature and the actual vapour pres-
sure of the water that is present. However, this adjustment provides only an
approximation of comparative rates of evaporation. Measurements of evapora-
tion from the skin can be used to calculate the animals skin resistance (r; units
are as scm- 1) to water loss (Spotila and Berman 1976; Robertson and Smith 1982).
Values for r can be used for interspecific comparisons of evaporation between
animals. It allows for differences due to the thickness of the external boundary
layer of air such as may result from the mixing effects of different rates of air flow.

4.5 Active Solute Transport

Active transport of molecules has been defined by Hans Ussing ( 1960) as "a trans-
fer which cannot be accounted for by physical forces". Solute movements down

11
the sum of gradients of chemical concentration, electrical potential, temperature,
pressure and as a result of drag (frictional) forces accompanying solvent move-
ment do not constitute active transport. Transport against the sum of such gra-
dients across biological membranes requires the expenditure of energy (usually
supplied by ATP) by the cell into or out of which the solute transfer is occurring.
Currently, active transport is often classified as primary active transport and sec-
ondary active transport. The former refers to a process in which there is a direct
utilization of energy by the molecular mechanism that promotes the solute trans-
fer. For instance, the active extrusion of Na+ from cells as a result of its interac-
tion with Na-K-activated ATPase (Na-K-ATPase, the Na pump). On the other
hand, chloride ions (en can also be transported actively against prevailing elec-
trochemical gradients into cells. However, this process does not involve a direct
linkage of the cl- to an energy-consuming event. Two cl- are instead coupled to
the transfer of K+ and Na+ on a carrier molecule that can diffuse across cell mem-
branes. This carrier utilizes the diffusion gradient of Na+ concentration created
by Na-K-ATPase to cross the cell membrane. This process, which is called cotrans-
port, is an example of secondary active transport (see Table 1.4). In effect, it uti-
lizes a tandem-like linkage of solutes and the processes of both facilitated
diffusion and active solute transport.
The possibility of an active transport of water has received sporadic and some-
times semantic attention, but it is generally not considered to be a widespread
process. However, "molecular water pumps" are currently receiving some atten-
tion (MacAulay et al. 2001). The forces of osmosis, diffusion and hydrostatic
pressure appear to account for most movements of water across biological mem-
branes. There remain some phenomena, such as the movement of water across
the mammalian intestine, that defy such an explanation and could involve sec-
ondary active transport.

5 Transporter Proteins Involved in Solute and Water Movements

Across Cell Membranes
Careful experimental measurements involving the processes of solute and water
movements across cell membranes resulted in the prediction of the presence of
various "pumps", "carriers", and "pores" or"channels" in cells. The enzyme Na-K-
ATPase, or Na pump, was originally identified and purified using classical bio-
chemical procedures. Recombinant DNA techniques have since been utilized for
the identification and cloning of a host of genes that express proteins that func-
tion as such pumps, channels, exchangers and cotransporters when expressed in
cells (expression cloning) such as the oocytes of the toad Xenopus laevis. Thus,
molecular entities involved in basic osmoregulatory processes, which were once
considered to be hypothetical concepts, are now available for direct study. To the
amazement of some, they have actually been shown to exist! Some of these trans-
port proteins are summarized in Table 1.4.

12
Table 1.4. Some molecular transport proteins (pumps, carriers and channels) associated with
epithelial membranes that participate in osmoregulation

Transport protein Action Principal sites

Ion pumps (primary active transport)

Na•-K•-ATPase (P-type)' 3Na• out of cells and 2K+ in All cells, basolateral side
in epithelia
H•-K•-ATPase (P-type, colonic K+ absorption and H+ Apical surface late distal
isoform)b secretion renal tubule and colon
Proton (W)-ATPase (V-type)' H+ secretion, secondary Apical surface late distal
absorption HCO,-, Na• renal tubule, frog skin,
fish gills, turtle bladder

Ion channels (uniporters, diffusion pathways)

Epithelial Na• channels (ENaC)d Na+ absorption Apical surface late distal
nephron, colon, frog skin
and bladder etc.

Inward rectifying K+ channels' (K1, gene family)

ROMK Maintain negative membrane Apical surface distal
PD, K+ secretion nephron, thick ascending
loop of Henle
Recycling K+ across Basolateral side kidney,
basal plasma membrane intestine and (?) gills

Ct channelsr
CIC family (voltage-gated) Transepithelial Ct, cell Kidney, intestine, muscle
volume regulation
CFTR (cAMP-sensitive) (Cystic Ct and fluid secretion Apical and basal side;
fibrosis conductance regulator) intestine, bronchi, salt
glands, (?)gills etc.
Volume-sensitive organic anion Cell volume regulation Ubiquitous
channels (VSOAC)S

Ion exchangers (antiporters, secondary active transport)

Na+/H+ (NHE gene family)h Acid-base balance, Na• Most cells, apical side
absorption, regulation renal tubule, intestine,
cell volume gills
Acid base balance, Ct Many cells; apical, basal
absorption, regulation side, gills, intestine, frog
cell volume skin
Limits accumulation Na• Muscle, gills

Ion cotransport (symporters, secondary active transport)

Na+-K+-zCJ-k (NKCC) Cell volume regulation, Many cells, thick
cl- absorption, secretion, ascending loop of Henle,
K+ secretion intestine, salt glands, gills
Absorption Na+, Ct Distal convoluted renal
tubule, fish bladder,
intestine

13
Table 1.4. Continued

Transport protein Action Principal sites

Cell volume regulation, Many cells; renal tubule,

extrusion K+ and Cl- intestine
Acid-base regulation, Proximal and thick
HCo,- absorption ascending limb renal
tubule, intestine
2Na+-glucose" (SGLT)-amino Nutrient, Na+ absorption Kidney tubule, intestine
acid
Na+-, Na+-Cl-osmolyteso Cell volume regulation Kidney cells

Urea transporters
UT-AP Maintain renal medullary Renal collecting ducts
concentration gradients
Urea conservation Elasmobranch kidney,
gills(?)
Na+-linked urea cotransporterq·' Urea conservation Elasmobranch kidney,
gills(?), mammal kidney
Aquaporins' (water channels) Cell volume regulation Cell membrane, may be
enhance osmotic flows and unilateral
conservation of water
AQP1 Renal tubule; proximal,
thin loop Henle
AQP2 Responsive to vasopressin Renal cortical collecting
duct, amphibian bladder
AQP3 Renal medullary
collecting duct, intestine
AQP4 Renal medullary
collecting duct
AQP8 Colon

' Robinson (1995), Blanco and Mercer (1998).

b Wingo and Smolka (1995), Silver and Soleimani (1999), Jaisser and Beggaln (1999).
' Ehrenfeld et al. (1985), Harvey (1992a,b), Lin and Randall (1995).
d Canessa (1996), Garty and Palmer (1997), Horisberger (1998).
• Jan and Jan (1994), Lee and Hebert (1995), Schultz (1997), Giebisch (1998), Derst and Karschin
(1998).
f Larsen (1991), Silva et al. (1999a), Jentsch et al. (1999), Sheppard and Welsh (1999), Evans
et al. (1999).
8 Perlman and Goldstein (1999).
h Wakabayashi et al. (1997), Perry (1997).
' Kopito and Lodish (1985); Larsen (1991); Perry (1997).
; Ussing (1947), Motais et al. (1966).
k Xu et al. (1994), Mount et al. (1998), Isenring et al. (1998), Russell (2000).
1 Mount et al. (1998).

m Romero and Boron (1999).

" Crane (1965); Hediger et al. (1987).

o Burg (1995), Perlman and Goldstein (1999).
P Sands et al. ( 1997).
q Smith and Wright (1999).

' Part et al. (1998).

' Yamamoto and Sasaki (1998); Heyman and Engel (1999), Borgnia et al. (1999).

14
 Ion Pumps. A variety of macromolecules can actively transport solutes, in-
cluding ions, across cell membranes utilizing processes that depend energetically
on the hydrolysis of ATP. Such pumps (Table 1.4) make basic contributions to the
regulation of ion concentrations and the fluid volume of cells and the composi-
tion of the extracellular fluid. Na-K-ATPase and H-K-ATPase belong to a super-
family of such macromolecules that have been identified in a variety of organisms
including bacteria, fungi, plants and animals. Comparisons of their structures
indicate that they have evolved from a distant, but common, ancestor. They are
called the P-type ATPases (Prefers to the common mechanism of their phospho-
rylation). Na-K-ATPase is the prototype that was first identified in crab nerves.
It appears to be present in all animal cells, where it mediates the active extru-
sion of Na+ from the cytosol and the accumulation of K+ from the extracellular
fluid. This pump can thus regulate the cell's volume and maintain the inwardly
directed gradient of Na+ concentration that is necessary for the movements by
diffusion of various Na+-linked cotransporters (see below) across the cell mem-
brane. Thus, Na-K-ATPase has a vital basic physiological role in maintaining the
osmoregulatory activities of cells. It spans the cell membrane in which it may have
a quite uniform symmetrical distribution or, as seen in epithelial cells, be con-
fined to their basolateral borders. This enzyme is heteromeric and consists of
two or three subunits; a (about 112kDa), ~ (40 to 60kDa) andy (8 tol4kDa).
The precise structures are homologous, but vary in different species. Isomers are
often present in a single animal and may each contribute to the special needs of
particular cells. Specific binding sites for Na+, K+, ATP and inhibitory molecules,
such as the drug ouabain, are present. The cycle of their functioning involves
allosteric changes in molecular structure between E-1 and E-2 forms. Initially,
three Na+ combine from the cytosolic side with sites on the a-subunit, and this
interaction results in hydrolysis of the ATP, phosphorylation of this subunit and
its transformation to the E-2 form. The three Na+ then dissociate from the mole-
cule at the extracellular face of the cell. Two K+, from the extracellular fluid, then
combine with the a-subunit and, along with the phosphate, subsequently disso-
ciate from its cytosolic side. The E-1 configuration is then restored. The ~-subunit
is necessary for the normal activity of the process of activity of the enzyme but
its precise function is unknown. The role of the y-subunit, which is sometimes
present, is also obscure. Regulation of the activity of Na-K-ATPase may involve
responses to ion concentration, and the actions of mediators, which in vertebrates
include adrenocortical steroid hormones and catecholamines (Therien and
Blostein 2000). Regulation involves quantitative increases of the enzyme as a
result of genetic expression, changes in its distribution, its affinity for solutes and
its rate of degradation. The H-K-ATPase exists in several isomeric forms and has
been identified in the apical plasma membrane of epithelial cells in the
mammalian colon and renal tubule. It contributes to the secretion of H+ and
absorption of K+.
A variety of H+-ATPases are present in nature, but one type appears to have
special roles in ion regulation. It was first identified in the vacuolar membranes
of plants and belongs to a distinct genetic group called the V-type ATPases.
This enzyme is present in the apical plasma membrane of a variety of ion-
transporting epithelial cells including frog skin, turtle urinary bladder, fish gills

15
and distal regions of the mammalian renal tubule. It secretes three H+ per ATP
molecule, which results in the generation of an electrical potential difference
across the cell membrane. Apart from promoting the conservation of HC0 3- by
the kidney (H+ + HC0 3- ~ H2C0 3 ~ C0 2 + H2 0) it creates a favourable electri-
cal gradient to promote the entry of Na+ into epithelial cells. This Na+ may then
be actively extruded across the opposite basolateral surface due to the action of
Na-K-ATPase.

Ion Channels (Uniporters ). The cell membrane contains a diversity of proteins,

often oligomeric, that incorporate channels that have selected abilities to allow
the diffusion of solutes, including Na+, K+ and Cl-, from one side of the membrane
to the other. Such flows of ions are usually unidirectional, or subject to substan-
tial rectification. Such properties reflect the molecular makeup of the channels
which influence the dimensions, electrical charges, the presence of specific
binding sites and the activities of restricting gates. Such gates can open and close
in response to such stimuli as changes in membrane voltage, mechanical stretch
due to cell volume changes, the local concentrations of ATP and Ca2+, and the
activities of phosphorylation mechanisms mediated by G-proteins and cAMP (see
Chap. 2). The opening and closing of ion channels can also be promoted by
neurotransmitters and hormones. The different ion channels are expressed by
specific genes, and several forms may exist for each type of ion. Such variations
appear to reflect their different roles and the activities of the tissues in which they
are present. As summarized in Table 1.4, apart from contributing to the electrical
activities of cells sodium channels, potassium channels and chloride channels are
frequently involved in the osmoregulatory activities of epithelial cells such as are
present in the kidney tubules, gut, salt glands and gills. Ion channels are present
in all organisms. Similarities in the structures of ion channels from distantly
related organisms suggest the possibility that they may have an "evolutionary
kinship" {Jan and Jan 1994; Derst and Karschin 1998).

Ion Cotransporters (Symporters ). The entry or exit of Na+, K+ and cl- from cells
can be facilitated by a variety of specific carrier protein molecules that are present
in the cell membrane. Mutually dependent linkages of ions and solutes such as
Na+-cl-, K+ -cl-, Na+-K+ -2Cl- and Na+ -glucose activate various cotransporter
carrier proteins, which then diffuse across the cell membrane. The driving force
for such diffusion into the cell is the low concentration of Na+ inside the cell, or,
in the case of the exit of K+-cl-, that of K+ in the extracellular fluid. Such gradi-
ents are primarily maintained as a result of the activity of Na-K-ATPase. These
processes and their cotransport carrier proteins are widespread in nature and
have been identified in vertebrates, invertebrates and plants (Mount et al. 1998).
They play important roles in the regulation of cell volume and the processes of
secretion and absorption of ions, especially cl-, in epithelia such as the kidney
tubules, gut, various salt glands and fish gills. The first description of such a linked
mechanism involved the cotransport of Na+ and glucose across the intestine
(Crane 1965). This process also occurs in the renal tubule, where in the proximal
segment it accounts for about 50% of the Na+ absorption. The first demonstration
oflinked Na+-K+-2Cl- transport was made by Geck and his collaborators ( 1980)

16
in cultured Ehrlich tumour cells. The genes for several such carriers have been
cloned, including Na+-cl- (originally from the urinary bladder of flounder,
Gamba et al. 1993) and Na+-K+-zcl- (from the shark rectal gland, Xu et al.
1994). Homologous proteins have since been identified at many other sites in
humans and other species. Comparisons of the structures of Na+-cl-, Na+-K+-
2Cl- and K+-cl- cotransporter proteins indicate that they belong to a common
gene family which share structural motifs with such proteins in invertebrates and
plants.
The transport of HC0 3- across epithelial tissues such as the proximal renal
tubule and gut can occur in association with Na+ and involves a cotransport
protein that has been dubbed NBC {Table 1.4). Bicarbonate transport can also
takes place in a process that involves the activity of a CI-/HC0 3- exchange protein.
The NBC and Cl-/HC03- membrane proteins have a 30 to 35% identity in their
amino acid sequences and thus appear to belong to a common bicarbonate ion
transporter family. The stoichiometry of Na+ and HC0 3- transport in NBC varies
from 1 : 1, which is electrically neutral, to 1 : 3, which is electrogenic.

Ion Exchangers (Antiporters). There are a number of ion transport mecha-

nisms in cell membranes which utilize electrically neutral exchanges of two
cations or two anions. Such exchanges can be homogeneous, such as Na+/Na+, or
heterogeneous, such as Ct/HC03- and Na+/H+ (Table 1.4). One of the ions moves
down its electrochemical gradient while the other may move against it. There
is no direct input of new energy into such processes, which are described as
countertransport.
An early example of the involvement of such processes in the osmoregulatory
activities of epithelia was discovered by A. Krogh in 1937. He demonstrated a
cl-/HC03- and Na+/NH/ exchange that could account for the active uptake of
NaCl across the skin of frogs maintained in solutions with a low salt concentra-
tion. Respiratory physiologists have long been aware of the process of cl-/HC03-
exchange which occurs across the erythrocyte cell membrane when it unloads
accumulations ofHC03- for subsequent excretion as carbon dioxide. This process,
called the chloride shift, assures that the process is electrically neutral and that
no change in cell volume occurs. It involves the interaction of CI- and HC03- with
a specific cell membrane protein called the band 3 protein. Structural relatives of
this anion exchange protein have been identified from other tissue sites and have
been cloned (Alper et al. 1988). They occur in the kidney tubules, gut and the gills
of fish, where they contribute to the regulation of pH, cell volume and trans-
epithelial Cl- transport.
Several Na+/H+ion exchange transport proteins have been cloned from human
tissues (NHE proteins) (Sardet et al. 1989). Their presence in cells is ubiquitous,
where they contribute to the regulation of pH and cell volume {NHE1). Others,
for instance NHE3, are present in the apical plasma membranes of epithelial cells
in kidney tubules, gut and fish gills, where they are involved in the uptake and
transepithelial transport of Na+. The activities of these proteins appear to be
directly regulated by cell pH but they also can respond to external stimuli such
as growth factors and hormones that may act by a process involving their
phosphorylation.

17
 Urea Transporters. Urea, as described earlier, can function as an osmolyte in
cells and extracellular fluids especially in elasmobranch fish that live in the sea.
It also has an important role in maintaining local hyperosmotic gradients in the
medullary tissue of the kidneys of mammals. At this site it subserves their ability
to form a hyperosmotic urine. Urea has a high solubility in water but a low one
in lipids, yet it readily crosses lipoidal cell membranes. Such anomalous behav-
iour suggested that it may utilize special pathways for entry into cells. Physiolog-
ical observations on its urinary excretion suggest that in some species special
mechanisms, including active transport, may exist in the renal tubule which
fosters its conservation. Vasopressin, the antidiuretic hormone that promotes
osmotic absorption of water from the distal regions of the renal tubule, has also
been observed to increase the permeability of epithelia to urea, as observed in
frog skin and toad urinary bladder in vitro. This response is also seen in the renal
tubules of mammals, amphibians and elasmobranch fish (Sands et al. 1997; Smith
and Wright 1999). These effects of vasopressin on urea are specifically blocked by
the drug phlorizin. There is thus a considerable amount of evidence suggesting
the presence of specific urea carriers in cell membranes. The use of gene cloning
and expression techniques has resulted in the identification of several urea trans-
porter proteins (Table 1.4). They are present in a variety of tissues including ery-
throcytes, brain and kidney, and include the products, UT-A and UT-B, of at least
two genes in mammals. An isoform of UT-A (UT-A2) from the rabbit kidney was
the first to be cloned (You et al.1993). It is a glycoprotein (about 43kDa). UT-A1,
cloned from rat kidney, can be activated by vasopressin to transport urea. The
reaction appears to involve its phosphorylation as a result of the action of protein
kinase A. A urea transporter has also been cloned from the kidney of the dogfish
shark, Squalus acanthias. It has been called shUT and is structurally similar to
UT-A2, suggesting that they may belong to a common protein family. These urea
transporters facilitate the diffusion of urea down concentration gradients across
cell membranes.
Proteins that possibly mediate an active transport of urea have not yet been
directly identified. However, as described earlier, experimental observations
suggest that they may exist in the kidneys of mammals, amphibians and elasmo-
branchs. They could be mediating a Na+-linked secondary active transport of urea
(an Na+-urea cotransporter). Such a linkage has been observed during the activ-
ity of the Na+-glucose cotransporter (Leung et al. 2000).

Aquaporins. The lipoidal nature of the cell membrane is expected to consider-

ably restrict the transport of water between the cell and its bathing solutions.
Nevertheless, substantial movements of water do occur, which appear, at least
partly, to involve diffusion between the interstices of hydrocarbon chains in the
lipids. However, in many cells, such as erythrocytes, water moves much more
rapidly than expected and exhibits low activation energy, about 5 kcal mol- 1, which
is similar to that of the diffusion of water in water. The water thus appears to be
moving through an aqueous phase across cell membranes, suggesting that water-
filled protein channels or pores may be present. Such a rapid transfer of water
may be necessary for adequate adjustments of cell volume, the secretion of fluids

18
and the massive reabsorption of water that takes place across the epithelia of the
renal tubules and gut.
The frog and toad urinary bladder (in vitro) provide models for studying the
transepithelial water permeability of the distal regions of the renal tubule and its
response to vasopressin. (Vasopressin is the hormone that decreases urinary
water excretion in mammals.) In 1974 Chevalier et al., using a freeze-fracture
etching technique, were able to visualize, by electron microscopy, "membrane-
associated particles" in the apical cell membrane of frog bladder epithelial cells.
The presence of these MAPs, was found to be associated with increases in osmotic
water transfer, which occurred in response to the action of a vasopressin-like
hormone (oxytocin). The particles were thought be proteins and provided a bio-
logical reality to formerly hypothetical water channels.
In 1984, a protein was identified in the cell membranes of ocular lens fibre cells
Gorin et al. 1984). As it makes up about 60o/o of the total protein present at this
site it was called major integral protein or MIP. At the time of its identification its
function was unknown, but it is now thought to contribute to the loss of water by
the lens fibre cells. Its absence in mice results in lens opacity (cataracts) and blind-
ness. In 1992 the aqueous water channel in erythrocyte cell membranes was
cloned by Agre and his collaborators (Preston et al. 1992). When expressed in
oocytes of the toad Xenopus, it was found to behave as a water channel, which
was subsequently called aquaporin 1. MIP (now called aquaporin 0) was found to
be a similar protein that belongs to a large family (aquaporin or MIP family) of
proteins. These molecules contain water channels or, in some, glycerol channels.
About 160 such related proteins have been identified in species that include bac-
teria, archaea, plants and animals. So far, ten such aquaporins have been identi-
fied in mammals. They are homotetramers, with each monomer (about 30kDa)
containing a membrane-spanning water-filled pore which excludes ions but may
have a limited permeability to molecules such as glycerol. The tissue sites and
functions of some of these proteins are shown in Table 1.4. Aquaporin 2 is present
in the renal collecting duct (Fushimi et al.l993) and can be inserted into the apical
cell membrane in response to the presence of vasopressin. It appears to be syn-
onymous with the MAPs observed in 1974 by Bourguet and his collaborators
(Chevalier et al. 1974) in the frog urinary bladder.
Other molecular mechanisms exist which may facilitate the movements of
water across cell membranes, but their quantitative contributions to water trans-
fer do not appear to be as great as those of the aquaporins. However, they may
have special roles. Several molecular transporter proteins that are primarily
involved in solute transport have been shown to also mediate water transport.
Their effects are not directly related to osmotic changes induced as a result of
possible changes in cell solute concentrations. They have been called molecular
water pumps. The most closely studied are the K+-Cl-, and the 2Na+-coupled
glucose (SGLTl) (Table 1.4) and the Na+-coupled glutamate cotransporters
(EAATl). Allosteric changes associated with the activation of such transporter
proteins possibly induce the opening of water channels which are a part of the
molecule or closely associated with its functioning (Fischbarg et al. 1990; Zeuthen
1991; Loo et al.1999a; MacAulay et al. 2001). The SGLTl protein couples the trans-

19
port of 2Na+, 1 glucose and 200-260 water molecules. The activation energy for
the water transport is about 5kcalmol-1, which is similar to that observed for
aquaporins. The physiological and quantitative contributions of such molecular
water pumps to the large movements of water that occur across the kidney tubules
and intestine is contentious (Loo et al. 1999b; Spring 1999). Clearly, a major part
of the fluid movement across the epithelial membranes is linked to Na+transport,
but the precise mechanism is uncertain. In the intestine, Spring tentatively favours
the ingenious Curran three-compartment model (Curran 1965). This theory
involves a coupling of primary active Na+ transport with secondarily generated
osmotic and hydrostatic forces in three neighbouring compartments in the tissue.
As a result of the generation of these forces, water movement is predicted to occur
from the lumen of the gut to the blood side. The morphological presence and
functioning of all these compartments remains to be demonstrated to the satis-
faction of all. The precise physiological roles of molecular water pumps is also
uncertain.

6 Biological Structures Participating in Fluid Exchange

The fluids of the body are separated from each other by the cell membrane and
capillary, and from the external environment by the skin, by the epithelia of the
respiratory organs (gills and lungs) and the gut. The integrity of the intracellular
fluid is dependent on the cell itself and its surrounding membrane, as well as the
composition of its bathing (extracellular) fluids. The regulation of the compo-
nents of the extracellular fluid is due principally to the activities of kidneys, but
also to the functioning gills, various "salt" glands, the gut and even the skin in
some species.

6.1 The Cell Membrane

The outer physical barrier of the cell is called the cell membrane or plasma mem-
brane. It separates the inner cytoplasm from the extracellular fluid, and restricts,
monitors and regulates the molecular exchanges which occur between these two
fluids. It regulates the volume and the concentrations of solutes in the cell. The
cell membrane also participates in the transmission of information to the cell and
contributes to its adhesion to neighbouring cells. It is 5 to 10nm thick and con-
sists principally of lipids and proteins that make up 80 to 90% of its weight. The
ratio of the weight of lipid to protein depends on the type of cell and the species,
but in animals is usually about 1 : 1. There are also some carbohydrates and water
present. The precise architectural arrangement of these constituents has been the
subject of speculation and argument for over a century. The lipids consist mainly
of phosphatidyl ethanolamine and phosphatidyl choline (lecithin), with smaller
amounts of phosphatidyl inositol and phosphatidyl serine. The lipid sterol cho-
lesterol is also present in animal cells. The phospholipids are amphipathic and

20
 Extracellular fluid Oligosaccharide
of glycoprotein \ ~·

Glycolipid l----

Cytoplasm

Fig.I.I. Depiction of the Singer-Nicolson "fluid mosaic" model of the cell (plasma) membrane.
Various protein components are distributed in a fluid phospholipid matrix. For further details
see the text

possess a hydrophilic phosphate "head" and a hydrocarbon "tail". In the presence

of water, the phospholipids aggregate to form bilayers with the heads facing the
water in an outwards direction while the opposing tails face inwards (Fig. 1.1). A
barrier lipid membrane is thus constituted which has a high permeability to other
lipids, a restricted permeability to water and similar-sized solutes, such as urea
and NH 3 , and which is virtually impermeable to large water-soluble molecules,
carbohydrates and ions. It has a natural lateral fluidity. Cholesterol increases
the density of the packing of the hydrocarbon chains and reduces fluidity and
permeability.
The arrangement and functions of the proteins in the cell membrane were
uncertain until about 30 years ago. Contemporary opinion then favoured the pres-
ence of bilateral protein layers that were thought to form a "sandwich" on either
side of the lipid. In 1972, Singer and Nicolson proposed that such proteins had
specialized functions and were distributed heterogeneously in the lipid matrix to
form a mosaic pattern. They were considered to be amphipathic, with their
hydrophobic face buried in the lipid and the hydrophilic one projecting into the
aqueous phase. In such situations they may span the membrane (transmembrane
proteins) or occupy peripheral sites. This fluid mosaic model of the cell mem-
brane is still current, but has been somewhat embellished. The specialized func-
tions of many of the constituent proteins have been uncovered. They include
the various solute transporters (channels, pumps and cotransporters) and water
channels (aquaporins), which have been described above. Also included are
specialized receptor molecules and their associated transduction proteins and

21
enzymes that are involved in cell-to-cell communication following interactions
with neurotransmitters and hormones. The cell membrane maintains functional
connections with the underlying microfilaments and microtubules of the cell
cytoskeleton network which helps to mediate such responses. It can also fuse with
vesicles formed from the endoplasmic reticulum and Golgi apparatus (exocyto-
sis). Such events occur in response to neural and hormonal signals.
The carbohydrates in cell membranes are usually present in oligosaccharide
chains that are part of glycoprotein and glycolipid molecules. They often carry an
electrical charge and project into the outer aqueous fluid. Substances such as
mucins are glycoproteins which contribute to the outer cell coat (glycocalyx).
The cell membrane is involved in the process of the adhesion to neighbouring
cells, from which they are separated by the intercellular or paracellular space. This
expanse contains the extracellular matrix consisting of macromolecules such as
polysaccharides and proteins, some of which are directly involved in cell adhe-
sion. The paracellular spaces also contain extracellular fluid and in barrier epithe-
lial membranes, such as the intestine and renal tubules, provide pathways through
which solutes and water may diffuse. Such molecular movements are greater in
"leaky" epithelia, such as the small intestine, than "tight" ones, such as the colon
and urinary bladder. The magnitude of such leaks depends on the presence and
integrity of tight junctions, which span and occlude part of the intercellular space.
They form part of the network of cell-cell adhesion processes, including the belt
desmosomes, which contain the protein actin. In epithelia, the tight junctions are
near the apical surface of the cells. Together with the adherins junction (of the
belt desmosomes) it forms the apical junction complex which contains the trans-
membrane protein occludin (Mitic and Anderson 1998). Synthesis of the proteins
making up the tight junction is a process that is regulated by the cell.

6.2 Capillaries

The capillaries are the small blood vessels that perfuse all tissues and constitute
the permeable barrier separating the fluids of the blood plasma and the intercel-
lular space. Solute, water and respiratory gas exchanges occur across the capil-
laries. They lie at the terminus of the arterioles and are contiguous with the
venules. They form a simple diffusion barrier lacking muscle attachments and
consist of a single layer of vascular endothelial cells lying on a supporting basal
lamina. Capillaries vary in their size and permeability characteristic depending
on the tissue where they are present. They are 0.1 to 1 mm long, 0.2 to 111m thick
with a diameter of 6 to 10 11m. (Erythrocytes, which are flexible, have a diameter
of about 71lm.) The permeability of the capillaries in the renal glomerulus is
about 1000 times greater than those in skeletal muscle. Such differences are
reflected in their structures. In muscle and skin the endothelial cells form a con-
tinuous layer, while in the glomerulus and intestine interruptions (fenestrations)
occur which are 20 to lOOnm wide. These gaps allow for greater molecular
exchanges. In liver and bone marrow the endothelial cell layer may be discontin-
uous and form sinusoids through which unrestricted movements of large mole-

22
cules, including proteins, may take place. Molecular exchanges across capillary
walls occur principally by simple diffusion with a smaller, but important compo-
nent due to bulk flow of water and its contained solutes (usually excluding plasma
proteins). The latter process occurs under the influence of the hydrostatic pres-
sure generated by the heart. (As it separates the larger protein molecules from the
remainder the process is referred to as ultrafiltration.) Diffusion of lipid-soluble
molecules occurs across the entire capillary surface, including the cell membranes
of the endothelial cells. Some water and ions may also follow this route, but it
appears to occur mainly through the fenestrations and pores in the endothelial
intercellular matrix. Bulk fluid flow due to hydrostatic forces occurs through pores
and fenestrations, which usually exclude the proteins. It is this process that prin-
cipally initiates and maintains the separate integrity of the volumes of the blood
plasma and intercellular fluids. It is called the Starling-filtration-reabsorption
process. It involves forces that are the algebraic sum of the hydrostatic pressure
and the osmotic pressure of the plasma proteins. In the proximal region of the
capillary, the hydrostatic pressure exceeds the osmotic pressure, and filtration
from the plasma to the intercellular fluid occurs. Distally, following a decline in
the hydrostatic pressure to levels less than that of the osmotic pressure of the
plasma proteins, fluid returns to the blood plasma. The balance of these forces is
normally well maintained, and even substantial changes in the blood pressure
have little effect. However, if there is a drop in plasma protein concentration, or
if a backpressure develops in the distal parts of the capillary, or permeability of
the capillaries change, excess fluid (oedema) may accumulate in the intercellular
spaces. Such changes can occur in such conditions as malnutrition, heart and
kidney disease, and capillary inflammation. There is little evidence to indicate the
presence of a general direct regulation of such processes, such as may be medi-
ated by nerves or hormones. However, in the kidneys of some species vascular
changes may influence filtration across the glomerulus and the formation of
urine.

6.3 Skin

The outer integument of vertebrates consists of the skin and in fishes and larval
amphibians also the gills. The skin forms a durable, relatively impermeable
barrier that protects the animal from adverse effects of the external environment,
including water and salt exchanges by diffusion and evaporation (Lillywhite and
Maderson 1982; Bereiter-Hahn et al. 1984; Toledo and Jared 1993). It is composed
of several layers of tissue including epithelial epidermal cells that are underlain
by a basal lamina and a layer of connective tissue called the dermis or corium.
The epidermis is in a continual and progressive state of development arising from
its basal stratum germinativum. Epidermal cells contain the fibrous protein
keratin, which eventually usually nearly fills the cells. They then die and become
the outer cornified layer of the skin, which is periodically replaced, along with
appendages such as scales, hair and feathers during shedding or moulting. The
low permeability of the epidermis principally depends on the presence of a lipid-

23
containing extracellular matrix. This structure seals the junctions between the
cells and reduces transcellular permeability.
The skins of different species of vertebrates have different permeabilities that
are usually consistent with their environmental lifestyles. In the sea and fresh
water the skin restricts the osmotic movements of water and diffusion of salts,
while on land evaporation is reduced. However, in amphibians the skin is gener-
ally much more permeable than in other vertebrates, which appears to reflect its
role in respiration.
The skin of different species of vertebrates contains various appendages, which
can modify the exchanges of water and salts. Glandular cells in the skin of fishes
and amphibians secrete mucins. Some frogs and toads that live in dry environ-
ments also secrete lipids from skin glands. They wipe this secretion over the skin
and thus reduce evaporation (Blaylock et al. 1976; Lillywhite et al. 1997). Most
birds possess uropygial (preening) glands near the base of the tail region. They
spread its secretion over the feathers to keep them flexible and waterproof. Many
mammals secrete a weak salt solution from sweat glands. It is evaporated to foster
cooling. The skin of some fishes contains chloride cells from which salt can be
secreted as an aid to their osmoregulation in sea-water (Marshall et al. 1997;
Yokota et al. 1997). As demonstrated by A. Krogh in 1937, the skin of frogs can
actively take up salt from fresh water. Amphibians also utilize their permeable
skin to aid their rehydration (cutaneous drinking) from pools of water or damp
soil.
Reptiles, birds and mammals usually possess, respectively, keratinous, and
often coloured, scales, feathers and hair, which can temper and reduce evapora-
tive water losses and heat gains from solar radiation. African reed frogs, Hyper-
olius viridiflavis, which can live for extended periods of time in exposed hot dry
environments, deposit small reflective plates made of guanine and hypoxanthine
in dermal iridophore (pigment) cells (Kobelt and Linsenmair 1992). They reflect
solar radiation and thus contribute to a restriction of the frog's heat gain and
evaporative water loss. Other frogs that live in arid environments may withdraw
to burrows during periods of drought and form enveloping cocoons composed
of sheets of epithelial cells which have been disposed of during moulting (Lee
and Mercer 1967; Withers 1995). Aestivation cocoons are also formed by African
lungfish when the waters in which they normally live dry up (Smith 1930a).

6.4 Water loss from the Tetrapod Respiratory Tract

Water loss from the lungs, bronchi, nasal passages and mouth takes place as a
result of gaseous exchanges that support metabolism and, in mammals and birds,
also a need for thermoregulatory cooling. Expired air is saturated with water
vapour due to evaporation from the pulmonary surfaces. If the inspired air has a
lower water vapour content, a net loss of water from the body will occur as a result
of such respiration. The water vapour concentration in the expired air is related
to the body temperature; at higher temperatures more water will be present. Some
small mammals and birds can reduce the temperature of the expired air and thus

24
save water. They have "cold noses" (Jackson and Schmidt-Nielsen 1964; Schmidt-
Nielsen et al. 1970}. Depending on the temperature and water content of the
inspired air, the relatively long narrow nasal passages of such animals can be
cooled due to heat loss to the incoming air and by local evaporation. The air
passing out over the colder nasal surface will then be cooled and lose water vapour
by condensation. The functioning of this counter-current heat exchanger depends
on the presence of long narrow nasal passages such as are often present in small
animals. In larger beasts, including humans, such an effect is small or absent.
Mammals and birds normally extract about Sml of oxygen from every 100ml of
inspired air prior to expiration, and this value does not normally vary signifi-
cantly.- However, some reptiles, such as aquatic diving species and desert lizards,
like the chuckwalla, Sauromalus obesus, have an irregular, discontinuous, pattern
of breathing. During such breath-holding, as much as 15ml of oxygen may be
extracted from lOOml of inspired air (Schmidt-Nielsen et al. 1966a; Thompson
and Withers 1997}. A considerable reduction in respiratory water loss may then
occur.
Many animals hibernate in winter, aestivate in hot dry summer periods and
periodically may go into states of torpor. Their body temperatures and rates of
oxygen consumption decline in such conditions (Storey and Storey 1990; Guppy
and Withers 1999}. Such metabolic depression, which may amount to as much as
SO% of the normal resting level, results in a decrease in pulmonary water loss.
Some small desert rodents appear to have a metabolic rate habitually lower than
predicted, which reduces their respiratory water loss (MacMillen and Lee 1970;
Rubal et al. 1995).
Evaporative cooling in response to increases in body temperature can occur
from the skin and respiratory tract. A rapid forced increase in pulmonary venti-
lation occurs in many species. It may be a shallow panting or in some birds a gular
flutter which results from rapid movements of the floor of the mouth and throat.
However, the need for such cooling can sometimes be delayed by allowing the
body temperature to rise by 2 to 7 °C, which may then approach lethal values. Such
controlled hyperthermia or heat storage has been observed in camels and desert
species of rodents and birds (Schmidt-Nielsen 1964a,b; Tieleman and Williams
1999). This accumulated heat may subsequently be dissipated during the night or
by periodic visits to cool burrows. A considerable reduction of the evaporative
loss of water can result from such behaviour.

6.5 Gills

Gills are primarily aquatic respiratory organs that are present in fishes and larval
amphibians. In fish they are the major interface with the fresh water or sea-water
in which they live. They make up about 90 to 95% of the total surface area of the
integument (Parry 1966}. The gills are permeable not only to respiratory gases
but also to water and solutes. The gills of fish are also the sites of H+ and HC03-
exchanges, which aid acid-base balance, the excretion of NH 3 and NH/ , which
contributes to their nitrogen metabolism, and for the exchanges of water, Na+ and

25
cl- that are involved in their osmoregulation. Fish gain water by osmosis across
their gills in fresh water, while in sea-water, depending on the osmotic concen-
trations of their body fluids, they either lose water in this manner, as seen in most
bony fish, or they may gain small amounts of water, as seen in cartilaginous fish
and hagfish. The gills are the site of a loss of salts by diffusion in fresh water and
a gain in sea-water. Fish in fresh water take up large amounts of water in this way.
The skin of fish has a relatively low permeability to water and salts and in fresh
water little drinking occurs (Lahlou et al. 1969a; Motais et al. 1969). Most of the
water uptake in freshwater fish occurs across the gills (Motais et al. 1969). The
gills are major sites of salt exchanges of fish in sea-water. Flounder, Platichthys
flesus, in sea-water can accumulate Na+ equivalent to about 40% of their total
exchangeable body Na+ each hour. About 75% of this uptake occurs across the
gills, the remainder being due to drinking (Motais and Maetz 1965). In fresh water,
flounder exchange less than 2% of their body Na+ each hour across their gills.
While the gills are the principal avenue for water and salt exchanges in fish, they
also provide a mechanism for compensating for water loss and salt gain in sea-
water and salt losses in fresh water. Apart from often being able to selectively limit
such water and salt exchanges that occur by diffusion, they are the site of mech-
anisms for the active uptake of salt in fresh water and its secretion in sea-water.
Such processes involve the activity of epithelial chloride cells in the gills. These
cells appear to be better developed in bony than in cartilaginous fish.
The morphology of the gills (Perry 1997; Evans et al. 1999) has been studied
most closely in teleost fish, but the general structural pattern appears to be similar
in other species. The respiratory and osmoregulatory epithelial cells are sup-
ported on the gill arches (or bars) which bear the gill filaments (also called
primary lamellae). The filaments bear numerous small parallel gill lamellae (also
called the secondary lamellae) that are the respiratory surfaces. The filaments
and lamellae are covered by epithelial cells, which are principally composed of
fiat pavement cells (also called squamous cells) that make up about 85 to 97%
of the total cells present. The remainder are principally mitochondria-rich cells,
which are the major site for the active ion exchanges and are thus also called iono-
cytes, chloride-secreting cells or, more commonly, chloride cells. Other types of
cells that are present include accessory cells, which abut the chloride cells, but
whose function is unknown, and mucous cells. The predominant pavement cells
are principally involved in respiratory functions, but they may also contribute to
exchanges of Wand HC0 3- and be sites of Na+ uptake (Gosset al. 1998). While
some chloride cells may be present on the lamellae, most are situated among the
epithelial cells that cover the interlamellar surfaces of the filaments. The inter-
cellular spaces of the paracellular pathways between the gill epithelial cells are
usually closed by tight junctions. However, in euryhaline fish adapted to sea-water
they expand and become leaky (Sardet et al. 1979). This change provides an
avenue for increases in the diffusion of solutes, including Na+. Mitochondria-rich
cells, which are thought to be functional chloride cells, have also been identified
in the gills of elasmobranch fish (Garcia Romeu and Masoni 1970; Laurent 1984),
lampreys (Morris and Pickering 1976; Peek and Youson 1979) and hagfish (Bartels
1985).

26
 Morphological changes occur in gill epithelia of fish during their transitional
adaptation from life in fresh water to sea-water (Conte and Lin 1967). Such
changes have been observed to involve the chloride cells. Apart from prolifera-
tion, there may be increases in their size, changes in the structure of their apical
cell membranes, increases in the concentrations of Na-K-ATPase on their baso-
lateral surfaces and modification of the intracellular tubular system. Two subtypes
of chloride cells (a and ~) have been identified in euryhaline fish (Pisam et al.
1987). The ~-type are present only in fresh water. The a-type, which has a dis-
tinctive apical plasma membrane and contains novel cytoplasmic inclusions, is
present on the gill filament near the base of the lamellae. It is thought to trans-
form into the marine type of chloride cell during adaptation to sea-water.
The gills have a complex vasculature (Laurent 1984; Nilsson and Sundin 1998)
which is consistent with their various functions. The lamellae receive blood from
the afferent branchial filamentous artery. The blood, on leaving through the
efferent filamentous branchial artery, may follow either of two pathways. It may
go directly to the systemic circulation or be "shunted" through an arteriovenous
pathway, called the filamentous nutritional vasculature, before entering the
central venous sinus. This shunt pathway principally supplies the filamentous
epithelium including the chloride cells. Control of the passage of blood through
the gills is under neural and hormonal control.
Movements of water and non-electrolytes by diffusion across the gills of fish
are generally quite restricted compared to those in other vertebrate epithelia
(Isaia 1984). For instance, in fresh water the permeability of the gills of rainbow
trout to water is less than 10% of that in the urinary bladder of a toad (The latter
is considered to be a "tight" epithelium!). The gills of elasmobranch fish have an
extremely low permeability to urea. It is 70 to 80 times less than that in rainbow
trout and eels, and 30 times less than that of the toad urinary bladder (Part et al.
1998). This property of the gills of elasmobranchs is consistent with their need to
retain urea for use as an osmolyte. The permeability of the gills of rainbow trout
and eels to water declines by about 50% following their transfer from sea-water
to fresh water. The mechanism for this effect is uncertain, but it could involve
morphological and vascular changes and, possibly, an alteration in the lipid com-
position of the cell membranes (Isaia 1984).
The gills of fish play a major role in maintaining the composition of their body
fluids in both fresh water and sea-water. Such activities, which have been most
closely examined in teleost fish, are interrelated to their role in acid-base balance.
In fresh water fish the gills can actively accumulate sodium chloride from the
external medium, while in sea-water they secrete the excess salt which is gained
by diffusion and as a result of drinking the medium. Such activities can be regu-
lated by processes that often involve the actions of hormones and growth factors.
The molecular mechanisms involved utilize many of the transporter proteins
which are summarized in Table 1.4. The include Na-K-ATPase, H+-ATPase, the
cotransporter Na+-K+-2cl-, ion exchangers (Na+/H+, cl-/HC03- and Na+/Na+), ion
channels (Cl-, Na+, and K+) and in elasmobranch fish gills, possibly a urea trans-
porter. Aquaporins could probably be utilized to advantage in fish gills but they
do not appear to have been investigated in this tissue. The sites and effects of

27
 Extracellular
Sea-water fluid
~ - - -Na•

L
cFTA·jY:g c1· 3 Na• ~IParacellular path

: \~~\~.
H20+C02 -
Carbonic J. 't - - - - ~ !S+- - -C02
anhydrase H CO Na•
2 3 ~ KCC_ "2CI"
Increased
by acidosis

Ct
K•

- - - - -
~
- - - NH: NH3

Fresh water

~ - - - - - - - - ~ - - NH3

Fig. 1.2. Summary of the processes of ion transport that occurs across the gills of teleost fish
in fresh water and sea-water. For further details see Table 1.4 and the text in Chapters 1 and 7

protein transporters in the gills of fish in fresh water and sea-water are summa-
rized in Fig. 1.2.

6.6 Gut

The gut, or alimentary canal, apart from being the site for digestion and absorp-
tion of nutrients, is also the principal avenue for the exchanges of water and
solutes in most vertebrates. The exceptions are fish and amphibians, which are
aquatic. The absorption of fluid from the gut involves not only that which is
imbibed but also a recycling of the considerable volumes that are secreted into
the lumen during the process of digestion. The gut contributes to the regulation
of the composition of the body fluids in several ways, which involve thirst, salt
appetite and the selective absorption of salts and water. These processes mainly

28
 occur across the small and large intestine (colon), and in marine teleosts, which
drink sea-water, the oesophagus. Additional such exchanges can occur across
intestinal caecae and the cloaca of reptiles and birds. Herbivorous species usually
have larger and longer guts than carnivores and can retain considerable volumes
of digesta and fluids in alimentary sacs, such as the rumen in cattle, sheep and
goats, the colon in horses and the caecum in rabbits. Such fluids are sometimes
considered to be part of the animal's extracellular fluids and may provide reser-
voirs that can buffer the process of dehydration.
The gut is lined by an absorptive and secretory tissue called the mucosa (Lacy
1991; Madara 1991; Chang and Rao 1994). It typically consists of a single layer
of columnar epithelial cells underlain by a basal lamina and a fibrous lamino
propria. The latter contains blood vessels and nerve fibres. The absorptive surface
of the intestine is increased by the presence of folds and villi, and microvilli (the
brush border) on the apical surface of its lining epithelial cells. In some species
of fish, including sharks, rays, chimaeras, sturgeons and lungfish, the intestinal
surface area is increased by the presence of the partitions that form a spiral valve.
The absorptive epithelial cells or enterocytes, cover the villi and new ones are
produced in the crypts, or wells, at their base. The crypts contain undifferentiated
epithelial cells, goblet cells, enteroendocrine cells and digestive Paneth cells. The
undifferentiated epithelial cells can function as secretory cells producing fluids
containing K+, cr- and HC0 3-. The epithelia can absorb fluids containing Na+, K+,
cl- and HC0 3- . Such processes involve the functional interactions of the cells
and the paracellular pathways which lie between them. Such a relationship may
provide the basis of a mechanism for the absorption of the considerable amounts
of fluid that occur across the intestine (Curran 1965; Spring 1999). The absorp-
tive and secretory processes that take place in the gut involve the activities of a
variety of transporter proteins and are summarized in Fig. 1.3.
Drinking can be regulated by the sensation of thirst, which usually reflects the
physiological need for water. A thirst centre, as well as a sodium appetite centre,
is present in the anterior diencephalon region of the brain. The hormone
angiotensin II (see Chap. 2) has a special role in initiating thirst and salt appetite
(Fitzsimons 1998). Drinking in response to the need for water occurs in all groups
of tetrapod vertebrates, with the notable exception of the Amphibia. The latter
instead take up water across their skin. Freshwater fish, which accumulate water
by osmosis across their gills, drink little. However, marine teleosts must drink sea-
water in order to maintain their bodily hydration. They imbibe fluid equivalent
to as much as 12% of their body weight each day (Motais and Maetz 1965). Elas-
mobranch fish apparently do not normally drink and, indeed, have little such
need, as their body fluids are maintained at concentrations which are slightly
hyperosmotic to sea-water. However, when injected with angiotensin II, drinking
can sometimes be induced in such fish (Hazon et al. 1989). The drinking of sea-
water by teleosts involves a considerable adjustment by the fish, as this solution
is about three times as concentrated as their body fluids. Ultimately, as described
above, the excess salt is rapidly excreted as a result of the secretory activities of
the chloride cells in the gills. The absorptive process for the imbibed sea-water
involves an uptake of the sodium chloride and accompanying water, mainly across
the wall of the oesophagus. The process involves diffusion and an active coupled

29
Lumen Apical Basoiaterai Interstitium
membrane membrane
N~ ~------~3~N~a~.-~~
Glucose~
Amino a c i < * HCO _ :a12
A
K•

Na'
~trct :~~
·~ Small intestine

,p
1

~.{1. c·FTR-type _ 4- $~
? Na• K• 2 Ci"
Cl- secretory
pathway in
crypt cells
Cl- - - - - - - ·- - - - ~

ActiveK•&
Cl· absorption ?

Colon

c1· and K•
secretory
pathway in
crypt cells

Fig. 1.3. Summary of the various transport mechanisms involved in the absorption and secre-
tion of solutes across the small intestine and colon. Most of the information has been derived
from observations in mammals, but such processes have also been identified in the other
phyletic groups. For further details and references see Table 1.4 and the text

absorption of the Na+ and cl- (Hirano and Mayer-Gostan 1976; Nagashima and
Ando 1994).
The colon, or large intestine, has a special role in regulating water, Na+ and K+
excretion in the faeces. There is a selective absorption of fluids and Na+, and a
secretion of K+. The absorption of Na+ involves the activity of special epithelial
sodium channels (ENaC, see Table 1.4), which are also found in kidney tubules,
amphibian skin and urinary bladder, but not usually in other regions of the gut.
The ENaC can be specifically inhibited by the drug amiloride and have been iden-
tified in this way in the colons of amphibians, reptiles, birds and mammals, but
apparently not in fishes. The intestinal contents can undergo considerable dehy-
dration in the colon, where the water content may decline from about 95% in the
small intestine to 60 to 70% in the faeces. It has been proposed that this fluid
absorption occurs from the crypts at the base of the villi. A local osmotic gradi-
ent appears to be established across the mucosal membrane at this site as a result

30
of active Na+ transport (Naftalin and Pedley 1999; Naftalin et al. 1999). This con-
centration gradient is maintained due to the presence of a pericryptal sheath,
which prevents dissipation of the Na+ into the submucosal tissue. The osmotic
pressure across the cryptal mucosal membrane is transduced into a suction
hydrostatic pressure in the crypts. This pressure appears to be sufficient to remove
fluid from the colonic contents. The pericryptal membrane has been functionally
and microscopically identified in the rat distal colon.
The alimentary tract in non-mammals usually terminates in a cloaca, which it
shares with the ureters and reproductive ducts. The cloaca can be quite large and
the site of active Na+ absorption in birds and reptiles (Bentley and Schmidt-
Nielsen 1965; Skadhauge 1967). In birds, a reflux of urine into the upper regions
of the colon has been demonstrated, providing an opportunity for further reab-
sorption of urinary water (Akester et al. 1967; Nechay et al.1968). Schmidt-Nielsen
and his collaborators (Schmidt-Nielsen et al. 1963) suggested that in some rep-
tiles and birds, salt reabsorbed from the cloaca may be subsequently excreted by
the nasal salt glands (see later). As the salt concentrations in the nasal gland secre-
tions are much higher than those in the urine, a reduced urinary water loss may
thus be accomplished. The physiological reality of this ingenious suggestion
remains to be proven to the satisfaction of all (Thomas 1997).

6.7 Urinary Bladder

Fluid stored in the urinary bladder can make important contributions to the
osmoregulation of some vertebrates. Urinary bladders are present in many, but
not all, species. In fish they are usually quite small and are derived embryonically
from mesoderm. They are expansions of the mesonephric ducts. In tetrapods the
urinary bladder originates as an endodermal evagination of the cloaca. These
urinary bladders can be quite large and in some amphibians can hold fluid equiv-
alent to about 50% of their body weight. Tortoises also may have a capacious
urinary bladder holding fluid equal to 20 to 30% of their body weight. Birds, croc-
odiles, alligators, snakes and most lizards lack such a urinary bladder. The urinary
bladder can be quite permeable to water and is often the site of an active reab-
sorption of Na+ and/or cr-. Its permeability and ion transport properties reflect
the presence of a lining of epithelial cells, which in fish consists principally of
mitochondria-rich cells. These cells are also present in other species but may be
interspersed with other types of cells such as "granular" cells in amphibians. The
mammalian urinary bladder, which is often exposed to urine with a hyperosmotic
concentration, is relatively impermeable and has a multilayered epithelial lining.
In amphibians and tortoises, water stored in the urinary bladder can be reab-
sorbed or provide a storage site for solutes during dehydration (Bentley 1966; ]0r-
genson 1998). Fluid can also be conserved by its reabsorption from the bladders
of marine teleost fish (Howe and Gutknecht 1978). An active reabsorption of Na+
and cr- may result in a physiologically significant conservation of salt in fresh-
water fish (Curtis and Wood 1991) and probably also amphibians (Bentley 1966)
and chelonian reptiles (Brodsky and Schilb 1960). Ion transport and the control

31
of water permeability have been studied in urinary bladders under in vitro con-
ditions. In teleost fish a linked Na+-cl- absorptive process has been identified
(Lahlou 1967; Lahlou and Fossat 1971; Renfro 1975). The studies on winter floun-
der by Renfro provided the first genetic material for the cloning (Gamba et al.
1993) of the Na+ -cl- co transport protein (Table 1.4). This protein also mediates
ion transport in the distal convoluted renal tubule of mammals. In frogs and toads
the urinary bladder has been widely used to study the process of active transep-
ithelial Na+ transport (Leaf et al. 1958), and hormonally regulated osmotic water
permeability and Na+ transport (Bentley 1958; Crabbe 1961a,b). It also provided
a preparation for the early studies of amiloride-inhibitable Na+ transport (medi-
ated by ENaC) in epithelia (Bentley 1968).

6.8 Salt Glands

Many birds, reptiles and elasmobranch fish possess salt-secreting glands that can
often produce hyperosmotic solutions, which principally contain either sodium
chloride or potassium chloride. The concentrations of these solutions are much
greater than can be achieved in the urine of such animals (Table 1.5). The salt
glands are used to excrete excesses of ions, which are obtained in the diet, as a
result of drinking sea-water or by diffusion across the gills. The relative develop-
ment of these tissues usually reflects the animal's exposure to such regimens and
conditions.

Table 1.5. Sodium and potassium concentrations in extra-renal salt glands in vertebrates

mEql~ 1

Na• K+

Chondrichthyes-rectal gland
Spiny dogfish' (Squalus acanthias) 540 7
Reptilia
Chelonia-supraorbital "tear" glands
Loggerhead turtleb (Carretta carretta) 732-878 18-31
Lacertilia-lateral nasal gland
Desert iguana' (Dipsosaurus dorsalis) 494 1387
Marine iguanad (Amblyrhynchus crisatus) 1434 235
Ophidia-sublingual gland
Sea snake• (Aipysurus /aevis) 798 28
Crocodilia-lingual gland
Estuarine crocodiler (Crocodylus porosus) 386-740 10-16
Birds-supraorbital nasal gland
Herring gullg (Larus argentatus) 718 24
Leach's petrelg (Oceanodroma leucorhea) 900-1100
Mallard duckg (Anas playrhynchos) 550

' Burger and Hess (1960). b Holmes and McBean (1964). ' Schmidt-Nielsen et a!. (1963).
d Dunson (1969). • Dunson and Dunson (1974). r Taplin (1988). g Schmidt-Nielsen (1960).

32
 Salt glands are derived embryonically from a variety of glands including tear
glands in turtles, nasal glands in birds and lizards and salivary glands in some
snakes. Morphologically they are similar and consist of a system of branched
secretory tubules that open into a series of ducts. In elasmobranchs a central duct
empties into the rectal region of the gut. (Hence this gland is called the rectal
gland.) In birds and lizards this duct opens into the nasal cavity, while in sea
snakes and crocodiles it opens into the mouth. All such salt glands appear to share
a common mechanism for forming their secretions, which is similar to that of the
chloride cells in fish (Fig. 1.2). Chloride is secreted actively across the apical side
of the tubular cells following its entry, utilizing the Na+-K+-2cl- cotransporter,
across the basolateral surface of the cell. The initial genetic cloning of this latter
transport protein was accomplished using tissue from the rectal gland of the spiny
dogfish (Xu et al. 1994). Sodium ions appear to follow the Cl- by diffusion, along
paracellular pathways down the established transepithelial electrochemical gra-
dient. The secretory cells are rich in mitochondria and have high concentrations
of Na-K-ATPase on their basolateral surfaces (Shuttleworth and Hildebrant 1999;
Silva et al. 1999a).
The secretory activity of the salt glands of sea birds and turtles was discovered
by Knut Schmidt-Nielsen and his collaborators in 1958 (Schmidt-Nielsen and
Fange 1958; Schmidt-Nielsen et al. 1958; Schmidt-Nielsen 1960). In 1960, Burger
and Hess described the functioning of the rectal gland in the spiny dogfish.
Shortly afterwards, the salt -secreting function of nasal glands was described in
several species of lizards (Schmidt-Nielsen et al. 1963; Templeton 1964). The secre-
tions formed by the lizard's salt glands differed from those of the other species
as they often contained high concentrations of potassium chloride instead of
sodium chloride. The ability to secrete a concentrated potassium chloride solu-
tion was also observed in the marine iguana from the Galapagos Islands (Dunson
1969). The secretion of K+ apparently occurs in response to the needs of reptiles
that consume herbivorous diets, which contain large amounts of potassium. If
potassium chloride solutions are given to ducks, the composition of their salt
gland secretion is unchanged and the excess K+ is then excreted in the urine
(Simon and Gray 1991). The mechanism of this special ability of some reptile salt
glands to secrete K+-rich solutions is unknown.
Salt glands can secrete relatively large volumes of fluid. In herring gulls this
volume can be ten times as great per gram of tissue as that occurring in the human
kidney (Schmidt-Nielsen 1960). In birds the secretory response is initiated by a
rise in the plasma osmotic pressure and increases in the plasma volume. It is
mediated by neural stimuli arising from the parasympathetic nervous system.
Acetylcholine is the principal neurotransmitter. Rectal gland secretion occurs in
response to increases in plasma volume and may involve local nerve network, but
hormonal stimulation (by a natriuretic peptide hormone) appears to be the pre-
dominant mediator (Valentich et al. 1995). Potassium secretion by the nasal salt
glands in lizards can be initiated by the injection of potassium chloride (Shuttle-
worth et al. 1987). Both nerves and hormones could be involved in this process,
but the details, including those of the secretory process in the cells, are unknown.
It is possible that K+diffuses down electrochemical gradients via activated potas-
sium channels in the apical plasma membrane.

33
 The use of salt glands to secrete excess electrolytes appears to be an ancient
process in vertebrates. Evidence for the presence of nasal salt glands has been
found in fossil dinosaurs belonging to the order Ornithischia (Whybron 1981).
These reptiles were apparently related to birds (they had a bird-like pelvis) and
were herbivorous. Possibly these salt glands secreted a K+-rich fluid, though that
would not have been bird-like!

6.9 The Kidneys

Kidneys play a major role in the osmoregulation of vertebrates. However, their

particular functions differ depending on the animal's phylogeny and whether it
habitually lives in fresh water, the sea or terrestrial environments, such as deserts
or more temperate regions. The particular physiological roles of kidneys are also
related to the presence of other tissues and organs, which can contribute to
osmoregulation, including gills, salt glands, the skin of amphibians and a reab-
sorptive urinary bladder. General references include Dantzler ( 1992 ); Jamison and
Gehrig (1992); Vander (1995); Braun and Dantzler (1997) and Reilly and Ellison
(2000).

6.9.1 Functions

The primary role of the kidneys is to maintain the constancy of the composi-
tion of the extracellular fluids. This function includes the volume, concentrations
of mineral ions (Na+, K+, Ct, Ca2+ and Mg2+) and acid-base balance (H+ and
Hcon. The kidney also contributes to the excretion of endogenous metabolites,
such as result from nitrogen metabolism (NH 3, urea and uric acid). The processes
of the excretion of excesses of water and solutes also involves a concur-
rent conservation and retention of essential constituents of the body fluids.
The kidney also functions as an endocrine organ (see Chapter 2) and can
secrete hormones and growth factors, including renin, erythropoietin and
1,25-dihydroxyvitamin D3•

6. 9.2 Structure

The intimate structure of the kidney varies in different species and is related to
such factors as their phylogeny, body size and habitual physiological needs. The
basic functional tissue unit in the kidney is the nephron. Each kidney contains
many thousands, even millions, of such units. The numbers generally reflect the
animal's size and metabolic rate. Nephrons are arranged in orderly arrays in rela-
tion to each other and the blood vessels that supply them. The latter arise from
the renal artery or often in non-mammals from a venous renal portal system.
Groups of nephrons may be arranged in the kidney in distinct lobules and zones,

34
which may be situated centrally or peripherally. In mammals and birds they are
present in an outer cortex and an inner medulla and papilla.
The basic architecture of the nephron includes a capillary bed called the
glomerulus, which is surrounded by the Bowman's capsule. The latter connects
with a morphologically and functionally segmented tubule lined by epithelial
cells. The principal segments that are present vary in different species but often
consist of a "neck" segment followed by the proximal tubule, intermediate seg-
ment, distal tubule, connecting duct and collecting ducts. Various smaller seg-
ments have also often been defined, especially in mammals. The morphological
and physiological characteristics of the lining epithelial cells usually differ in the
various segments. They are the sites of various arrays of transport proteins (Table
1.4; Fig. 1.4). The glomeruli are supplied with arterial blood which passes in
through an afferent and out through an efferent glomerular arteriole. The latter
can then break up into capillaries, which supply the tubules. Alternatively, in
mammals and birds the efferent arterioles from some nephrons (juxtamedullary
nephrons) send long capillary vessels deep into the renal medulla and papilla (the
vasae recta) where they form hairpin bends, or loops, before returning to the
renal vein. The venous renal portal system from the tail region of non-mammals
supplies only the renal tubules. The afferent glomerular arterioles are the site of
two local regulatory mechanisms: baroreceptors and the macula densa. The latter
consists of a group of columnar epithelial cells, which in mammals adhere to
part of the adjacent distal renal tubule. There are many interspecific variations of
the basic structure of the nephron. Not all vertebrates have glomeruli at all. They
can be reduced in number or even completely absent (aglomerular) in many
species of marine fish and even in some snakes. On the other hand, hagfish (class
Myxini, primitive jawless fish) lack nephrons (anephric) but possess large
glomeruli that open directly into the archinephric duct. A distal tubule (the dilut-
ing segment) is absent in most marine teleost fishes but is present in most such
freshwater and euryhaline species. Marine, but not freshwater, elasmobranch fish
possess very long nephrons that are arranged to form two hairpin loops with each
other and associated blood vessels. A countercurrent flow system appears to be
formed which is comparable to that present in mammals and birds (Friedman
and Hebert 1990). It has been suggested that this system may contribute to
the kidney's ability to conserve urea in these fish (Boylan 1972). In birds and
mammals the proximal and distal tubules are joined by an elongated thin inter-
mediate tubule which also forms a hairpin bend, or loop, which may extend deep
into the renal medulla and papilla. The entire looped structure of the nephron is
called the loop of Henle and includes part of the proximal and distal tubules. This
region of the latter is called the thick ascending limb of the loop of Henle. The
loop of Henle lies parallel to the blood vessels of the vasa rectae and provides the
countercurrent flow system that allows mammals and birds to secrete a hyperos-
motic urine (Table 1.6). The countercurrent flows of blood and glomerular filtrate
preserve the high concentrations of osmolytes which accumulate in the renal
medullary tissue and provide the concentration gradients necessary for the for-
mation of a hyperosmotic urine. This system is generally not as well developed
in birds as in mammals.

35
Table 1.6. Maximum urine concentrations of various species of
mammals and birds

mosmoll- 1

Mammals
Humans' 1450
Mountain beaverb (Aplodontia rufa) 500
Seal' (Phoca vitulina) 2200
Sand ratd (Psammomys obesus) 6300
Spinifex hoppin~ mouse' (Notomys alexis) 9400
Quokka wallaby' (Setonix brachyurus) 2200
Echidna8 (Tachyglossus aculeatus) 2300

Birds
Domestic fowlh (Gallus domesticus) 520
Emu' (Dromaius novae-hollandiae) 485
Ostrich; (Struthio camelus) 800
Budgerygahk (Melopsittacus undulates) 850
Zebra finch' (Taeniopygia castanotis) 1005

' Smith (1951). b Dicker and Eggleton (1964). ' Smith (1936).
d Schmidt-Nielsen (1964a). ' MacMillen and Lee (1969).
r Bentley (1955). 8 Bentley and Schmidt-Nielsen (1967).
h Skadhauge (1981). 1 Skadhauge (1974). i Withers (1983).
k Krag and Skadhauge (1972).

6. 9.3 Physiology

The formation of urine begins with the ultrafiltration of plasma across the cap-
illaries of the glomerulus. This ultrafiltrate contains electrolytes and small solutes
with a similar concentration to that of the plasma, but little or no protein. In
humans about 120ml of plasma are filtered in this way each minute. It is called
the glomerular filtration rate or GFR. The urine flow in humans is only about
1 ml each minute so that about 99% of this filtrate is reabsorbed as it passes along
the renal tubule. The GFR varies widely in different species reflecting their body
size, metabolic rate and their environmental circumstances. In humans the
GFR (mlkg- 1 h- 1) is about 100, while in rats it is 200 and in domestic fowl 75.
In terrestrial reptiles it varies from about 4 to 25 mlkg- 1 h- 1 and it is reduced
when the animals are dehydrated (Dantzler 1992}. In fresh water the GFR is about
34mlkg- 1 h- 1 in frogs and 9mlkg- 1 h- 1 in rainbow trout. When these trout are
adapted to sea-water, the GFR decreases to about 1 mlkg- 1 h- 1•
A reabsorption of filtered water and solutes occurs progressively as the filtrate
passes along the nephron. The process involves the activities of the renal tubular
epithelial cells and a variety of their transporter proteins (Fig. 1.4). Other solutes
may be added as a result of the secretory activities of the renal tubular epithe-
lium. Such substances that are secreted include K+, H+, NH 3 and uric acid. In
aglomerular fish, sodium chloride and water are secreted across the proximal
tubule.

36
 Lumen Basolateral Apical Interstitium
membrane membrane
3 Na•

Proximal
tubule

Na• 3 Na•
2CI·
K• 2 K• Thick
K•
Fluid
Na• ascending
hyposmotic H• limb of Henle's
ROrK
loop
K•
Na•
HC03
----~

~
Distal
convoluted
cr K+ K• > .. 2 K•
tubule
::=:r::-
C I" Klr

Fig. 1.4. Summary of the various transport mechanisms that are involved in the formation of
urine by the kidney. Most of the information refers to the mammalian kidney, but homologous
mechanisms have been identified in other vertebrates. For further details and references see
Table 1.4 and the text

In mammals, about 65% of the glomerular filtrate, including all the glucose and
most of the HC0 3- are usually reabsorbed in the proximal tubule. This fluid
remains isosmotic to the plasma due to its osmotic equilibration, with the aid of
aquaporins. The distal tubule is referred to as the diluting segment since, follow-
ing further reabsorption of Na+ and Cl-, the luminal fluid becomes hyposmotic
due to its low permeability to water. In mammals the diluting segment is usually
considered to be part of the thick ascending loop of Henle and the distal convo-
luted tubule. About 25% of the Na• and Cl-, and the remainder of the K+ in the
filtrate are reabsorbed in this part of the nephron. The process involves the activ-
ities of the Na•-K•-zcl- and the Na•-cl- cotransporter proteins. The late distal
tubule and the collecting ducts are the sites of the final regulated reabsorption of
Na•. This process utilizes specific epithelial sodium channels (ENaC). A secretion

37
of K+ also occurs in the distal tubules, as well as adjustments of the pH involving
a secretion of H+ and NH 3• In mammals, and possibly some other tetrapods, the
transport of Na+ and K+ in this region of the nephron can be regulated by the
hormone aldosterone. This region of the nephron is usually quite impermeable
to water. However, under the influence of antidiuretic hormone (ADH) and aqua-
porin 2 its permeability can increase, allowing an osmotic equilibration of the fil-
trate with the hyperosmotic fluids which, in mammals and birds, are present in
the renal medullary tissue. A hyperosmotic urine can thus be formed in such
species.

6.9.4 Regulation

The regulation of the secretion of urine involves hormones and nerves and
autoregulation, which arises from within the kidney itself. Such control mecha-
nisms can influence the GFR and absorption and secretion across the renal tubule.
The hormones usually are produced by the endocrine glands but "local"
hormones produced by the kidney tissue can also contribute to regulation. The
neural mechanisms are generally mediated by a sympathetic nerve supply to the
glomeruli and renal tubules (DiBona and Kopp 1997; DiBona 2000). Local hor-
mones include the products of arachidonic acid metabolism, such as
prostaglandins, nitric oxide, dopamine and kinins. Hormones produced by
endocrine glands that exert direct effects on kidney function include vasopressin
(antidiuretic hormone, ADH), vasotocin, aldosterone, natriuretic peptides
and angiotensin II. These hormones will be described in succeeding chapters.
Glomerular function is usually well controlled by the vascular activity of the affer-
ent and, sometimes, the efferent glomerular arterioles. The rate of filtration across
single, individual, glomeruli normally changes little. However, large changes in
the GFR frequently occur in non-mammalian vertebrates, and this process usually
involves increases or decreases in the numbers of the functioning glomeruli
(glomerular intermittency or recruitment). In individual nephrons an equilib-
rium usually exists between the GFR and rates of tubular reabsorption. This rela-
tionship is sometimes referred to as glomerular-tubular balance. The rate of
delivery of water and solutes to the tubule is related to the GFR and their con-
centrations in the plasma. If, for instance, delivery is increased, the normal reab-
sorptive processes may tend to reject the excess, which will then be excreted in
the urine. Such an effect is seen dramatically in the disease of diabetes mellitus,
when an increased delivery of plasma glucose to the renal tubule results in its
appearance in the urine. The excretion of Na+ and urea can be similarly influ-
enced locally in the kidney due to a situation that has been called glomerular
tubular imbalance. Conditions in the renal tubule can also influence the GFR. This
process of tubuloglomerular feedback results from the ability of the macula densa
cells to monitor the concentrations of sodium chloride present in the filtrate and
convey this information back to the afferent glomerular arteriole. Small, appro-
priate, changes in the GFR can then be induced. Such autoregulatory processes
are clearly important for the regulation of kidney function. Nevertheless, an

38
absence or excess of hormonal regulation can have disastrous effects on kidney
functioning, as seen in several human and animal diseases.

7 Relationships of Nitrogen Metabolism to Osmoregulation

Proteins can be converted to carbohydrates and lipids, and also provide precur-
sors for nucleic acids. This process involves breakdown to their constituent amino
acids, which undergo oxidative deamination resulting in the release of a-amino
nitrogen and the formation of ammonia (NH 3 ) (Fig. 1.5). This NH 3 is highly toxic,
especially to the nervous system. In rabbits a concentration of 0.03 mmoll- 1 is
fatal. The NH 3 is readily diffusible in water so that vertebrates that live in aquatic
environments can excrete it directly into their bathing solutions. Ammonia is
readily converted to ammonium (NH/) at a physiological pH, and much of it
usually exists in this form. Ammonium is also water-soluble but it is less lipid-
soluble than NH 3 and hence is less toxic. Excretion occurs across the gills of bony
and agnathan fish and the skin of larval forms of amphibians. As this process is
the predominant manner in which they excrete waste nitrogen, they are said to
be ammonotelic (also called ammoniotelic). Ammonia can be formed from glu-
tamate in the distal renal tubule, where its secretion results in the neutralization

Dietary issue proteins

-1
'i
a - amino acids
a- ketoglutarate transaminase enzymes
Ornithine-urea Oxidative
glutamate+ a· keto acid
cycle
(Uver mitochondria)
of the amino acid deamlnatlon
carbamyl phosphate t;:tamine dehydrogenase

y
synlhetaH I
CPS I 2ATP HCO;
./ ./ NH4+ a- ketoglutarate Excretion
carbamoyl ( L ~ Gills of bony fish, agnathans,
phosphate Mammals, some amphibian skin, urine
·. 1 I".. reptiles, amphibians, glutamate
orntthine---T,j,- lungfish ATP NH 4+

aspartate 4
citrulline

argmme
.
~HCO
2ATP
3
-............._
glutamine
1
glutammesynthetase71
~
glutammase
L... 7 11 1
guamae

CPS Ill oxidative deammation

ornithine ~ argmase Elasmobranchs, ' . of amino acids

Retention
/
UREA'
\
"""--
~xcr~tlon
coelacanth
(embryontc
teieosts?)
l
a- ammo nttrogen

Osmolyte '" urme Excretion purinj synthesis ---7 ~~~~=i~e

Elaamobranchs, In urine: W
Storage
crab-eating frog,
coelacanth, renal Aestivating amphibians
birds, most -----,
reptiles,some I I
hypoxanthine
uricase
medulla mammals and lungfish amphibians URIC ACID ·( > allantoln

Fig. 1.5. Summary of the pathways of nitrogen metabolism and their phyletic distribution in
vertebrates. General references are: Anderson (1995); Wright (1995); Campbell et a!. (1987);
Walsh (1997); Withers (1998b)

39
of H+ to form NH/, which is excreted in the urine. This process helps maintain
the pH of the urine at physiologically acceptable levels. The NH/ also can sub-
stitute for Na+, which is reabsorbed, and would otherwise be excreted in exces-
sive amounts. Some tetrapod vertebrates with a surfeit of available water excrete
large amounts of NH/ in their urine and have been described as exhibiting fac-
ultative ammonotelism and include crocodilians and, remarkably, humming birds
(Preest and Beuchat 1997). However, tetrapod vertebrates, as well as some fish,
especially elasmobranchs, resort to other strategies to detoxify NH 3• Some convert
it to urea and others to uric acid. Such species are said to be, respectively, ureotelic
and uricotelic. There are no clear phyletic distinctions as to which groups of ver-
tebrates utilize a particular process for nitrogen excretion nor are they mutually
exclusive. Ammonotelic fish often also excrete small amounts of urea, while croc-
odiles excrete both ammonia and uric acid. Turtles and tortoises can excrete both
urea and uric acid. Hence the prefix "mainly" is often used. Mammals and amphib-
ians are then described as being mainly ureotelic while birds and most reptiles
are mainly uricotelic. Elasmobranch fish, the coelacanth, Latimeria, and the crab-
eating frog, Rana cancrivora, retain urea and utilize it as a retention osmolye to
maintain the osmotic concentrations of their body fluids similar to that of their
environmental sea-water. They are described as being ureosmotic, though they
appear to be also ureotelic.
Urea is very water-soluble and appears to principally cross cell membranes by
passing along paracellular pathways and by utilizing special urea transporter pro-
teins in cell membranes (see Table 1.4). It has a low toxicity and in some ure-
osmotic species possible toxic effects may be reduced, as described above, by the
presence of counteracting solutes such as methylamine compounds. Urea can be
readily excreted in the urine, though a retention mechanism exists in the kidneys
of ureosmotic species and in the renal medullary tissue of mammals. Uric acid
contains four nitrogen atoms compared to two in urea. Uric acid is quite insolu-
ble but remains in solution in the renal tubule. However, in birds and reptiles it
is subsequently precipitated in the cloaca, where a reabsorption of urinary water
occurs. The excretion of nitrogen as uric acid in the urine requires less water than
when urea is utilized as the end product of such metabolism. It has been esti-
mated that 1 g of nitrogen requires 10 ml of water for its excretion in uricotelic
animals as compared to 10 to 50 ml in ureotelic species and 500 ml in ammonotelic
ones (Smith 1951). It has been suggested that the savings of water that occur as a
result of uricotelism were a major factor in the success of the archosaurian "ruling
reptiles", which included the dinosaurs and ancestors of the birds (Campbell
et al. 1987). The ornithine-urea cycle appears to have been a requisite for the
movement of the Amphibia onto dry land, and they may have inherited this ability
from crossopterygian relatives. Extant ancestors of the latter are the coelacanth
and lungfish, which can synthesize urea.
A number of vertebrates, which live under osmotically stressful conditions,
have been observed to modify the habitude of their nitrogen metabolism. African
lungfish are normally ammonotelic but when they experience periods of drought
and aestivate they synthesize urea. This metabolite is accumulated in their body
fluids at concentrations that may be as high as SOOmmoll- 1 (Smith 1930a). A
similar storage of urea, at concentrations in the body fluids up to 900 mmoll-I,

40
has been observed in some frogs and toads that live in deserts (McClanahan 1967;
Degnani et al. 1984; Withers and Guppy 1996). Even more remarkable was the
discovery of several species of tree frogs from Africa and South America (genera
Chiromantis and Phyllomedusa) which are uricotelic (Loveridge 1970; Shoemaker
et al. 1972a; Drewes et al. 1977). African reed frogs, Hyperolius viridijlavus, which
live in dry exposed situations, are ureotelic (Schmuck et al. 1988). As described
above, they can deposit platelets that reflect sunlight in their dermal iridophores.
These platelets are composed of the purine compounds guanine and hypoxan-
thine derived from the metabolic nucleic acid-uric acid pathway. Formation of
these platelets continues in dry periods, when it apparently provides a "sink" for
waste nitrogen, thus reducing the need to synthesize urea.
The biosynthetic pathways that mediate the synthesis ofNH 4+ are summarized
in Fig. 1.5. The synthesis of urea involves the formation of carbamoyl phosphate
which enters the ornithine-urea cycle. This synthesis is mediated by the enzyme
carbamoyl phosphate synthetase (CPS). Elasmobranch fish and the coelacanth
possess a variant of this enzyme called CPS III, while that in mammals, amphib-
ians and chelonian reptiles and lungfish is CPS I. Some embryonic teleost fish
possess CPS III, but few adult teleosts utilize the ornithine-urea cycle. However,
it appears that the requisite genes may still be present in these fish. Uric acid is
also a waste product of nucleic acid metabolism, but in most ureotelic species it
is converted to allantoin by uricase. However, this enzyme is not present in uri-
cotelic species or higher primates such as humans. Nucleic acid synthesis utilizes
a-amino nitrogen to form purine and pyrimidine nucleotides. The purine
pathway has apparently been coopted by uricotelic species for more general use
in disposing of a-amino nitrogen as uric acid. Urea can also be formed from uric
acid, and this process can occur in some teleost fish.

8 Osmoregulation and the Evolution of Vertebrates

The nature of the processes of osmoregulation in extant vertebrates has provided
the basis for some stimulating speculation about their origins and evolution.
Extrapolations to the physiological nature of osmoregulation in early vertebrates
may be relevant to questions such as their possible origins in fresh water or the
sea, and if tetrapods arose from freshwater or marine ancestors. Fossils from the
Palaeozoic era have provided morphological evidence regarding the distribution
of the various phyletic groups in geological time and the nature of their envi-
ronments. However, such information is often difficult to interpret. It is generally
agreed that the vertebrates evolved from a protochordate, which may have been
a cephalochordate (Chen et al. 1995) related to amphioxus (Branchiostoma). All
known protochordates live in the sea. The earliest vertebrates were jawless fish
(superclass Agnatha, the cyclostomes) the fossils of which (ostracoderms) first
appeared in the Ordovician period about 500 million years ago. Contemporary
agnathans, hagfish and lampreys, are, respectively, exclusively marine and eury-
haline. Like most other fish, their kidney function involves the presence of
glomeruli. As these structures are well suited to the excretion of excess water, it

41
has been suggested that their presence reflects the evolution of such fish from a
freshwater ancestor (Marshall and Smith 1930; Romer 1955). However, this expla-
nation has not been accepted by all (Robertson 1957; Halstead 1985; Griffith
1987). It is now generally agreed that the geological sediments where the first fossil
agnathan remains were discovered were marine. Furthermore, glomerular-like
vascular structures also function as excretory organs in marine invertebrates that
have no freshwater lineage. Their roles in marine vertebrates, including hagfish,
appear to be related to the regulation of ion, rather than water, concentrations in
the body. The presence of glomeruli and their use for the excretion of excess water
could be considered to have arisen as a preadaptation, which was subsequently
utilized by a freshwater ancestor.
Hagfish (superclass Agnatha; class Myxini; order Myxiniformes) are consid-
ered to be extant relatives of fossil agnathans that are collectively described as
ostracoderms (class Pteraspidomorphi; order Heterostraci and others). They are
exclusively marine and the composition of their extracellular body fluids, except
for divalent ions, is remarkably similar to that of sea-water (Table 1.2). The diva-
lent ions are present in higher concentrations than in sea-water and are, appar-
ently, mainly excreted by the kidney. However, intracellular concentrations of ions
in hagfish are similar to those in other vertebrates and are much lower than those
in the extracellular fluid (Table 1.3). Osmotic balance is achieved by utilizing
amino acids as intracellular osmolytes. Hagfish are now often considered to
provide an osmotic prototype for the first vertebrates. (The Agnatha are consid-
ered to be a diphyletic group with the lampreys, class Petromyzontiformes, dis-
playing the clearest affinities to contemporary vertebrates (Bardack and Zangerl
1968).) The ancestral chondrichthyean fish appear to have been marine, like most
extant species, and presumably utilized urea as an osmolyte to allow for a decrease
in the concentrations of ions in the body fluids. Such ion concentrations may have
been advantageous with respect to the stability and functioning of cell macro-
molecules. The maintenance of isosmoticity between the body fluids and
the bathing sea-water may also have been energetically advantageous at the low
prevailing levels of atmospheric oxygen prior to the Carboniferous period
(Ballantyne et al. 1987). However, it is notable that the relative concentrations of
the ions in sea-water and the body fluids of most vertebrates are still similar
(Epstein 1999). The utilization of urea as an osmolyte by the Chondrichthyes pre-
sumably was made possible following the acquisition of the ornithine-urea cycle.
Some osteichthyean fish, especially crossopterygians like the extant coelacanth,
probably also developed such an osmotic strategy based on the use of urea as an
osmolyte.
The fossil record identifies many freshwater, as well marine, species of ostra-
coderms in the Devonian. The transition to fresh water from the sea may have
occurred at the Silurian-Devonian boundary (Halstead 1985). It may have
involved an anadromous breeding migration by bony fish that were incipiently
euryhaline (Griffith 1987). Apart from an ability to excrete accumulated water,
such fish may have developed an ability to limit loss of, or even accumulate, salts
from across their gills. Extant freshwater fish can utilize branchial Na+ I H+ and
cl- I HC0 3- exchange mechanisms to take up sodium chloride. These exchange
processes are also present in marine hagfish, where they are utilized for main-

42
taining acid-base balance (Evans 1984). Thus, an ability to accumulate sodium
chloride across the gills could have been present in fishes before they entered fresh
water.
The transition of fish to tetrapod vertebrates and a terrestrial life appears to
have occurred in the Devonian and to have involved a crossopterygian (lobe-
finned) fish (order Rhipidistia) (Thompson 1980; Bray 1985). This momentous
evolutionary step to an amphibian could have been taken by a marine or fresh-
water species of fish. It could have been prompted by the drying up of a fresh-
water river or lake or the pollution of a coastal marine environment as a result
of flooding. A marine origin for the tetrapods is usually favoured by the pundits.
Such a fish, like the extant coelacanth, could have utilized urea as an osmolyte.
This strategy is also utilized by a contemporary estuarine amphibian, the crab-
eating frog. The presence of the ornithine-urea cycle and ureotelism would
appear to have been an essential prerequisite for a terrestrial life. (Uricotelism did
not, it seems, appear until much later.) Amphibians living on dry land have special
problems due to evaporation from their permeable skin. This limitation was
apparently not overcome until the evolution of the reptiles in the Carboniferous
period.
Cotylosaurian stem reptiles appear to have evolved from salamander-like
labyrinthodontian amphibians. Reptiles have been very successful in adapting to
dry terrestrial conditions. The stem cotylosaurians are thought, like extant turtles
and tortoises, to have been both ureotelic and uricotelic (Campbell et al. 1987).
(It will be recalled that some extant amphibians that live in dry exposed con-
ditions have also developed uricotelism.) Contemporary offspring of the
Lepidosauria, the lizards and snakes, and the Archosauria, the crocodiles and
birds, are uricotelic, which can result in a considerable reduction of their urinary
water loss. It seems likely that the dinosaurs, which were archosaurians, were also
uricotelic. Fish, amphibians and reptiles cannot form hyperosmotic urine and
in birds this ability is quite limited compared to that in mammals. Urates are
relatively insoluble and the danger of their precipitation in the renal tubule may
have limited such renal concentrating ability. However, the ability to excrete excess
salt as a hyperosmotic solution can have considerable benefits in water-saving.
Various secretory glands have been utilized for such salt excretion in reptiles and
birds. They have even been identified in fossil dinosaurs (Osmolska 1979;
Whybron 1981). However, they do not appear to have evolved in mammals, which
have, instead, a special capacity to form a hyperosmotic urine. This ability is
linked to the presence of the ornithine-urea cycle, which is necessary for the
establishment of high renal medullary tissue concentration gradients. They may
have acquired this ureotelism from the cotylosaurian reptiles.

43
Chapter 2

The Vertebrate Endocrine System

Osmoregulation is the process of physiological adjustment of the volume of water

and the concentrations of solutes in the cells and body fluids of organisms, in-
cluding the vertebrates. Such responses are usually necessitated by changes that
can occur as a result of the animal's interactions with its external environment
but also can be due to metabolic changes and disturbances, including disease.
Changes in the animal's fluid content and composition occur continually in poten-
tially hostile osmotic environments such as the sea, freshwater rivers and lakes,
and terrestrial habitats, which can even include hot dry deserts. Several types of
physiological responses may be involved in maintaining homeostasis of the body
fluids. They are mediated, depending on the species, by such organs and tissues
as the kidneys, urinary bladder, gut, salt -secreting glands, skin, gills and the blood
vascular system. The nature and duration of their physiological responses, coor-
dination with each other and the environmental events, necessitates the trans-
mission of chemical messages that are provided by neighbouring cells, nerves
and the endocrine glands. Osmoregulation can involve all of these coordinating
processes. However, the hormones secreted by the endocrine glands have special
roles that probably reflect their more persistent and ubiquitous effects.

1 Endocrine Function
Endocrine glands secrete hormones directly into the blood, which disseminates
them to distant organs and tissues. Such a release of hormones usually occurs in
response to specific stimuli. The glands may detect changes in the composition
and volume of the blood plasma or be stimulated to secrete by tropic hormones
and nerves. Hormones are widely distributed in the body but only certain tissues
and organs respond. Tissues identify hormones by the presence of "receptor"
molecules that can only bind and respond to specific hormones. Receptors may
be present in the cell membrane or the cytosol or be associated with genes in the
cell nucleus. Hormones have constitutive roles in regulating processes such as
growth and differentiation, reproduction, the metabolism of fats, proteins and
carbohydrates, and the volumes and composition of the body fluids. Hormones
can also contribute to rapid responses, such as may be precipitated by stressful
situations, when they usually act in conjunction with nerve impulses and local
hormones such as cytokines. Such physiological coordination occurs in all verte-
brates. However, it may differ somewhat, depending on the animal's natural envi-
ronmental circumstances and phylogeny. Thus, although all vertebrates possess

45
kidneys, only fish and larval amphibians have gills. The occurrence of salt glands
is phyletically sporadic and an ability to form hyperosmotic urine is present only
in birds and mammals. Morphologically homologous endocrine glands have been
identified in most of the main groups of vertebrates, but there are exceptions, such
as the lack of the parathyroid glands in fish. Hormones with similar, homologous,
chemical structures have a widespread distribution in vertebrates. However,
their precise structures may differ and even display evidence of an evolution. The
physiological roles of hormones may also display phyletic variation, and like
their structures, also have evolved. This area of study is known as comparative
endocrinology. Comprehensive reviews of this subject are available (Henderson
1997; Bentley 1998). There are many examples of such phyletic differences and
evolution in the processes of osmoregulation of vertebrates.

1.1 Overview

The principal endocrine glands, their secreted hormones and main functions
are shown in Table 2.1. It can be seen that their roles and functions encompass a
wide range of metabolic and physiological processes, and adaptive responses
to changes in the internal and external environments. They include the regula-
tion of the water and salt content of the body which, among various species, can
directly involve the actions of many different hormones. In tetrapod vertebrates
these include vasopressin (ADH), vasotocin, aldosterone, angiotensin II, adrena-
line, natriuretic peptides and the guanylins. Additional hormones with special
such roles in the fishes include growth hormone, IGF-I, prolactin, cortisol and,
possibly, the urotensins. Other hormones, such as adrenocorticotropin (ACTH)
and the hypothalamic hormones may be involved at a secondary, and even
tertiary, level, as they can influence the synthesis and release of more directly
involved hormones. Other hormones have indirect effects on osmoregulation,
such as those that mediate reproduction with its associated increased need for
water and salts. Thyroid hormone can increase the basal metabolic rate, and hence
evaporation, and its morphogenetic effects may contribute to the differentiation
of tissues, such as amphibian skin and fish gills, that influence osmoregulation.
Other endocrine glands are necessary for the sustenance of many tissues.
These hormones include insulin, glucagon, cortisol, leptin, parathyroid hor-
mone, calcitonin, 1,25-dihydroxyvitamin D3, adrenaline and angiotensin II. Hor-
mones clearly have multifacetted effects on living processes. The present account
is mainly concerned with those that have primary and secondary effects on
osmoregulation.

1.2 Architecture of Hormones and Receptors

Chemically, hormones may be peptides, (vasopressin and angiotensin), poly-

peptides, (ACTH and natriuretic peptides), proteins, (growth hormone and

46
Table 2.1. Summary of the principal endocrine glands in vertebrates: their secreted hormones
and main roles

Endocrine glands Principal hormones Main roles

Pituitary
Adenohypophysis ACTH, TSH, FSH, LH, GH, Tropic actions on endocrines
PRL Growth and differentiation
Neurohypophysis Vasopressin, vasotocin, Water metabolism, vascular
oxytocin-like peptides contractility Reproduction
Pars intermedia MSH Pigmentation (skin)
Hypothalamus CRH, TRH, Gn-RH, GH-RH Regulate hormones of
GH-R-IH, dopamine etc. adenohypophysis
Adrenal
Cortex Aldosterone, corticosterone, Na and K metabolism,
cortisol Intermediary metabolism
Medulla Adrenaline, noradrenaline "Stress" responses
Thyroid Triiodothyronine, thyroxine Basal energy metabolism
morphogenesis
Parafollicular "C" cells Calcitonin Calcium metabolism
(of thyroid)
(Ultimobranchial bodies)
Parathyroid glands Gonads Parathyroid hormone Calcium metabolism
Ovaries Estradiol-17~, progesterone Female reproductive system
Testes Testosterone, Sa- Male reproductive system
dihydrotestosterone
Islets of Langer hans Insulin (B-cells) Metabolism, proteins,
carbohydrates, fats
Glucagon (A-cells) As above, generally opposes
insulin
Pineal Melatonin Biological rhythms,
especially reproduction
Liver Angiotensinogen Adrenal cortex, thirst, blood
(prohormone), pressure
Angiotensin II
IGF-I (induced by GH) Growth, differentiation
Kidney Renin Angiotensin I from
angiotensinogen
Heart Natriuretic peptides Regulation extracellular
volume
Adipose tissue Leptin Appetite regulation,
proreproductive
Skin Vitamin D3 (prohormone) Calcium metabolism
Gastrointestinal tract Gastrin, cholecystokinin Digestion, absorption, feeding
secretin, guanylins etc.
Corpuscles of Stannius Stanniocalcin Calcium metabolism
(some fish)
Urophysis (some fish) Urotensin I and II Possible roles in
osmoregulation

47
prolactin), amino acid derivatives (adrenaline and thyroid hormone) and steroids
(aldosterone and cortisol). Some hormones, such as the amino acid derivatives,
are quite small molecules, but the proteins can have a molecular mass over
30 kDa. Receptors for hormones are large proteins and glycoproteins. The chem-
ical structures of hormones and receptors are prescribed by the animal's genes.
The structures of hormones and receptors determine their abilities to interact
with each other and initiate a specific response. For a hormone this configuration
is called its structure-activity relationship (SAR). In nature, and as a result of
the manipulations in the chemist's laboratory, hormones may display variations
(polymorphism), especially in different species of animals. Structural variants
of a particular hormone may also exist in a single species or even an indivi-
dual animal. Receptors also display such structural variability. Variations in the
structures of a particular hormone and its receptors may have little effect on
the qualitative nature of the response, though quantitative differences may result.
However, more critical changes in structure can precipitate in the abolition of an
ability to initiate a particular response and even presage the evolution of a novel
hormone. Chemically homologous hormones and receptors can often be classi-
fied into families and superfamilies, the individual members of which may,
nevertheless, mediate quite different types of responses. At least 14 different pep-
tides that are related to mammalian vasopressin have been identified in different
species of vertebrates. Most animals have at least two of them, which can react
with at least two different types of receptors and initiate a wide variety of effects.
The responses, in different species, include increases in the water permeability of
kidney tubules and amphibian skin and urinary bladder, a contraction of blood
vessels, a release of ACTH, contraction of the uterus or oviduct, and the release
of milk from mammary glands.
Different parts of hormones and receptors contribute to various aspects of
their functioning. In polypeptides and proteins these regions are often des-
cribed as domains which contain specific sequences of amino acids. Recognition
and binding domains are concerned with the interactions between hormones
and their receptors. Receptors may also have transmembrane domains, which
anchor them in the cell membrane, dimerization domains, which are involved in
their abilities to associate with each other, and transactivation domains, which
are concerned with initiation of the response. The structures of hormones can
also incorporate other properties such as may contribute to their abilities to
bind to plasma proteins and their metabolic destruction and clearance from the
blood.

1.3 Morphology of the Endocrine Glands

The endocrine glands usually occupy comparable positions in the bodies of all
vertebrates and exhibit characteristic morphological structures. They generally
have a plentiful blood supply into which they directly secrete one or more
hormones. A nerve supply may contribute to such a release of hormones and

48
regulate the blood flow. There are some phyletic differences in the occurrence of
the endocrine glands. Parathyroid glands are not present in fish. Hagfish, croco-
diles and whales lack a pineal gland. Some fish possess special endocrine glands,
for instance the corpuscles of Stannius and the urophysis, which are absent
in tetrapods. The various cells that aggregate to form endocrine glands may
have quite different embryonic origins. Thus, the neurohypophysis and adrenal
medullary tissue are derived from neural tissue, the adenohypophysis from ecto-
derm and the adrenal cortex from mesoderm. Endocrine glands may be divided
into distinct lobes, as seen in the pituitary, a cortex and medulla, as in the mam-
malian adrenal, and the zones of the adenohypophysis and mammalian adrenal
cortex. Such morphological divisions are usually related to the synthesis and
secretion of different hormones. Not all endocrine cells aggregate into distinct
glands. There are, for instance, many types of hormone-secreting cells that are
individually dispersed in the mucosal lining of the gut. Various tissues and vis-
ceral organs may also function as endocrine glands and secrete hormones. The
heart secretes natriuretic peptides, fat cells produce leptin, the liver IGF-I and
angiotensinogen and the kidney renin and 1,25-dihydroxyvitamin D3 • On specific
occasions, a variety of other tissues can secrete hormones, including the placenta,
mammary glands and some tumours.

1.4 Synthesis of Hormones

Endocrine cells sometimes synthesize hormones in situ from either amino acids
or cholesterol. This process often occurs in response to, and with the aid of tropic
hormones from other endocrine glands. Examples include the actions of ACTH
and angiotensin II on the adrenal cortex, thyrotropin on the thyroid gland and
gonadotropins on the gonads. Some hormones are stored following their syn-
thesis in granules, vesicles and tissue follicles. Others, especially the steroidal
hormones, are promptly released into the circulation. The chemical design of hor-
mones and their biosynthesis are directed by their genes. Peptide, polypeptide
and protein hormones are made from precursor proteins (preprohormones and
prehormones) that are produced by genetic transcription and translation. On the
other hand, adrenaline and thyroid hormones are made from tyrosine, melatonin
from tryptophan and steroid hormones from cholesterol. The chemical substitu-
tions involved in the conversions of these substrates to the hormones are the
results of sequences of chemical reactions that are controlled by enzymes. They
usually occur in the endocrine cell, but an "activation" of a hormone may some-
times occur in peripheral tissues.
Following their formation on the ribosomes, preprohormones and prehor-
mones are directed by the N-terminal signal sequence of amino acids to the endo-
plasmic reticulum (ER). This signal peptide is then removed, which results in the
formation of a prohormone or a hormone. The latter occurs in the synthesis of
growth hormone and prolactin. A prohormone or newly formed hormone may
undergo further posttranslational processing in the cisternae of the ER, where

49
molecular folding, cross-linking, acetylation and glycosylation can occur. On
passing to the Golgi apparatus, the prohormone may undergo selective cleavages
of its amino acid sequence to produce a single or even several hormones. Multi-
ple copies of a single hormone or several different hormones may be produced
in this way from a single prohormone molecule. Thus, the prohormone proopi-
omelanocortin (POMC), which is produced by the pituitary, can provide ACTH,
a-MSH, ~-MSH and several other biologically active molecules, including Met-
enkephalin and ~-endorphin. Such cleavage of the prohormone occurs at prede-
termined sites in the molecule, usually involving basic arginine and lysine
residues. This process results from the actions of enzymes called subtilisin-related
convertases (SPCs). The posttranslational processing of prohormones may vary
in different endocrine glands. Thus, ACTH and ~-endorphin may be produced
from POMC in the adenohypophysis and a- and ~-MSH, and ~-endorphin in the
pars inter media. (A single gene may also give rise to different hormones as a result
of differences in posttranscriptional processing, alternate-splicing, of its precur-
sor RNA.)
The synthesis of steroid hormones from cholesterol involves the actions of
a succession of enzymes that are associated with the ER and mitochondria in
steroidogenic cells. The early steps in this synthesis are shared by the adreno-
cortical and gonadal steroid hormones. However, the subsequent biosynthetic
changes are more specific. Thus, aromatization enzymes produce oestrogens
from androgen substrates, 11~-hydroxylase produces corticosterone from 11-
deoxycorticosterone and cortisol from 11-deoxycortisol, and aldosterone syn-
thetase converts corticosterone to aldosterone.

1.5 Release of Hormones

A release of hormones from an endocrine gland into the blood may occur in
response to stimuli which signal a physiological imbalance, changes in environ-
mental conditions, pending events, such as reproduction and migration, and
physical and emotional stress. Such hormone release may be constitutive, and
occur continuously, sporadically, such as in response to an acute need, or rhyth-
mically. Hormones may be released in small pulsatile bursts or tonically in
a steady stream. Rhythmical release may be related to regular events, such as
day and night, the seasons and the activities of endogenous biological clocks. A
variety of receptor mechanisms may be involved in triggering the release of
a hormone. Endocrine cells may respond directly to concentrations of ions, nu-
trients and the osmotic and hydrostatic pressures of its perfusing blood. Recep-
tors for tropic hormones may be present in the cell membrane. Responses of
endocrine glands to neural stimuli may be mediated by receptors and ion chan-
nels. Hormones are secreted from endocrine cells by diffusion or exocytosis fol-
lowing the fusion of storage granules and vesicles with the cell membrane. Such
an event may be linked to electrical depolarization or transduced by elevations
of cell Ca2+ concentrations and the activities of the adenylate cyclase-cAMP and
phospholipase C-phosphatidylinositol signalling systems (see later).

50
1.6 Hormones in the Blood

Physiologically effective concentrations of hormones in the blood plasma range

from about 10-7 to 10- 11 M. They may be in aqueous solution or bound to plasma
proteins. The lipid-soluble steroid hormones and thyroid hormone can achieve
higher concentrations by such binding. The transport of hormones to their effec-
tor target sites will also be facilitated. Other hormones, including growth
hormone, prolactin and IGF I, may also be bound to proteins in the plasma. For
a response to occur, the hormones must enter the aqueous phase and be "free" in
solution so that they can combine with their receptors. In some instances, as much
as 99% of a hormone may be bound while only 1% is free in solution. However,
this proportion varies with the different hormones. Some hormones may bind
to plasma albumin in a relatively non-specific manner (low-affinity binding)
though in relatively large amounts (high capacity). However, some proteins may
be present in the plasma, at lower concentrations, which can bind hormones
more specifically (high-affinity but low-capacity). They include corticosteroid-
binding globulin, (CBG), which binds 80 to 90% of the cortisol and corticosterone
that is present in the plasma, though only 20% of the aldosterone. The binding
of hormones to proteins in the plasma can have a number of consequences on
their actions, apart from facilitating their transport. They may also protect tissues
from possible toxic effects of high aqueous concentrations of a hormone. Binding
of hormones may impede or facilitate the transport of a hormone across barri-
ers in capillary beds, such as those in the kidneys and brain. The clearance of a
hormone from the plasma may also be reduced so that its action will be more
prolonged.

1.7 Peripheral Metabolism of Hormones

Hormones, following their release into the blood, undergo metabolic changes
which can either increase (activation) or decrease their effectiveness. Such
processes occur in peripheral tissues, especially the liver and kidneys, and also
their target organs. These chemical changes include the cleavage of polypeptides
and proteins by peptidase enzymes. The enzymes may act at internal sites or
the amino- or carboxy-terminals of such molecules. They are then called, respec-
tively, endopeptidases and amino- or carboxy-peptidases. The initial formation,
activation and final demise of the octapeptide hormone angiotensin II involves
the actions of all such types of these enzymes. Hormones can be inactivated by a
reduction of cross-linking disulphide bonds. Oxidation reactions, such as the con-
version of hydroxyl to keto groups, are often involved in the inactivation of steroid
hormones. Conversely, a reduction of a keto to a hydroxyl group can occur and
can, for instance, activate cortisone, to form cortisol. Vitamin D3 is activated to
1,25-dihydroxyvitamin D3 by two successive hydroxylations, which occur first
in the liver and then the kidney. The inactivation of adrenaline involves the
processes of methylation of its aromatic ring and the deamination of its side
chain. Thyroxine (T4 ) contains four atoms of iodine. Removal of one of these, at

51
the 51 position, results in the formation of triiodothyronine (T 3), which is much
more active. Further such deiodination, by deiodinase enzymes, however, results
in its inactivation. Steroid and thyroid hormones can undergo conjugation reac-
tions to form glucuronide and sulphate compounds. This process abolishes their
biological activity and also increases their water solubility so that they can be
excreted more readily in the urine and bile.

1.8 Mechanisms of Hormone Action

Osmoregulatory responses to hormones involve such processes as the absorption

and secretion of water and electrolytes, especially Na+, K+ and cl-, across epithe-
lial membranes in the kidneys, gut, urinary bladder, gills, skin and salt glands.
The structure and metabolic integrity of such tissues and organs can be modu-
lated by hormones. Such processes include cell growth and differentiation, and
the functioning and replication of their transporter proteins. The cardiovascular
system can influence osmoregulation. It not only provides sustenance but also
mediates the exchanges of fluids between the plasma and the intercellular com-
partment, and the formation of the glomerular filtrate by the kidneys. Hormones
can have special roles in regulating such processes by influencing the contractil-
ity of vascular smooth muscle in small blood vessels. The effects of a hormone
commence with its binding to its receptors and conclude with the response of
its target tissue. The molecular processes that link these events are called signal
transduction (Hunter 2000). It involves a translation and amplification of the
hormone's message to induce a morphological or physiological change in the
effector. The mechanism usually involves a complex cascade of biochemical
events in the cell. An activation of a variety of proteins, especially enzymes, usu-
ally takes place. The latter include many protein kinases (Hunter 2000), which, by
utilizing ATP as a substrate, can phosphorylate tyrosine, serine and threonine
residues on proteins and so change their inherent activities. Such events usually
involve the induction of conformational changes. These proteins may be other
enzymes, transcription factors and structural components of cells.
Receptors for hormones, as described earlier, may be present in the cell mem-
brane or the cytoplasm, or be associated with the nucleus of the cell. They are
proteins or glycoproteins, which include a number of functional domains. Such
sequences of amino acids are involved with ligand (hormone) binding (the recog-
nition site), anchorage in the cell membrane (transmembrane domain), binding
to a nuclear-response element and the formation of receptor dimers. Membrane-
associated receptors are elongated molecules which lie in the plasma membrane.
Their N-terminus projects into the extracellular fluid and their C-terminus
into the cytoplasm. The recognition site of these receptors is usually associated
with the extracellular portion of the molecule or, sometimes, the transmembrane
domain. The cytoplasmic portion of the receptor often, but not always, has
enzymatic activity and contains a catalytic site. The membrane receptor may cross
the cell membrane once or recross its several times in a serpentine-like manner.
Such receptors have a capacity to move laterally and some may then associate

52
with others to form dimers. Such combinations may be necessary for their func-
tioning. Similarities in the structures of receptors often allow them to be classi-
fied into families and superfamilies which appear to reflect a common primeval
ancestry.
The binding of a hormone to its receptor is thought to result in a conforma-
tional change in its structure, which provides the initiating transduction signal.
It may result in the formation of a dimer with a neighbouring receptor of the
same, or even different ilk, the dissociation of a contained inhibitory component,
migration to the cell nucleus or the activation of an endogenous enzymatic activ-
ity. Such events constitute the first period of the transduction process.

G-Protein-Linked Receptor Mechanisms. Many m·embrane receptors are asso-

ciated with heterotrimeric G-proteins that transduce the response to juxtaposed
enzymes, such as adenylate cyclase and phospholipase C. The activity of G-
proteins is influenced by their binding to the guanosine nucleotides GDP and
GTP. Hormone receptors which utilize this mechanism include vasopressin,
adrenaline, ACTH and angiotensin II. The transmembrane domains of these
receptors characteristically cross and recross the cell membrane seven times.

The Actions of Vasopressin V2 Receptors, Adrenaline ~-Receptors and ACTH

Receptors. These are linked to adenylate cyclase in the cell membrane (Fig. 2.1).

Receptors IS'-r'l [\Jil

(G.}_ _@_ Plasma membrane
.----'~o....;;.c.--il AC J ~
GTP GD~ ~ GDP GTP
a.-GTP ~ ai-GTP
CyclicAMP ATP Phosphodiesterase S'AMP
Activates!
CyclicAMP •

-0~0KA Protein-serine-P04 Biological

Protein-serine-OH i- Protein-threonine-P04 ~ respon~s
Protein-threonine-OH .____. { Phosphoprotem
ATP ~ ADP Protein-serine-OH ~phosphatase
Cytoplasm Phosphorylation Protein-threonine-OH Pi

Fig. 2.1. A diagramatic summary of the mechanism of action of hormones, such as vasopressin
and vasotocin (V, type receptors) and adrenaline (~-adrenergic receptors), that utilize the
adenylate cyclase-cyclic AMP and G protein systems. AC Adenylate cyclase; G, and G; G proteins
with stimulatory (S) and inhibitory (I) effects; a ; and a, activated inhibitory and stimulatory
subunits, respectively, of G proteins; H hormone; I inhibition; PKA Proteinkinase A; C catalytic
unit of PKA; R regulatory subunit of PKA; S stimulation. For further information see the text.
(Bentley 1998)

53
The G-proteins consist of a, ~ and y subunits. The a-subunit bind is bound to
GDP. Following the activation of the receptor by the hormone, the GDP on this
subunit is replaced by GTP. A dissociation of a-GTP subunit from the G-protein
then follows and results in an activation of adenylate cyclase. The a-GTP pos-
sesses intrinsic GTPase activity and quickly reverts to a-GDP, which then recom-
bines with the ~-y subunit. The a subunit can exist in two forms, a, which
stimulates adenylate cyclase activity, and the other, a" which inhibits it.
The activated adenylate cyclase forms cAMP from ATP. This nucleotide, which
is called a second messenger (the hormone being the first messenger), combines
with the regulatory subunit of serine I threonine protein kinase A (PKA),
releasing its active catalytic unit. The PKA can phosphorylate a variety of
proteins that are involved in the response of the effector. Such proteins include
the transcription factor CREB that binds to cAMP-response elements (CRE) in
the cell nucleus.
G-proteins also link hormonal responses that involve the activation of phos-
pholipase C (PLC) (Fig. 2.2). This membrane enzyme is linked to a 1-adrenergic
receptors, V 1• vasopressin receptors and angiotensin AT 1 receptors. The G-protein
subunit involved is aq. The membrane lipid phosphatidylinositol 4,5-bisphos-
phate (PIP 2) is its substrate. Two second messengers result: diacylglycerol (DAG)
and inositol-1,4,5-trisphosphate (IP3). The DAG activates protein kinase C (PKC)
while IP 3 mobilizes Ca2+ from the endoplasmic reticulum. The Ca2+ can combine

Plasma membrane

Fig. 2.2. A diagramatic summary of the mechanism of action of hormones, such as vasopressin
and vasotocin (V2-type receptors), angiotensin II and adrenaline (a-adrenergic receptors) that
utilize the phospholipase C-phospatidylinositol system. DAG Diacylglycerol; ER endoplasmic
reticulum; G protein Gq; H hormone; IP3 inositol-1,4,5-trisphosphate; PLC phospholipase C;
R receptor. For further information see the text. (Bentley 1998)

54
with the intracellular protein calmodulin and initiate various responses, includ-
ing activation of protein kinases and phosphodiesterase. The latter inactivates
cAMP.

The Insulin Receptor Protein Tyrosine Kinase-MAP Kinase Pathway. The

insulin receptor superfamily includes membrane receptors for IGF-I, which
mediate many effects of growth hormone, including the adaptation of some
teleost fish to life in the sea. Insulin and IGF-I have also been observed (in vitro)
to increase Na+transport across some epithelial membranes, such as the amphib-
ian urinary bladder and skin (Blazer-Yost et al.1989). Insulin and IGF-I receptors
have a homology in their amino acid sequences of about 50% (Prager and Melmed
1993). A homologous insulin-IGF-I type receptor has been described in a proto-
chordate (amphioxus, Branchiostoma) (Chan et al. 1992). Such receptors mediate
the various effects of such hormones on metabolic processes and cell division,
growth and differentiation. They typically consist of two pairs of subunits, a and
p, that are linked by disulphide bonds (Kahn et al. 1993). The a subunit projects
into the extracellular fluid and contains the hormone-binding site while the P
subunit has a cytoplasmic domain that possesses intrinsic tyrosine kinase activ-
ity. The binding to the hormone results in a lateral movement of the receptors.
They then form dimers, which results in conformational changes and the activa-
tion, by autophosphorylation, of the cytosolic tyrosine kinase domain of the
receptor (Saltiel 1996; Schlessinger 2000). This event initiates the activation of a
cascade of kinase enzymes. This process is initiated by the activation of a small
G-protein called Ras that is associated with the cell membrane. It is linked to the
receptor tyrosine kinase by an adaptor protein (Grb 2 ) and a guanylate nucleotide
exchange factor (GEF or SOS protein). The phosphorylation kinase cascade can
result in the activation of MAP-kinases (mitogen-activated proteins), which can
enter the nucleus and activate transcription factors. The activated tyrosine kinase
may also contribute to the functioning of other intracellular processes.

The Janus Kinase-STATS Pathway. This mediates the actions of growth

hormone and prolactin. Growth hormone and prolactin contribute to the
osmoregulatory adaptations of some fish during their migrations between rivers
and the sea. The receptors for these hormones span the cell membrane but do not
appear to possess any intrinsic enzymatic activity. They belong to the cytokine
receptor superfamily that also includes receptors for several cytokines such as
erythropoietin and interferons (Bazan 1990; Nakagawa et al. 1994). Such recep-
tors have been identified in osmoregulatory tissues of teleosts (Sandra et al. 2000).
They mediate processes including cell growth, development, locomotion and
repair. Responses to these receptors are transduced by cytosolic tyrosine kinase
pathways, which results in the activation of transcription factors (Finidori and
Kelly 1995; Carter-Suet al. 1996; Horseman 1997). The receptors form dimers fol-
lowing their binding to the hormones. This event signals their cytosolic domains,
which then each combine with a molecule of Janus kinase (JAK). A number of
types of these tyrosine kinases exist (JAKI> JAK 2 etc.) in the cytoplasm. When they
are associated with the receptor they can phosphorylate and activate trans-
cription factors called STATs (signal transducer and activator of transcription).

55
Following such activation, STATs form homo- and hetero-dimers and enter the
cell nucleus, where they can initiate transcription. One of the proteins induced in
the liver by growth hormone is IGF-1, which, as described above, contributes to
the adaptation of some teleost fish to life in sea-water.

Membrane Guanylate Cyclase and the Receptors for Natriuretic Peptides and
Guanylins. Guanylate cyclase hydrolyzes GTP to cGMP, which, like cAMP, can act
as a second messenger and activate protein kinases. Guanylate cyclase exists in a
soluble form in the cytoplasm, where it may be involved in such processes as neu-
rotransmission and the relaxation of vascular smooth muscle. This form of
guanylate cyclase can be activated by nitric oxide (NO), which is formed from
arginine by nitric oxide synthase (NOS). A second form of guanylate cyclase is
associated with the cell membrane, where it can be an integral part of receptors
for the natriuretic peptides and guanylins. These peptides promote the secre-
tion of sodium chloride by the kidney and, in the instance of the guanylins,
also the intestine (Atlas and Maack 1992; Forte et al. 2000). The natriuretic peptide
hormone receptors (GC-A, GC-B and GC-C) have a single transmembrane
domain linking an extracellular ligand-binding domain with a cytosolic domain.
The latter possesses intrinsic guanylate cyclase activity (Chinkers et al. 1989).
Transmembrane signalling, as a result of ligand binding, results in the activation
of this enzyme and the formation of cGMP. This nucleotide can activate protein
kinases including cGMP-activated protein kinase II and it can also activate cAMP-
dependent protein kinase. The CFTR chloride channels in intestinal mucosal cells
can be activated as a result of phosphorylation by these kinases (Forte et al. 1992;
Vaandrager et al. 1997). It has also been shown that cGMP can inhibit the activi-
ties of sodium channels (ENaC) in the kidney collecting ducts (Light et al. 1989).
Apart from phosphorylation of proteins, cGMP may have more direct effects on
ion channels such as by binding to components that modulate their gating mech-
anisms. (Finn et al. 1996).

Steroid Hormone-Activated Transcription Factors. The receptors for steroid

hormones and thyroid hormone have many structural similarities and are con-
sidered to belong to the same protein superfamily. They are principally present
in the region of the cell nucleus where they can bind to DNA. These receptors are
actually transcription factors that can be activated by directly binding to hor-
mones. Steroid hormones are lipophilic and so can cross the cell membrane
by diffusion (Fig. 2.3). Some may interact with receptors in the cytoplasm,
but more usually this interaction occurs in the nucleus. The steroid hormones
contribute to many homeostatic mechanisms. The regulation of sodium and
potassium metabolism is the province of the adrenocorticosteroids, especially
aldosterone, but in teleost fish cortisol is involved. Their receptors contain
domains with special functions. A hormone-binding domain is present at the C-
terminus and a transactivation domain, which stimulates transcription, at the
N-terminus. A DNA-binding domain and dimerization domain lie in the middle
of the receptor. The amino acid sequences of such domains vary for the different
steroid hormones and species, but they still display considerable homologies. The
DNA-binding domain of the human glucocorticoid receptor has a 97% homology

56
 u
Plasma membrane
Receptor binding?

®- • ®
r~
mRNA

D•
Pre-mRNA Splicing!
Transcription Promotor

Receptor~
I GENEX (DNA)
l[j
®- ® -...:. TA HB o •
(H) (I!)
E]+-~
,....--

!Nucleus ~T
Dimerization-
Biological
response Ill I\IMNVV1 ~Ri~som5s
Cytoplasm Protein X ~ Translation

Fig. 2.3. A diagramatic summary of the mechanism of actions of steroid hormones, such as
aldosterone, that utilize the process of genomic transcription. DNA-B DNA-binding domain;
H hormone; HB hormone-binding domain; HRE hormone-response element; IP inhibitory
protein; TA transcriptional activation domain. For further information see the text. (Bentley
1998)

in its amino acid sequence to that in the rainbow trout (Ducouret et al.1995). The
hormone-binding domains of these hormones have a 70% homology. The effects
on sodium and potassium metabolism are usually mediated by mineralocorticoid
receptors (MR) and those on protein, fat and carbohydrate metabolism by gluco-
corticoid receptors (GR). However, teleost fish have only one adrenocorticosteroid
hormone receptor that mediates both types of effects and its structure is GR-like.
Interactions of the steroid hormone receptors with hormones result in a struc-
tural change, which includes the unmasking of a site that facilitates the formation
of a homodimer. (Some steroid hormones receptors form heterodimers.) The
activated hormone receptor-transcription factor moves to the gene and combines
with a specific DNA sequence, called the hormone-response element (HRE), on
the promoter. (An enhancer DNA sequence, which can increase utilization of the
promoter, is sometimes activated.) A multiprotein transcription initiation com-
plex is assembled on the promoter and guides the actions of RNA polymerase II
at the initiation site. The transcription of RNA follows, resulting in the formation
of specific proteins that mediate the response. In the instance of mineralocorti-
coids, such proteins can include Na-K-ATPase and sodium channels (ENaC).

2 Osmoregulatory Hormones

A variety of hormones secreted by endocrine glands directly contribute to the

regulation of the accumulation, conservation and excretion of water and salts in
the body; Table 2.2). Others indirectly influence such processes as a consequence

57
V1
00

Table 2.2. Hormones that contribute to osmoregulation in vertebrates

Hormone Site of origin Chemical nature Osmoregulatory target organs Principal effects

Primary effects
Vasopressin (antidiuretic Neurohypophysis Nonapeptides Kidney, blood vessels, Antidiuresis. In amphibians water
hormone, ADH), amphibian skin and bladder uptake across skin and bladder.
vasotocin (AVT) Vasoconstriction
Natriuretic peptides Heart, also brain Polypeptides Kidney, adrenal cortex, blood Regulate extracellular fluid volume;
(ANP, BNP, CNP etc.) vessels, gills natriuresis, diuresis, vasodilatation,
Inhibit synthesis of aldosterone
Angiotensin II (from Renin-angiotensin Octapeptide Kidney, adrenal cortex, blood Increases corticosteroids, drinking,
angiotensinogen) system (kidney, vessels, hypothalamic Na-appetite. Vasoconstriction
plasma) thirst -centre
Growth hormone Adenohypophysis Protein Gills of teleost fish (Cl-cells) Induces IGF-I, increased ability to
extrude cl-
Prolactin Adenohypophysis Protein Gills of teleost fish (Cl-cells). Decreases salt loss from gills
Also gut, bladder, kidney? during adaptation to fresh water.
Decreased permeability to water
Aldosterone Adrenocortical tissue Steroid Kidney, colon, sweat glands, Na+ retention and absorption, K+
amphibian skin and bladder, secretion
reptile salt glands
Cortisol Adrenocortical tissue Steroid Gills of teleost fish (Cl-cells) Promotes salt secretion in sea-water
Also gut and (?) kidneys. Salt uptake in fresh
Adrenaline and Chromaffin tissue, Catecholamines Cardiovascular system, Vasoconstriction, vasodilatation,
noradrenaline adrenal medulla (amino acid epithelial permeability, altered ion transport and
derivatives) (kidneys, gills, amphibian permeability to water
.skin).
Guanylins Intestine Pep tides Kidney and gut epithelia Promotes Cl- secretion
 Se~ondary and Tertiary Effects
Adrenocorticotropin Adenohypophysis Polypeptide Adrenocortical tissue Increases synthesis of cortisol,
(ACTH) corticosterone and can facilitate
that of aldosterone
Corticotropin-releasing Hypothalamus Polypeptide Adenohypophysis Increases release of ACTH
hormone (CRH)
Dopamine Hypothalamus Catecholamine Adenohypophysis Inhibits prolactin release
Growth hormone-R-H Hypothalamus Polypeptide Adenohypophysis Increases release of growth hormone
Somatostatin Hypothalamus etc. Peptide Adenohypophysis Inhibits release of growth hormone

Indirect Effects on Use of Water and Salt

Oestrogens, androgens Gonads Steroids Reproductive organs Supports reproductive cycles, care of
and progesterone (primary and secondary) young, migration
Gonadotropins (LH, FSH) Adenohypophysis Glycoproteins Gonads Control reproductive cycles
Thyroid hormone Thyroid gland Iodinated amino Most tissues Morphogenesis (includes amphibians
(triiodothyronine, T3 ) acid derivative and fish), increased metabolic rate
in homeotherms

General tissue support

Insulin, glucagon Islets of Langerhans Protein, polypeptide Liver, muscle, fat cells Regulate metabolism of proteins, fats,
Cortisol, growth hormone see above and carbohydrates
Parathyroid hormone Parathyroid gland Polypeptide Kidney, gut, bone, gills Regulate calcium metabolism
Calcitonin Thyroid "C" cells Polypeptide
Stanniocalcin Corpuscles of Stannius Polypeptide
Vitamin D3 Skin and diet Sterol

U1
\0
of their tropic actions on these glands and effects on the morphological and
metabolic integrity of the target organs involved. The particular hormones in-
volved in the osmoregulation of vertebrates often display differences in their
chemical nature, physiological effects and the particular target organs and tissues
where they act. The following is a comparative description of such hormones
in the vertebrates. General references are Henderson (1997) and Bentley (1998).
Summaries are provided in Tables 2.1 and 2.2.

2.1 The Hypothalamus and Pituitary Gland

The hypothalamus and pituitary gland function as an integrated neuroendocrine

complex that is the major interface between the nervous and endocrine systems.
It makes important contributions to osmoregulation (Denton et al. 1996) and
many other activities of the endocrine glands. Both tissues secrete hormones
and lie adjacent to each other at the base of the forebrain (diencephalon) below
the third ventricle. The hypothalamus is formed embryonically as a thickening
of the floor and side of the third ventricle and runs from the optic chiasma
caudally to the midbrain. The pituitary lies beneath it. They communicate by
means of both neural connections and a system of blood vessels, the hypophysial-
pituitary portal system, that originates in the median eminence regions of the
hypothalamus.
The hypothalamus (see Fig. 2.4) is the site of complex neural networks in which
the cell bodies form a number of aggregates called nuclei. The larger, magnocel-

Brain

Paraventricular
Para tuberalis
nucleus
Supraopticohypophysial
tract

Pars intermedia

Pars nervosa
(neurohypophysis)

Adenohypophysis ~ars tuberali/ Secondary

(anterior lobe) capillary network
Pars dislalis

Fig. 2.4. A diagrammatic depiction of the amniote pituitary gland and the associated region of
the hypothalamus. In anamniotes the neurohypophysis does not form a distinct neural lobe. In
teleost fish the interactions o f the hypothalamus and adenophypophysis are principally due to
neural rather than v ascular connections. For further details see the text

60
lular, neurons form the supraoptic nuclei (SON) or, in fishes and amphibians, the
preoptic nucleus. These neurons have neurosecretory activity and are the sites
of formation of the neurohypophysial peptide hormones. Smaller, parvicellular,
neurons also form such nuclei, including the arcuate and paraventricular nuclei
(PVN) which secrete several "releasing" hormones into the portal blood vessels.
These hypothalamic hormones travel to the anterior lobe of the pituitary gland
(the adenohypophysis or pars distalis), where they can regulate the release of its
hormones. The hypothalamus has many other functions that are mostly con-
cerned with integrating and maintaining bodily homeostasis. It contributes to
the regulation of the cardiovascular system, body temperature, feeding, thirst
and salt appetite. Neurons in the hypothalamus can also detect the levels of
steroid hormones in the peripheral circulation and so provide feedback signals
that can control the release of ACTH as well as gonadotropins. Thus, the
hypothalamus has several important roles that are related to the animal's
osmoregulation.
The pituitary gland (hypophysis) secretes at least nine different hormones, four
of which have important effects on osmoregulation in various species. Embryon-
ically, the pituitary has a dual origin, being formed by a downgrowth of neural
tissue from the brain and an upgrowth of ectodermal tissue from the roof of the
pharynx. The former (Fig. 2.4) becomes the neurohypophysis (pars nervosa) and
the latter the adenohypophysis, which includes the pars distalis, pars tuberalis and
pars intermedia. The pars distalis and pars tuberalis are sometimes called the
anterior lobe of the pituitary, the pars nervosa the posterior lobe and the pars
intermedia the intermediate lobe. The neurohypophysis retains neural con-
nections to the hypothalamus through the infundibular stalk, which carries the
nerve fibres of the supraopticohypophysial tract. The hormones secreted by
the neurohypophysis, in mammals vasopressin and oxytocin, are formed in the
cell bodies of the SON and PVN and travel down their axons to the pituitary. The
adenohypophysial hormones are synthesized in specialized cells including
the corticotropes (ACTH), gonadotropes (FSH and LH), thyrotropes (TSH) and
somatomammotropes (GH and prolactin).
The general pattern of the morphology of the pituitary and hypothalamus is
similar throughout the vertebrates, but some differences occur. The neurohy-
pophysis is enlarged in tetrapods, as compared to the fishes, and is called the
neural lobe. This change has been associated with a terrestrial manner of life and
a greater quantity of stored hormones. A hypophysial-pituitary portal blood sys-
tem is absent or poorly developed in teleost fish. Instead, they utilize neural con-
nections between the two tissues. Hagfish and lampreys (Agnatha) lack both
vascular and neural connections between the hypothalamus and pituitary. The
hypothalamic hormones apparently depend on diffusion to gain access to the
pituitary. Birds lack a pars intermedia and it is poorly developed in some mam-
mals, including humans, elephants and whales.

Neurohormones of the Hypothalamus. At least six different hormones have

been identified in the hypothalamus. However, it is suspected that several others,
often referred to as factors, may exist. Usually, such a hormone or factor has been
found to either increase or inhibit the release of a specific pituitary hormone.

61
[Thus, in naming such excitants the suffixes -RH (releasing) and -IH (inhibiting)
are often used.] However, in some instances, it is suspected that a single such
hypothalamic hormone can influence the release of more than one pituitary
hormone. For instance: thyrotropin-releasing hormone (TRH) may sometimes
also promote the release of growth hormone and prolactin. The release of some
pituitary hormones is under dual control of hypothalamic hormones, one of
which increases while the other decreases, release. All of the identified hypo-
thalamic hormones are peptides or polypeptides with the single exception of
dopamine (which is a catecholamine). Dopamine functions as a prolactin release-
inhibiting hormone (P-R-IH). Growth hormone (GH) is under the dual control of
GH-RH (a polypeptide containing 37 to 45 amino acid residues) and somatostatin
(GH-R-IH containing 14 amino acids). The release of ACTH (corticotropin) is
promoted by CRH (contains 41 amino acids) and is possibly inhibited by CRIF
(Redei et al. 1995). Vasopressin is better known as a neurohypophysial hormone
with an antidiuretic action, but it can also promote the release of ACTH. This
response may occur under conditions where stress is a predominant stimulus for
the release. Hypothalamic hormones have been identified throughout the verte-
brates, but their amino acid sequences usually display differences that can be
related to their phylogeny. Several of them also occur at other sites in the body
such as the brain. Somatostatin can also contribute to the control of secretion of
insulin and gastric juices. Corticotropin-releasing hormone is also expressed in
the mammalian placenta and appears in the peripheral circulation. It may be
involved in the initiation of parturition (Challis and Lye 1994).

The Peptide Hormones of the Neurohypophysis. Most vertebrates can secrete

two structurally related hormones from the neurohypophysis (Fig. 2.5). In
mammals they are vasopressin (ADH) and oxytocin. Other phyletic groups of
vertebrates usually secrete vasotocin and an oxytocin-like peptide. Vasopressin
and vasotocin regulate the excretion of water by the kidneys of tetrapods and
therefore play an important role in their osmoregulation. In mammals, oxytocin
contributes to the reproductive process by its ability to contract the uterus during
parturition and to promote the let down of milk by the mammary glands.
The role of oxytocin-like peptides in non-mammalian vertebrates is uncertain.
However, about 14 such peptides have been identified in species ranging from
mammals to fish. Such phyletic persistence suggests that they have physiological
functions, but currently it is unknown what they may be.
The neurohypophysial hormones are nonapeptides, which, as described earlier,
are synthesized in the cell bodies of the supraoptic and paraventricular nuclei
in the hypothalamus of mammals, birds and reptiles. In amphibians and fish
they are formed in the preoptic nucleus. Chemically, neurohypophysial peptides
consist of a ring structure containing six amino acids which is closed by a disul-
phide bond contributed by two hemi-cystines. There is also a side chain consist-
ing of three amino acids (Fig. 2.5). Vasopressin has phenylalanine at position 3
and either arginine or lysine at position 8. Oxytocin differs from vasopressin by
two amino acid substitutions and has isoleucine at position 3 and leucine at posi-
tion 8. In non-mammals, vasotocin replaces vasopressin. Like oxytocin, it has
isoleucine at position 3 but retains arginine at position 8, as in vasopressin. Hence

62
 Amino acid position 2 3 4 5 6 7 8 9
Common structure,
variations In positions
3,4and8
Neurohypophysial
hormone
8-Arg-vasopressln cts-Tyr-Phe-Gin-Asn-C~s-Pro-Arg-Giy (NH 2)
Mammals
8-Lys-vasopressln Lys
Pigs, some marsupials
Oxytocin lie Leu
Mammals, Holocephali
8-Arg-vasotocln lie Arg
All nonmammals
Mesotocln lie lie
Birds, reptiles, amphibians,
lungfish, some marsupials
lsotocln lie Ser lie
Teleost& and some other
bony fish
Glumltocln lie Ser Glu
Skates and rays
Valltocln lie Gin Val
Sharks

Fig. 2.5. The amino acid sequences and phyletic distribution of the major neurohypophysial
hormones in vertebrates. (Based on information summarized by Acher 1996 and Acher et a!.
1970, 1999)

it is called vasotocin. Its effects are less specific than those of vasopressin as it not
only has antidiuretic and vasoconstrictor effects but also exerts oxytocic actions
on the uterus and oviduct. When tested in mammalians it can also promote milk
letdown. This hormone has been identified in agnathan fish, where it appears to
be the sole such neurohypophysial peptide. Vasotocin may be the primordial neu-
rohypophysial hormone in vertebrates. The lineage of such peptides may go back
even further, as structural homologues, conopressin and cephalotocin, have been
identified in molluscs (Van Kesteren et al. 1992a,b ).
In tetrapods, vasopressin and vasotocin are released in response to increases
in the osmotic pressure of the plasma. An osmoreceptor complex is associated
with the hypothalamic neuronal nuclei. However, vasopressin and vasotocin may
also be secreted in response to other stimuli, including a reduction in blood
volume and stress. Several distinct receptors for the neurohypophysial hormones
have been identified in mammals. There is an oxytocin receptor, a vasopressin
V 1• receptor, which mediates the contraction of vascular muscle and a V2 receptor,
which is responsible for increases in the permeability of the renal tubule
to water. The receptors in rats have been cloned and contain about 400 amino
acid residues. They belong to the G-protein-coupled receptor superfamily
(Birnbaumer et al. 1992; Kimura et al. 1992; Lolait et al. 1992; Morel et al. 1992).
The vasotocin receptor in a teleost fish, the white sucker, has also been cloned
(Mahlmann et a1. 1994). It contains 435 amino acid residues, the sequence of which

63
has a 61% identity to the rat V 1a receptor and a 42% identity to the V2 receptor. It
interacts not only with vasotocin but also vasopressin and even molluscan cono-
pressin. However, it does not bind to isotocin, which is the other oxytocin-like
hormone in teleosts. Responses to V1a receptors are mediated by the phospholi-
pase C-phosphatidylinositol system and those to V2 receptors by the adenylate
cyclase-CAMP mechanism.

The Growth Hormone-Prolactin Family. Growth hormone (somatotropin) and

prolactin belong to the same family of protein hormones, which also includes
several placental lactogens and somatolactin (Nicoll et al. 1986; Wallis 1992;
Aramburg et al. 1997). The latter has been identified in the pars intermedia of
several groups of bony fish. Growth hormone and prolactin contribute to the
adaptation of some teleost fish to changes in the osmotic concentrations of their
external environments. Growth hormone has ubiquitous effects in the regulation
of growth and the metabolism of fats, carbohydrates and proteins. It can influ-
ence such processes in many tissues. Prolactin has many different effects, which
involve tissue differentiation including milk production by the mammary glands,
crop sac secretion in some birds, metamorphosis in larval amphibians and cuta-
neous changes which occur in newts during their breeding migration to fresh
water. In 1956, D. C. W. Smith found that the administration of growth hormone
to brown trout increased their ability to adapt and survive transfer from fresh
water to sea-water. In 1959, Pickford and Phillips demonstrated that euryhaline
killifish failed to survive transfer from sea-water to fresh water after they had been
hypophysectomized. However, this ability was restored by the administration
of prolactin. It is now known that these effects of the two hormones in fish are
principally due to their actions on exchanges of sodium chloride and water across
their gills. Urodele amphibians exhibit the so-called newt water-drive response
to injected prolactin, and migrate to their breeding ponds (Chadwick 1940).
Prolactin has been shown, in such amphibians, to decrease the permeability of
their skin to water and Na+ (Brown and Brown 1973).
Growth hormone and prolactin are synthesized in the somatomammotrope
cells of the adenohypophysis. They are related proteins that are present in all ver-
tebrates, with the apparent exception of agnathan fish. Growth hormone consists
of about 190 amino acids and contains two cross-linking disulphide bonds. Pro-
lactin usually has about 200 amino acids, though there are fewer such residues in
the hormones of some fish. In most species prolactin contains three disulphide
bonds but there are only two in teleost prolactin and in the bowfin (Holostei).
However, in the sturgeon (Chondrostei), which is considered to be a phyletic pre-
decessor of the teleosts and the bowfin, there are three such disulphide bonds.
Prolactin in lungfish (Dipnoi) also contains three disulphide bonds. Many amino
acid substitutions occur in the molecules of growth hormone and prolactin, but
they each retain five common domains and have similar gene architectures. It has
been suggested that they share a common ancestry and arose from a single growth
hormone-like gene (Chen et al. 1994). Cattle growth hormone has a 67% homol-
ogy in its amino acid sequence to that of the human hormone, but in salmon this
similarity is only 34%. Cattle prolactin has a 76% homology to that in humans

64
but when compared to salmon this value is 35%. Despite such structural differ-
ences, there is usually a considerable crossover in the abilities of such hormones
to act, when injected, in other species. Chen and his collaborators ( 1994} have sug-
gested that this family of hormones originated from a gene that was present in a
deuterostome ancestor of the vertebrates. They also consider that the primaeval
gene product may have had a role in the osmoregulation of such invertebrates,
possibly contributing to the mobilization and transport of organic osmolytes,
derived from their nutrients.
The synthesis and release of growth hormone in fish has been described as
multifactorial (Peter and Chang 1997}. However, basal levels of the hormone
appear to be regulated from the hypothalamus by the stimulatory actions of
GH-RH and inhibitory ones of somatostatin. Dopamine also exerts a stimulatory
effect on the release of growth hormone in teleosts. The secretion of prolactin in
vertebrates is predominantly under the inhibitory control of dopamine (Sharp
1997}. However, peptides with a stimulating effect on the release of prolactin may
also be present. Thus, TRH has been observed to stimulate the release of prolactin
in amphibians. In some euryhaline teleosts the release of prolactin may result
from the direct effects of decreases in the osmotic concentration of the extracel-
lular fluid (Grau et al. 1994}.
Most of the effects of growth hormone are mediated by a growth factor,
which it induces in the liver and some other tissues. It is called insulin-like growth
factor-I (IGF-I) and it belongs to the insulin hormone family. Human IGF-1 con-
tains 70 amino acids and it has a 35% homology in its amino acid sequence to
insulin. Insulin-like growth factor-1 has been identified in all groups of verte-
brates, and its structure is highly conserved. Salmon IGF-I has an 80% homology
to human IGF-I. Insulin-like growth factor-I has mitogenic effects and its many
target tissues include the gills of fish. Its receptors, which are present in the cell
membrane, belong to the insulin receptor tyrosine kinase family.
Cell membrane receptors for the growth hormone-prolactin family of
hormones belong to the cytokine receptor superfamily (Bazan 1990; Nakagawa et
al. 1994). It also includes receptors for several cytokines.

Adrenocorticotropic Hormone. The adrenocorticotropic hormone (ACTH, cor-

ticotropin) stimulates and maintains the steroidogenic activity of adrenocortical
tissue. It principally influences the synthesis of cortisol and corticosterone. Its
relationship to osmoregulation is generally indirect. This hormone is present in
the pituitary of all groups of vertebrates. It is formed from the prohormone, proo-
piomelanocortin, in the corticotrope cells of the adenohypophysis. The adreno-
corticotropic hormone contains 39 amino acid residues. Interspecific differences
principally occur in a C-terminus "tail" region. The amino acids are invariant at
19 positions, 18 of which are present near the N-terminus of the molecule. Release
occurs in response to stimulation by CRH from the hypothalamus and, in stress-
ful situations, also vasopressin. Various cytokines, including some interleukins
and tumour necrosis factor-a, can also stimulate release of ACTH. Cortisol and
corticosterone exhibit negative feedback effects, both in the hypothalamus and
on the corticotropes in the pars distalis, and inhibit release.

65
2.2 The Renin-Angiotensin System (RAS)

Angiotensin II is an octapeptide hormone with several important roles in the

processes of osmoregulation (Laragh and Sealey 1992; Kobayashi and Takei 1997;
Fitzsimons 1998). It is formed from a precursor in the plasma, the globulin protein
angiotensinogen, as a result of the action of renin, which is secreted by the kidney.
A decapeptide, angiotensin I, is initially formed, which is subsequently"activated"
by angiotensin-converting enzyme (ACE) to form angiotensin II. This peptidase
enzyme is mainly associated with the pulmonary blood vessels. Angiotensin
II is a powerful vasoconstrictor and can increase blood pressure. It can also
promote sodium retention by the kidney and gut by stimulating the secretion of
aldosterone by adrenocortical tissue. The latter steroid hormone promotes the
reabsorption of Na+ from the fluids in the renal tubule and colon. Angiotensin II
may also have direct effects on Na+ reabsorption at these sites. It also can act
in the hypothalamus, to induce the sensation of thirst and salt appetite and
promote the release of vasopressin. Thus, the overall effect of angiotensin
II on osmoregulation is to maintain the volume and the composition of the
extracellular fluid.
Renin is secreted by the kidneys. It is a glycoprotein protease enzyme that is
formed in the granulated juxtaglomerular cells of the afferent glomerular arteri-
ole. These are epithelioid cells, which in mammals, and probably in birds, lie near
the macula densa. The latter group of cells are present in the wall of the adjacent
distal renal tubule. Together with a tuft of tissue that is associated with the
glomerulus, the extraglomerular mesangium (or polkissen), these two types of
cells make up the juxtaglomerular apparatus. This tissue association is apparently
present only in mammals, birds and, somewhat unexpectedly, elasmobranch fish
(Lacy and Reale 1990). However, the granulated juxtaglomerular cells, which
secrete renin, have been identified throughout the vertebrates, with the apparent
exception of agnathan fish. Isorenins occur in other tissues, including the brain,
cardiovascular system and uterus.
Angiotensinogen (renin-substrate) is an a2-globulin, which is synthesized in
the liver and is present in the blood plasma. It contains 453 amino acid residues
of which the first 10, at the N-terminal, are split off, as a result of the action of
renin, to form angiotensin I. As described above, this peptide is converted to
angiotensin II [angiotensin-(1-8)] by ACE. Other angiotensin peptides are also
formed as a result of the actions of peptidase enzymes including angiotensin III
[angiotensin-(2-8)] (Blair-West et al. 1971). It has a much weaker vasoconstric-
tor action than angiotensin II, but has a similar ability to stimulate aldosterone
synthesis. Angiotensin-(1-7), under experimental conditions, can antagonize the
effects of angiotensin II and increase urinary sodium excretion (Handa et al.
1996). Its possible physiological role has not been defined. Homologous forms
of angiotensin I have been identified in many vertebrates (Fig 2.6). In most fish,
except the bowfin, asparagine is present at position 1 (fish angiotensin). In the
tetrapods, aspartic acid is present at this site. Many amino acid substitutions have
been observed at position 9, which is the site of action of ACE. A notable and
unique amino acid substitution is that of proline for valine at position 3 in the
elasmobranch angiotensin I.

66
 Amino acid position 2 3 4 5 6 7 8 9 10
Common structure,
variations in positions
1,3and9

Angiotensin I

Cattle Asp- Arg- Val- Tyr- Val- His- Pro- Phe- His- Leu
Domestic fowl Ser
Turtle His
Bullfrog Asn
Lungfish Asn Thr
Salmon Asn Asn
Eel Asn Gly
Bowfin Asn
Dogfish Asn Pro Gin

Angiotensin II

Fig. 2.6. The amino acid sequences of angiotensin I from different vertebrates. (Based on infor-
mation given by Takei et al. 1993, 1998 and Joss eta!. 1999)

The activation of the renin-angiotensin system begins with the release of renin
from the juxtaglomerular cells in the kidney. This event can occur in response to
several stimuli. Baroreceptors associated with the afferent glomerular arteriole
can sense a drop in hydraulic pressure and trigger release. The macula densa
(Schuermann 1998) can detect changes in the sodium chloride (especially Cl")
concentrations in the distal renal tubular fluid and transmit this information
to the adjacent juxtaglomerular cells. A decrease in the renal tubular concentra-
tion of sodium chloride results in an increased secretion of renin. Conversely,
increases in sodium chloride concentration or a rise in hydraulic pressure
inhibit release. The juxtaglomerular cells have sympathetic nerve supply and ~­
adrenergic receptors. Neural stimuli originating in the brain can trigger a release
of renin in this way.
Angiotensin II can constrict local intrarenal blood vessels, including the affer-
ent and efferent glomerular arterioles and vasae rectae. It may thus influence the
GFR and renal medullary solute concentration gradients. However, the possible
physiological relevance of such effects on urinary Na+ excretion and urine con-
centration is not clear. Angiotensin appears to have other physiological roles,
apart from maintaining the integrity of the extracellular fluids. The presence of
a renin-angiotensin system in the brain suggests that it may function as neuro-
transmitter, and it could be contributing to such functions as cognition and
memory (Mosimann et al. 1996).
Several types of angiotensin receptors have been identified in various tissues
(Wright et al. 1995; Nishimura et al. 1997). They are associated with the cell mem-

67
brane. The AT 1 and AT2 receptors have been cloned. An AT 1-like receptor has been
identified in birds, amphibians and teleost fish. The AT 1 receptors mediate the
responses related to the maintenance of the integrity of the extracellular fluids,
including cardiovascular actions. These effects are transduced by the phospholi-
pase C-phosphatidylinositol mechanism.
The actions of angiotensin II on the cardiovascular system, kidney function,
thirst and corticosteroidogenesis have been observed in most groups of the ver-
tebrates (Nishimura 1987; Joss et al.1994; Hanke 1997; Kobayashi and Takei 1997).
However, possible roles in the agnathan fish are in doubt.

2.3 Adrenocorticosteroids

The adrenocorticosteroid hormones, which have been identified in all groups of

the vertebrates, have two major types of effects. They contribute to the regulation
of the metabolism of proteins, fats and carbohydrates. These effects are called
their glucocorticoid actions. They also help regulate the concentrations of sodium
and potassium ion the body. Such effects are known as their mineralocorticoid
actions. These steroid hormones occur throughout the vertebrates. In tetrapods
they promote the retention of sodium and excretion of potassium. In marine
teleost fish, salt excretion across the gills is increased.
In mammals, adrenocorticosteroids are secreted by the adrenal cortex. The
adrenal gland lies near the kidneys. In most mammals it is divided into a distinct
outer cortex, which secretes steroid hormones, and an inner medulla composed
of chromaffin tissue, which secretes adrenaline and noradrenaline. This type of
zonation does not occur in other vertebrates, though an intermingling of the two
types of tissues occurs in most species. However, in some fish, including elasmo-
branchs and agnathans, they each occupy separate sites. In the elasmobranchs the
steroidogenic tissue forms distinct aggregates that lie between the kidneys and
are called the interrenal glands. In most mammals the cortical tissue is arranged
in three layers; an outer zona glomerulosa, an underlying zona fasciculata and an
inner zona reticularis.
Adrenocorticosteroids are so named because of their site of origin in
mammals. As such hormones are also secreted by homologous (adrenocortical or
interrenal) tissue in other vertebrates, this generic name has been retained.
However, the shorter version, corticosteroids, is used more often. The particular
chemical type of steroid hormone and its relative abundance may vary in the
different groups of vertebrates (Henderson and Kime 1987). Mammals secrete
aldosterone, which is the prototypical mineralocorticoid, and also cortisol and
corticosterone (Fig. 2.7; Table 2.3). The latter two steroids generally function as
glucocorticoids. However, these steroids in sufficient concentration can also
exhibit mineralocorticoid effects. In teleost fish, cortisol acts as both a glucocor-
ticoid and mineralocorticoid. In birds, reptiles and amphibians, the predominant
corticosteroid hormones are aldosterone and corticosterone. In teleost fish, cor-
tisol predominates though in some species small amounts of corticosterone and

68
 Phyletic distribution
Cortisol
Most mammals, bony fish,
including teleosts, lungfish
and Holocephali, and
hagfish

Corticosterone
Some mammals, birds,
reptiles, amphibians,
lungfish and hagfish

Aldosterone
Tetrapods and lungfish
(small amounts in a few
teleosts)

1a-Hydroxycorticosterone
Elasmobranch fish
(sharks and rays)

Fig. 2.7. The chemical structures and phyletic distribution of adrenocorticosteroid hormones
in vertebrates

even aldosterone have been identified. Elasmobranchs possess a unique such

hormone, !a-hydroxycorticosterone. This steroid is not present in their carti-
laginous relatives the Holocephali, which, instead, have cortisol. Lungfish, like
tetrapods, secrete relatively large amounts of aldosterone as well as cortisol and
corticosterone.
The synthesis of corticosteroid hormones from cholesterol can be increased
by ACTH and angiotensin II and inhibited by natriuretic peptides. Elevated
concentrations of K+ in the plasma can also directly promote such synthesis.
The relative importance of the effects of the tropic hormones in the different
phyletic groups of vertebrates varies. In mammals, ACTH is especially impor-
tant in promoting cortisol and corticosterone synthesis. This process occurs in
the zona fasciculata. Angiotensin II acts in the zona glomerulosa to increase
the synthesis of aldosterone. In other groups of vertebrates, both these tropic
hormones can exert more general effects and often promote the synthesis of all
corticosteroids.
The target organs and tissues that mediate the mineralocorticoid effects of the
corticosteroids vary in different species. In mammals, aldosterone promotes Na+
absorption and K+secretion across the renal distal tubule-collecting duct system.
A similar effect is seen in the colon of most tetrapods and the sweat glands and
salivary glands of mammals. The kidneys of birds, reptiles and possibly amphib-
ians are also responsive. Aldosterone promotes the absorption of Na+ across the

69
Table 2.3. The predominant adrenocorticosteroid hormones in the vertebrates

Cortisol (F) Corticosterone (B)' Aldosterone

Mammals
Placentals + +
Rats, mice, rabbits + +
Marsupials + A few species +
Monotremes
Echidna + +
Platypus + +
Birds + +
Reptiles + +
Amphibians + +
Fishes
Osteichthyes
Dipnoi (lungfish) + +
Teleostei A few?
Holostei (bowfin) +
Chondrostei (sturgeons) +
Chondricthyes
Elasmobranchii 1a- hydroxycorticosterone
Holocephali (chimaeroids) +
Agnatha
Myxiniformes
(hagfish) + +
References: Henderson and Kime (1987).
Marsupials: Oddie et al. (1976); McDonald and Martin (1989).
Monotremes: Weiss and McDonald (1965); McDonald et al. (1988).
' Small amounts of corticosterone, high FIB, are often present in the plasma of species where
cortisol is predominant.
b Cortisone is also often present in the plasma.

(Androgens are secreted by the adrenal cortex of mammals.)

skin and urinary bladder of amphibians. Cortisol can promote the uptake of Na+
across the gills of teleost fish in fresh water and stimulate salt excretion by the
same route in sea-water.
Two types of receptors for corticosteroids have been identified, principally
in mammals but also in some other species, especially amphibians. They are
present inside cells, usually in the region of the nucleus. They have been charac-
terized, and named, glucocorticoid receptors (GR, Type I) and mineralocorticoid
receptors (MR, Type II). In teleost fish one type of receptor mediates both types
of effects (Sandor et al. 1984). It has been cloned (Ducouret et al. 1995) and
appears to have originated from a GR-like receptor prior to the origin of the tetra-
pod GRs. The corticosteroid receptors, when combined with their hormonal
ligands, initiate genetic transcription and translation. Mineralocorticoid-type
effects can involve such processes as the synthesis, activation and translocation
of Na-K-ATPase and ion channels, especially the epithelial sodium channel or
EN a C.

70
2.4 Adrenaline and Noradrenaline

Adrenaline (epinephrine) and noradrenaline (norepinephrine) are secreted by

endocrine chromaffin tissue in all vertebrates. Embryonically, this tissue is
derived from neural ectoderm. In mammals, it forms the adrenal medulla that is
equivalent to a collection of postganglionic nerve cells of the sympathetic nervous
system. The adrenal medulla retains the preganglionic cholinergic nerve connec-
tion to the sympathetic nervous system. Noradrenaline is the principal neuro-
transmitter of postganglionic sympathetic nerves and is a metabolic precursor of
adrenaline. The latter is usually the predominant secretion of the adrenal medulla.
Hormonal adrenaline and noradrenaline can mimic the effects of stimulation of
the sympathetic nervous system. Their release constitutes part of the overall sym-
pathetic response, such as occurs in response to stress. This effect is an adapta-
tion to noxious physical and emotional events and can influence osmoregulation.
Such adrenergic responses include vasoconstriction, vasodilatation and increases
in blood pressure that can influence the functioning of such organs as the kidneys,
skin and gills. A tissue mobilization of glucose (glycogenolysis) and fatty acids
(lipolysis) supplies additional energizing metabolic substrates. Adrenaline and
noradrenaline also can have direct modulating effects on the secretion of exocrine
and endocrine glands, including sweat glands and the neurohypophysis, where a
release of vasopressin occurs. In the gills of fish and skin of amphibians the trans-
port of ions and permeability to water may be changed.
Adrenaline and noradrenaline (Fig 2.8), and also dopamine, are called cate-
cholamines due to the presence of a catechol moiety (dihydroxybenzene) in their
chemical structures. They are synthesized enzymatically from phenylalanine
or tyrosine. The structures of these catecholamines are constant throughout the
vertebrates and they are also present in invertebrates and even some plants.

HQ.
Adrenaline HO-©·CHOH-CH2-NHCH3

HO-Q>
HO,
Noradrenaline -CHOH-CH.-NH•

HO,

Dopamine HO·©·CH 2-~H-NH2

COOH

Ho/Q-
1 I N~

Triiodothyronine (T.) 0 -© -CH2-~H-COOH

'I' I
I In Thyroxine (T4)

Fig. 2.8. The chemical structures of the catecholamine and thyroid hormones in vertebrates

71
 The effects of the catecholamine neurotransmitters and hormones are medi-
ated, and differentiated, by a variety of subtypes of receptors that are present
in the cell membrane. Vasoconstriction is the result of stimulation of a 1- and
O.z-adrenergic receptors and the rate and force of contraction of the heart of
~~- and ~z-receptors. The release of renin is mediated by a 1- and ~ 1 -adrenergic
receptors and that of vasopressin by ~ 1 -receptors. Changes in the movements
of ions and the osmotic permeability of the gills of fish can involve both a- and
~-adrenergic receptors. The cellular mechanisms mediating such responses
include the adenylate cyclase-cAMP system for stimulating effects mediated
by ~-receptors and inhibitory effects mediated by a 2-receptors. The phospholi-
pase C-phosphatldylinositol system mediates responses involving a 1-adrenergic
receptors.

2.5 The Natriuretic Peptide Hormones

In 1981, de Bold and his associates identified a hormonal product of mammalian

atrial heart muscle that promoted the excretion of sodium by the kidney (de Bold
1985). The possible existence of a natriuretic hormone had been the subject of
much earlier speculation, but its origin in atrial heart muscle was an endocrine
surprise. The secretion was called, variously, atrial natriuretic peptide (ANP),
atrial natriuretic factor and atriopeptin. Several other related "peptides" have
been identified in the brain of many vertebrates. They also appear to be present
in invertebrates, such as in the hearts of oysters and blue crabs (Poulos et al. 1995).
In mammals, ANP acts on the kidney, where it increases urine flow and sodium
excretion (natriuresis) (Brenner et al. 1990; Atlas and Maack 1992). It is also a
powerful vasodilator. Such effects have been observed throughout the vertebrates
(Takei and Balment 1993). Natriuretic peptides can also promote salt loss in
marine fish by stimulating its extrusion from the gills of teleost fish and secre-
tion by the rectal salt gland in elasmobranchs. The general effects of the natri-
uretic pep tides appear to counteract expansion of the extracellular fluid space due
to the excessive accumulation of sodium.
The chemical structures of the natriuretic peptides (Atlas and Maack 1992;
Takei 1994) all include a ring configuration containing 17 amino acid residues
joined by a disulphide bridge provided by two hemicystines. ANP contains 28
amino acids, 6 at theN-terminus precede the ring structure and 5 form a "tail" at
the C-terminus (Fig. 2.9). The amino acid sequences in the ring structures of dif-
ferent species are highly conserved. However, there are considerable differences
in the remainder of such molecules, depending on the species and the tissue site
of its origin. The various natriuretic peptides have been classified into three main
groups (Fig. 2.9). Type A, which includes mammalian ANP-28; type B (BNP),
which is found in the brain as well as heart muscle; and type C (CNP), which is
mainly present in the brain. A fourth type has been identified in the heart ven-
tricular muscle of teleost fish. It has an elongated tail containing 14 amino acid
residues at its C-terminus. Interspecific variations in their amino acid sequences
suggest that type-B natriuretic peptides are the least conserved and type C are

72
 Type A ( ANP-28) Ser-Leu-Arg-Arg-~-Ser Cys-Phe-GI~-Giy-

Type B ( BNP-32) Ser-Pro-Lys- Thr-Met-Arg-Asp-Ser-Giy Cys-Phe-Giy Arg-

Type C ( CNP-32) Gly-Leu-Ser-Lys-Giy Cys-Phe-Giy Leu-

28
·Arg-Met Asp-Arg-lle-Giy Ala-Gin ser-Giy-Leu-Giy-Cys Asn-lli-Phe-~-- -It!.

32
- Arg-~ Asp-Arg-lle-Giy ~-Leu Ser-Giy-Leu-Giy-Cys Asn-Vai-Leu-~-Arg- Tyr

22
- Lys-Leu-~sp-Arg-lle-Giy Ser-Met- Ser-Giy-Leu-Giy-Cy

Fig. 2.9. Amino acid sequences of the atrial natriuretic peptides (type A, type Band type C). The
boxed sections indicate identical sequences within the ring structure in all three types of the
hormones. The underlined residues indicate homologies in two of the types. * replaced by
isoleucine in some mammals. Type B may have an extended N-terminus to give, for instance,
BNP-32 (as shown), BNP-26 in the domestic pig and BNP-45 in rodents. (After Atlas and Maack
1992)

the most conserved. Elasmobranch brain CNP has an 85% identity of its amino
acid sequence with its counterpart in mammals (Suzuki et al. 1992). A unique
natriuretic peptide has also been identified in the mammalian kidney (Goetz
1991). It has been called urodilatin, but its possible physiological role is unknown.
A peptide, containing 29 amino acids, has been identified in the heart of Atlantic
salmon that appears to be related to the A-, B- and C-types of natriuretic pep tides
found in other species (Tervonen et al. 1998). However, it is distinct, and it has
been suggested that it could be an ancestral type of such peptides.
Natriuretic peptides in mammalian heart muscle are released in response to
expansion of the plasma volume that results in the activation of stretch receptors
in the right atrium (Thibault et al. 1999). Volume expansion of the extracellular
fluids also promotes such a release in teleost and elasmobranch fish. In teleosts,
hyperosmotic stimuli may also increase such secretion.
The natriuretic and diuretic actions of the natriuretic peptides can involve
several types of effects and mechanisms. Increases in the GFR, such as could be
mediated by a dilatation of the afferent glomerular arterioles, could be involved.
However, aglomerular teleost fish also exhibit such renal effects. Natriuretic pep-
tides can inhibit the synthesis of aldosterone, which would be expected to result
in a decreased reabsorption of sodium from the renal tubule. A direct blockade

73
of sodium channels in the apical cell membrane of the renal tubule may also
occur. The infusion of ANP has also been observed to increase the movement of
fluid and proteins across the capillary bed (Renkin and Tucker 1996). Such an
effect would be expected to decrease the plasma volume. Natriuretic pep tides have
been shown to decrease the release of vasopressin, which could be contributing
to the observed diuretic effects.
Three types of membrane receptors have been identified that can bind
natriuretic peptides. They are present in a variety of tissues including blood
vessels, kidney, adrenal, brain and the gills of fish. Two of these receptors are
linked to guanylate cyclase and are called GC-A and GC-B. The former interacts
with ANP and BNP and the latter with CNP. Such binding results in an activation
of the guanylate cyclase (Chinkers et al. 1989). The third type of receptor binds
natriuretic peptides but does not appear to be linked to known responses. It has
been called a clearance, or C-type, receptor. A more definitive role for it may yet
emerge.

2.6 Adrenomedullin

In 1993, Kitamura and his associates (Kitamura et al. 1993a) described a polypep-
tide in a human adrenal medullary tumour (a phaeochromocytoma) that had
a powerful vasodilatatory effect and decreased the blood pressure of rats. It
was also found in normal adrenal medulla and a number of other tissues includ-
ing, kidneys, heart, intestine, pituitary gland and the hypothalamus (Kitamura
et al. 1995). However, its concentrations are much higher in the adrenal medulla.
It is also present in blood, and it has been suggested that it may function as a
hormone.
Apart from its vasodilatatory effect, adrenomedullin has a number of other
actions that may influence osmoregulatory processes (Samson 1999; Samson
et al. 1999). They include diuretic and natriuretic effects on the kidneys, and an
inhibition of thirst and salt appetite, which is mediated in the hypothalamus.
Adrenomedullin can also inhibit the release of ACTH, vasopressin and aldos-
terone. Its presence in the blood has been related to diseases such as congestive
heart failure, that result in an expansion of the extracellular fluid volume (Cheung
and Leung 1997). Such observations strongly suggest that adrenomedullin has a
physiological role in the regulation of fluid volume in the body.
Human adrenomedullin is a polypeptide containing 52 amino acid residues
that incorporate a six-membered ring structure closed by a disulphide bridge
(Kitamura et al. 1993a,b). Its precursor, proadremomedullin, consists of 164
amino acid residues. Adrenomedullin has a structural similarity to calcitonin-
gene-related peptide (CGRP, a neuropeptide) and amylin (secreted by the B-cells
of the islets of Langerhans). These molecules have even been observed on occa-
sion to interact with each other's receptors and are considered to be members of
the same superfamily (Wimalawansa 1996). Interspecific differences have been
observed in the structures of adrenomedullin. Thus, the rat polypeptide has only
50 amino acids and differs from that in humans by six amino acid substitutions.

74
Adrenomedullin-like immunoreactivity has been identified in the nervous sys-
tem of an echinoderm, suggesting that it may have a long phylogenetic history
(Martinez et al. 1996).
TheN-terminus of proadrenomedullin includes a 20-membered peptide that
also exhibits biological activity (Kitamura et al. 1993b; Samson 1998). It is called
proadrenomedullin N-terminal peptide or ProAM-N20 peptide (PAMP). Like
adrenomedullin, it can decrease blood pressure and inhibit the release of ACTH
and aldosterone. However, its vasodilatatory action is mediated by a decrease in
neural sympathetic activity, including inhibition of release of adrenaline.
The effects of adrenomedullin on the kidney are associated with an increased
renal blood flow and GFR, and decreased sodium reabsorption from the distal
renal tubule {Jougasaki et al. 1995). Receptors for adrenomedullin are associated
with the renal distal convoluted tubules {Jensen et al. 1998). It is possible that it
is exerting a local, paracrine, effect in the kidneys. Its vascular effects appear to
be mediated by the formation of nitric oxide (NO) by the vascular endothelium.
However, the mechanism of its action of the renal tubule is unknown. In blood
platelets it has been observed to increase the production of cAMP (Kitamura
et al. 1993b).

2.7 Guanylin Peptides

The guanylin pep tides are a recently discovered group of putative hormones that
can promote the secretion of cl- and HC0 3- by the intestinal mucosa (Forte and
Hamra 1996; Forte et al. 2000). They also have diuretic, natriuretic and kaliuretic
effects on the mammalian kidney. Their discovery arose from the observations
of M. Field and his collaborators {1978) on the causes of watery diarrhoea in
humans. This disease results from infections by Escherichia coli bacteria. A heat-
stable enterotoxin was isolated from incubates of these bacteria that increased
intestinal secretion of cl-. This response was associated with an increase in tissue
cGMP, which was apparently formed as a result of a stimulation of intestinal
guanylate cyclase. The bacterial enterotoxin (ST, for stable toxin) contains 16
amino acid residues, including six cysteines that form three disulphide bonds. A
search for endogenous homologues of this toxin uncovered three related pep tides;
guanylin, uroguanylin (originally found in the urine of the opossum) and lym-
phoguanylin. They contain 15 or 16 amino acids. Guanylin and uroguanylin have
two disulphide bonds and lymphoguanylin one. The bacterial enterotoxin mimics
the effects of the guanylins in the intestine. The homology of the amino acid
sequences in uroguanylin and bacterial ST is 69%.
Guanylin peptides are produced in the intestinal mucosa by the enterochro-
maffin cells. Lymphoguanylin appears to be synthesized in lymphoid tissue (Forte
et al. 1999). There are interspecific variations in the structures of the guanylins.
Human and opossum uroguanylins have a homology of 80% in the sequences of
their amino acid residues. This value is 73% for their guanylins. Uroguanylin
appears to be more active than guanylin, possibly reflecting a greater resistance
to enzymatic inactivation.

75
 Guanylins have been identified in the blood and are also secreted into the
intestinal lumen. The precise stimuli for their release do not appear to have been
defined, but it has been suggested that secretion occurs postprandially and
reflects the sodium chloride content of the food. Their excretion in the urine is
increased by a high salt diet.
Two types of receptors have been identified for guanylins; in the intestinal
mucosa and the proximal renal tubule of the opossum. They are present in the
cell membrane, where they are associated with membrane guanylate cyclase. The
responses to guanylin are mediated by cGMP and may involve an interaction with
cGMP-dependent protein kinase II (PKG II) or even cAMP-dependent protein
kinase II (PKA II). The subsequent protein phosphorylation may involve activa-
tion of ion channels, including the CFTR chloride channel.

2.8 The Thyroid Hormones

A thyroid gland or homologous follicular tissue is present in all vertebrates and

the chemical structures of its secretions are identical in all species. They are
iodine-containing derivatives of tyrosine (Fig. 2.8}. Thyroxine contains four
iodine atoms (hence it is referred to as T4 ) and triiodothyronine three (T3 ).
The latter has the predominant hormonal activity, but T4 can be deiodinated
at the 51 position in peripheral tissues, by monodeiodinase enzymes, to Form
T3 • Thyroxine thus functions mainly as a prohormone. The final synthesis of
thyroid hormone takes place in the follicles of the thyroid gland. The process can
be regulated by adenohypophysial thyroid-stimulating hormone (TSH, thy-
rotropin), the release of which is partially under the control of TSH-releasing
hormone (TRH) from the hypothalamus. Synthesis involves the 'prohormone' thy-
roglobulin, which is a large tyrosine-containing protein that accumulates in the
thyroid follicles. Iodide is actively accumulated by the thyroid cells from the blood
and, following its oxidation to iodine, is utilized to iodinate specific sites on the
tyrosine residues.
Thyroid hormone has ubiquitous actions in the body, which usually have only
indirect effects on osmoregulation (Grau 1987}. In mammals and birds, cell
metabolism and oxygen consumption are increased by thyroid hormone (calori-
genic effect). This effect can result in increased evaporative water losses. A stim-
ulation of oxygen consumption has been sporadically reported in cold-blooded
vertebrates, but such an effect does not appear to be a general one in such species.
Thyroid hormone also can promote cell proliferation and differentiation in many
vertebrates (morphogenetic effect). A dramatic example of this action is the pro-
motion of metamorphosis by amphibian tadpoles into juvenile adults. Such a
metamorphosis is also seen in some fish, such as flounder.
The activity of the thyroid gland and plasma thyroid hormone concentrations
increase during the transformation of freshwater salmonid parr to smolt (Hoar
1951; Prunet et al.1989). The latter can then migrate and adapt to life in the sea. This
ability is associated with the differentiation of salt-secreting chloride cells in their
gills. However, as will be described later, other hormones also contribute to this

76
process. Metamorphosis in amphibians is associated with the ability to adapt to a
terrestrial life. This process results in many changes, such as involve the function-
ing of the skin and an ability to respond to neurohypophysial hormones (Howes
1940; Bentley and Greenwald 1970 ). In mammals, thyroid hormone has been shown
to increase the levels of Na-K-ATPase in the kidney (Ismael-Beigi 1993 ).

2.9 The Urotensins

Urotensin I and II are peptides that have been identified in large spinal cord
neurons (Dahlgren cells) in a wide variety of fish, including teleosts and elasmo-
branchs. They exhibit a number of actions, including an ability to influence the
contractility of vascular and urinogenital smooth muscle (hence their names).
Urotensins can change the rate of salt transport across some epithelial mem-
branes. In teleosts, the spinal cord neurons often aggregate in the tail region to
form a gland-like structure called the urophysis (Arsaky 1813). Such a structure
has been identified in over 400 species of teleost fish (Fridberg and Bern 1968;
Kobayashi et al. 1986). Changes in its histological appearance have been observed
following transfer of such fish between fresh water and sea-water (Enami 1955).
These observations resulted in the suggestion that it may be contributing to their
osmoregulation (see Larson and Bern 1987). However, such a role, while consid-
ered likely, has not yet been clearly established. Secretion from the urophysis
could have other functions and be contributing to the functioning of the cardio-
vascular system and reproduction. Urotensin I is a polypeptide containing 41
amino acid residues. Its structure is similar to that of mammalian corticotropin-
releasing hormone (CRH), which is present in the hypothalamus (Lederis et al.
1994; Vaughan et al. 1995). It has been classified as a member of the CRH family
of neuropeptides that have a widespread distribution in vertebrates (Lovejoy and
Balment 1999). Urotensin II consists of 12 amino acid residues and exists in at
least 15 different but homologous forms (Fig. 2.10). It is usually present in the

Amino acid position 2 3 4 5 6 7 8 9 10 11 12

Common structure,
varatlons In
positions 1, 2, 3, 4, 5

Urotensln II

Lamprey Asn-Asn-Phe-Ser-Asp-Cys-Phe-Trp-Lys-Tyr-Cys-Val
Dogfish

Sturgeon Gly Ser Thr Glu

Trout Gly Gly Asn Glu
Flounder Ala Gly Asn Thr Glu
Goby Ala Gly Thr Ala

Fig. 2.10. The amino acid sequences of urotensin II from various fish. (Based on information
given by Waugh and Conlon 1993 and Waugh et al.l995)

77
urophyses and Dahlgren cells of fish, but it has also been identified in the brains
of lampreys and frog (Conlon et al. 1992). It has even been found in the spinal
cord of humans (Coulouarn et al. 1998).

3 Mechanisms of the Hormonal Regulation of Water and Salt

Across Epithelial Membranes

Neurohypophysial and adrenocortical hormones have special roles in regulating

water and salt transfer across epithelial membranes of tetrapod vertebrates. Such
effects are particularly important in the renal tubules and colon, and in the
Amphibia also occur in the skin and urinary bladder. The mechanism of action
of these hormones at such sites has attracted considerable interest. Special efforts
to understand their molecular nature have been fruitful. Studies on osmoregula-
tion in non-mammmals have played seminal roles in providing experimental
tissue preparations for these investigations.

3.1 Vasopressin and Vasotocin

Vasopressin and its homologue vasotocin have vital roles in limiting urinary
water loss in the kidneys of tetrapod vertebrates. An analogous effect also occurs
in the skin and urinary bladder of the amphibians. In mammals, this antidiuretic
response to vasopressin is principally due to the hormone's ability to increase the
permeability of the distal renal tubule-collecting duct system to water. A reab-
sorption of water occurs from the tubular fluid, down its osmotic gradient into
the renal medullary interstitium. This response, as described above, is initiated by
the interaction of vasopressin with V2-type receptors situated on the basolateral
borders of the renal tubular epithelial cells. An activation of the G-protein-linked
adenylate cyclase system follows resulting in the formation of cAMP. This
nucleotide then activates protein kinase A, which can phosphorylate proteins that
initiate the final response. Utilizing the same type of receptors, vasopressin can
also increase the permeability of the renal tubules to urea and promote the active
absorption of Na+. The latter two effects make a vital contribution to the ability
of the mammalian kidney to form hyperosmotic urine. In conjunction with the
countercurrent flow processes occurring in the loop of Henle and the vasae rectae,
they help establish, and maintain, a high osmotic concentration in the interstitial
fluids of the renal medulla and papilla. These three effects of vasopressin on water
and solute transfer are not confined to the mammalian kidney. They also occur
in response to vasotocin in non-mammalian tetrapods. Indeed, they were first
demonstrated (in vitro) in the skin of frogs (Fuhrman and Ussing 1951; Koefoed-
Johnsen and Ussing 1953). The urinary bladders of frogs and toads are similarly
responsive to neurohypophysial peptides.
Vasopressin (and vasotocin) can also contract vascular smooth muscle, an
observation that led initially to the naming of this hormone. This effect is medi-

78
ated by v,.-type receptors and is transduced by the phospholipase C phos-
phatidylinositol-DAG-IP3 system (see above). An activation of protein kinase C
results. In non-mammalian tetrapods, and possibly some fish, this vascular effect
may be elicited on the afferent glomerular arteriole and results in a decreased
GFR and even closure of glomeruli. Such a vascular effect contributes to the
observed antidiuretic effects of vasotocin in such species. In mammals, it has
been suggested that intrarenal vascular effects of vasopressin may influence
the pathways of renal blood flow (Cowley 2000}. Such an effect could contribute
to the maintenance of the high osmotic concentrations of fluid in the renal
medulla.
The mechanism of the actions of vasopressin and vasotocin on the perme-
ability of the renal tubule to water, urea and Na+ are of special interest (Fig. 2.11).
The first direct experimental studies utilized in vitro preparations of the skin and,
especially, the urinary bladders of frogs and toads. Vasopressin and related pep-
tides increase the permeability of such epithelial membranes to water, urea and
Na+, just as observed in mammalian kidney tubules. Water and urea move down
their concentration gradients only while an active transport of Na+ is promoted.
The kinetics of the process of the water movement suggested that vasopressin was
creating water-filled pores or channels in the membrane (Koefoed-Johnsen and
Ussing 1953). Unlike in the intestine, there was no direct linkage of the water
movement to Na+ transport. The presence of similar, but separate, pores was sug-
gested to account for the movement of urea. This effect of neurohypophysial hor-
mones on Na+ transport is mediated by activation and/or mobilization, probably
by phosphorylation via protein kinase A, of sodium channels in the apical plasma

Apical
plasma
membrane

J.."e~
'"'"""'
mobilization :!:.:,. ~
vestcle \0 /"~-~ Activation

Basolateral
plasma
membrane
I\. ~
t.:'.ll_
.-
ENaC
lnsertion1

~
PKC?

AQP2 -$·'
(mobilizatl\.,?)

Urea
transporter

Na• Water Urea AQP= aquaporln

PK= protein kinase

Fig. 2.11. Diagramatic summary of the various actions of neurohypophysial hormones (vaso-
pressin and vasotocin) on the permeability and transport of water, sodium and urea across
epithelial cells in the kidney tubules of tetrapods and the urinary bladder and skin of many
amphibians. For further information see the text. (After Ward eta!. 1999)

79
membrane of the cells. This response allows entry of Na+by diffusion into the cell.
It is then extruded across the basolateral cell membrane by the Na-K-ATPase
"pump" (Garty and Palmer 1997).
Chevalier et al. in 1974 (see also Chevalier et al. 1981) used an electron
microscopy freeze-etching technique to study the apical cell membrane of the frog
urinary bladder during exposure to oxytocin. (This neurohypophysial peptide is
a homologue of vasopressin and vasotocin.) Clusters of particles (intramembra-
nous aggregates) were observed within this membrane. They were found to be
associated with the stimulation of water transfer by the peptide. Similar obser-
vations were subsequently made on mammalian renal tubules exposed to vaso-
pressin. They resulted in the proposal of the particle "membrane shuttling"
hypothesis to account for the action of vasopressin on osmotic water transfer
(Wade et al. 1981). Thus, it was suggested that increases in permeability to water
in response to vasopressin resulted from the exocytotic insertion of water chan-
nels into the apical plasma membrane. These structures were mobilized from
cytoplasmic storage sites called aggrephores. The subsequent discovery of aqua-
porins provided a firm molecular basis for such a mechanism. In 1993, Fushima
and his associates cloned such a water channel from the rat renal collecting
duct. It has been named aquaporin 2 (AQP2). Aquaporin 2 contains two serine
residues, in human AQP2 Ser-256 and Ser-231, which can be phosphorylated,
respectively, by protein kinases A and C (Brown et al. 1998; Deen and Van Os 1998;
Borgnia et al. 1999; Ward et al. 1999; Christensen et al. 2000). This water channel
is stored in vesicles in the cytoplasm. Following cAMP-dependent activation
of protein kinase A by vasopressin, and the resulting phosphorylation of Ser-256
in AQP2, the storage vesicles are mobilized (see Fig. 2.11). They move along
the microtubules of the cell cytoskeleton towards the apical plasma membrane.
This process is referred to as vesicular trafficking. It appears to involve the
activity of the motor protein dynein (Marples et al. 1998). The vesicles then gain
access to the membrane in a process that appears to involve an interaction with
the F-actin filaments. This network lies beneath the plasma membrane. Exocy-
totic fusion with the plasma membrane then occurs which involves reactions
between the vesicular protein vAMP-2 and plasma membrane syntaxin-4. The
AQP2 is then inserted into the plasma membrane and provides channels for the
water transfer. The AQP2 can leave the membrane by endocytosis and is collected
in endosomes where it may possibly be reprocessed (Katsura et al. 1996). The
endocytosis of AQP2 may be initiated by phosphorylation of Ser-231 by protein
kinase C. A long-term regulation of the synthesis of AQP2 could involve activa-
tion of the cAMP response element (CRE) on the aquaporin gene (Marples et al.
1999).
Several urea transporters (UT-A1, UT-A2, UT-B1) have been identified that
contribute to the conservation of urea in the interstitial fluid of the renal medulla
(Bankir et al. 2000). The UT-A1 has been cloned and found to be present in the
apical plasma membrane of the renal inner medullary collecting ducts of
mammals (You et al. 1993; Nielsen et al. 1996). It facilitates the diffusion of urea
from the lumen of the tubule to the medullary interstitium. Its activity is regu-
lated by vasopressin. (The other urea transporters, UT-A2, which is present in the
thin descending loop of Henle, and UT-B1 in the vasae rectae, do not respond to

80
vasopressin.) The UT-A1 has been identified in cytoplasmic vesicles which, in
contrast to those containing AQP2, do not, apparently, undergo trafficking in
response to vasopressin (Inoue et al. 1999). The activity of UT-A1 appears to be
regulated in situ as a result of its phosphorylation by protein kinase A.

3.2 Mineralocorticoid Hormones

Aldosterone is the most active mineralocorticoid hormone in tetrapod verte-

brates. Its actions, as described above, usually commence with its binding to
mineralocorticoid receptors (MR) inside the cell. Cortisol and corticosterone
can also elicit mineralocorticoid-type effects but they are much less active than
aldosterone. However, their plasma concentrations are usually considerably
higher than those of aldosterone so that potentially they could elicit mineralo-
corticoid effects. Nevertheless, under normal physiological conditions their
access to MR is restricted by mechanisms that include their selective inactiva-
tion at potential target sites by the enzyme 11~-hydroxysteroid dehydrogenase
(11~-HSD) (Funder and Myles 1996). Most fish lack aldosterone but utilize corti-
sol to elicit both glucocorticoid and mineralocorticoid effects. They have a single
glucocorticoid-like receptor (see above).Glucocorticoid receptors can, on occa-
sion, apparently also mediate mineralocorticoid effects in tetrapods, as observed
in a cell line (A6) derived from the kidney tubules of the toad Xenopus laevis
(Watlington 1998).
The principal action of aldosterone is to promote the conservation of sodium
in the body fluids. This effect is mediated by its ability to increase active Na+ trans-
port across a variety of epithelial membranes, including the renal tubules and
colon of tetrapods. Aldosterone also stimulates the excretion of potassium, prin-
cipally by its secretion across the renal tubules and colon.
The process of transepithelial Na+ transport involves several events (Fig. 2.12).
They include entry of the ion into the cell through specific sodium channels
(ENaC) in the apical plasma membranes, followed by its extrusion across the
opposite, basolateral, surface of the cell as a result of the activity of Na-K-ATPase.
In 1961,Jean Crabbe found that aldosterone could stimulate such active Na+trans-
port, across the urinary bladder of the toad Bufo marinus under in vitro condi-
tions (Crabbe 1961a; Crabbe and De Weer 1964). This tissue preparation for many
years provided the principal information regarding the mechanism of action of
this hormone (Marver 1992). The response to aldosterone, unlike that to vaso-
pressin, was delayed for 60 to 90 min. It could be inhibited by the presence of
actinomycin D, which blocks genetic transcription, or puromycin, which blocks
the translation of mRNA. These early observations . were consistent with a
response that involved the synthesis of an essential protein, or proteins, that
mediate the response. Many subsequent studies, which have been extended to the
kidney and colon, have attempted to identify such proteins and find out what pre-
cisely they do. Substantial advances have been made, but the information is still
incomplete and consensus has not been reached. (Barbry and Hofman 1997; Garty
and Palmer 1997; Verrey 1999; Fig. 2.12).

81
Apical
plasma
membrane

Pleiotropic
response

3 Na•
Basal ~
plasma Na·K
membrane ATPase

Aldosterone @ 2 K•
MR = mineralocorticoid
receptor

Fig. 2.12. Diagramatic summary of the mechanism of action of aldosterone on Na+ and K+trans-
port across epithelial cells, such as in the kidney and colon of many tetrapods and the urinary
bladder of amphibians. The information has principally been derived from studies using the
mammalian and amphibian kidney, the mammalian colon and the amphibian bladder. (After
Verrey 1999 and references given in the text)

The entry of Na+ into many types of epithelial cells is now known to take place
through specific sodium channels (ENaC). This process can be rate-limiting for
such active Na+ transport. Careful kinetic studies, including the timing and mag-
nitude of changes in intracellular Na+concentrations, suggest that aldosterone can
increase the activity and possibly the numbers of ENaC. Increases in the passage
of Na+ through ENaC channels may be due to their activation so that their con-
ductance for Na+ increases. The possibility that they will be open could also be
enhanced. It is also considered likely that inactive sodium channels, which could
lie in reservoirs, such as cytoplasmic vesicles, may be inserted into the membrane.
New sodium channels may also be synthesized in response to aldosterone. The
ENaC channel consists of three subunits, a, Pandy. Activation of this ion channel
could involve phosphorylation of a site, or sites, by a kinase. Aldosterone has been
observed to promote serine I threonine phosphorylation of the p and y but not
the a subunits from such sodium channels prepared from the distal renal tubules
of dogs (Shimkets et al. 1998). It has also been suggested that activation of ENaC
channels could involve other processes, such as methylation, increased intracel-
lular pH or the action of Ca-calmodulin (Garty and Palmer 1997).
The presence of aldosterone has been shown to increase the transcription of
mRNA coding for various subunits of ENaC, but the results vary, depending on
the particular tissue studied and the species. In rat kidney, little effect was
observed, but in the colon there was an induction of the p andy subunits (Asher

82
 et al. 1996). In the rabbit kidney, aldosterone increased mRNA for they-subunit
(Denault et al. 1996). In the distal colon of rats, aldosterone increases the tran-
scription of the 13 andy subunits of the ENaC channels (Epple et al. 2000). The
colon of chickens on a low-sodium diet, when plasma aldosterone levels are
elevated, exhibits a marked increase in mRNAs for the a and 13 subunits
(Goldstein et al. 1997). While the principal effects of aldosterone on the renal
tubule appear to occur in the medullary collecting duct, a response has also been
observed in the distal convoluted tubule. The entry of Na+ across the apical side
of the epithelial cells in this tubule is mediated by the Na-Cl cotransporter protein.
The expression of this protein was increased nearly fourfold by aldosterone (Kim
et al. 1998).
The successful transit of Na+ out of epithelial cells depends on the activity of
Na-K-ATPase on their basolateral surfaces. This enzyme can be activated by the
increase in intracellular Na+ that occurs following its entry into the cell. However,
when exposure to aldosterone is prolonged for about 5 h or more, there is also an
increased synthesis of this enzyme. Such an effect on Na-K-ATPase was first
clearly shown in the toad urinary bladder by Geering and his collaborators ( 1982 ).
This transport enzyme contains two major subunits, a and 13. In cultured A6
kidney cells from the toad Xenopus laevis, aldosterone has been found to induce
a two- to fourfold increase in the synthesis of both of these subunits (Verrey et
al. 1987). Similar effects have also been observed in mammalian kidneys and
colon (Ewart and Klip 1995).
The action of aldosterone has been assumed to commence with the activation
of an early-response gene, resulting in the initiation of a signal-transducing
cascade and the induction of a protein or proteins that contribute the final effect.
The response appears to be pleiotropic and could involve the formation of further
transcription factors. It has been difficult to identify such components from
among the many mRNAs and proteins that are produced in the target cells. Several
candidates have been investigated. The Ras proteins are small G-proteins that are
expressed by the Ras gene family. They are involved in many signal-transduction
pathways, especially those involved in mitogenic responses. Aldosterone has been
observed to increase the expression of K-Ras2 in A6 cells from the kidney of
Xenopus laevis (Spindler and Verrey 1999). It has also been observed to increase
the methylation of Ras (Al-Baldawi et al. 2000). Inhibition of such methylation
inhibits the response to aldosterone. Apart from inducing the expression of K-
Ras2, aldosterone could also be inducing modulatory proteins that activate an
essential methyltransferase enzyme. When K-Ras2 and ENaC channels are coex-
pressed in Xenopus oocytes, Na+ transport through the ion channels is increased
(Mastroberardino et al. 1998). The Ras protein may be playing an integrative role
in the aldosterone-signalling pathway. However, a more primary signal would
appear to be occurring more upstream in the process. Such a candidate is the gene
sgk, which was first identified from a rat mammary gland tumour cell line
(Webster et al. 1993). Its product is a serine I threonine kinase which can be
induced by aldosterone in Xenopus kidney A6 cells, the renal collecting duct of
rabbits and the colon of rats (Chen et al. 1999; Naray-Fejes-Toth et al. 1999;
Shigaev et al. 2000). When the sgk protein from the A6 cells is coexpressed with
ENaC channels in Xenopus oocytes, Na+transport is increased. The activity of the

83
sgk protein is dependent on the presence of a lipid kinase, phosphatidylinositol3-
kinase (P13K) (Kobayashi and Cohen 1999; Wang et al. 2001). The latter's activ-
ity can be increased by insulin. This effect may account for the syngergism that
has been observed between the actions of aldosterone and insulin (Andre and
Crabbe 1966; Wang et al. 2001).
The regulatory effects of aldosterone in promoting potassium excretion have
been observed in the mammalian renal tubule and colon. It is not seen in the
amphibian urinary bladder, possibly reflecting a deficiency of potassium chan-
nels in the epithelial apical plasma membrane. Such potassium channels are
present in this membrane in the mammalian epithelia, and aldosterone appears
to promote a secretion of K+ through them (Giebisch 1998). Two indirect mech-
anisms exist for a secretion of K+ and may contribute to aldosterone-stimulated
K+ transport. An increase in the activity of Na-K-ATPase could produce a higher
intracellular concentration of K+, thus facilitating its diffusion out of the cell.
Concomitantly, the increase in uptake of Na+ across the apical plasma membrane
appears to result in its partial depolarization. This change in electrical potential
would also be expected to favour the diffusion of K+ out through the potassium
channels. However, aldosterone may have a more direct effect, as it has been
observed to increase the transcription of mRNA coding for ROMK potassium
channels in the plasma membrane of rat distal renal tubules (Beesley et al. 1998).

84
Chapter 3

The Mammals

1 General Introduction

About 1050 contemporary genera of mammals are named by Walker (1964) in

his monograph Mammals of the World. Three of these belong to the order
Monotremata (egg-laying mammals), 90 to the order Marsupialia (typically unde-
veloped young kept in pouches), and the remainder are eutherians (placentals).
Monotremes are known only from the Australian region and are represented by
the echidna and platypus. This order probably represents a separate line of mam-
malian evolution, beginning in the Triassic period. The marsupials and placen-
tals probably diverged from a common stock early in the Cretaceous period, about
85 million years ago. The Australian (75 genera) and American (15 genera) mar-
supials subsequently diverged late in the Cretaceous. The placental mammals
today contain about 950 genera, of which 360 are rodents (Rodentia) and 180 are
bats (Chiroptera). The other generically numerous groups are the Insectivora
(hedgehogs, shrews), 66 genera; Primates (man and monkeys) 62; Cetacea
(whales) 35; Carnivora 103; Pinnipedia (seals) 20 and Artiodactlya (pigs, camels
cattle, sheep) 82. The mammals have a wide geographic and osmotic distribution;
they are predominantly terrestrial and are even found in the driest desert regions,
though some are aquatic and live in rivers and lakes or in the sea. Only one genus
of the monotremes (Ornithorhynchus, the platypus), and one marsupial (the
South American water opossum, Chironectes) live in fresh water, and these groups
have no marine representatives. Most mammalian orders have representatives
that live in desert regions.
The ability to osmoregulate in such contrasting environments depends on
physiological and behavioural adaptations, many of which are uniquely suited to
the particular needs of mammals. In the absence of such specializations most
temperate terrestrial species find it difficult to survive in areas where water is
more restricted, though there are some exceptions such as the dog and European
rabbit, which thrive in the desert conditions of Australia. Dispersal of mammals
is, nevertheless, relatively restricted by deserts, and especially limited by salt-
water barriers (Darlington 1957). Bats, due largely to their aerial capabilities, have
the widest distribution among the mammals, reaching isolated oceanic islands,
such as the Azores, New Zealand and Hawaii, that are otherwise inaccessable
to all but marine species. The rodents also have often managed to cross salt-
water barriers (probably on rafts), but if the aid of man can be excluded, this prob-
ably occurs only across the short distances to islands lying adjacent to the con-
tinents. Such journeys, whether as aviators or mariners, nevertheless constitute

85
an osmoregulatory feat of some substantial magnitude considering the rather
unfavourable conditions experienced by terrestrial mammals in oceanic regions.

2 Osmoregulation
Two evolutionary events have had profound effects on the osmoregulatory prob-
lems of tetrapods. The first was the adoption of a terrestrial, instead of an aquatic,
habitat. Evaporation of water then made its initial appearance as a vertebrate
problem. In addition, there arose the novel necessity to replenish the body water
periodically from the sporadic sources available in a terrestrial environment.
The second major event to influence tetrapod water metabolism was the adoption
of homoiothermy by the birds and mammals (or possibly an ancestor of these).
Potential evaporation from the body surface is increased at the relatively high, and
sustained, body temperatures of such animals, while the added metabolic need for
respiratory gas exchanges also increases evaporative water loss from the respira-
tory tract. Heat loss accompanying evaporation of water is utilized for cooling in
hot environmental conditions, when additional evaporation is facilitated by the
secretion of sweat or by panting. Viviparity also increases the needs for water and
salts, especially in placental mammals, which retain the young in utero until they
are relatively well developed. The secretion of milk to nourish the young places
yet another periodic osmoregulatory burden on the mother, but has obvious
advantages for the offspring. The mammals thus have the usual tetrapod problems
with respect to their water and salt metabolism, and a few additional ones as part
of the price that they must pay for their unique physiology. However, the high
metabolic rate of mammals allows them to travel considerable distances for food
and water, while their viviparity and ability to suckle their young foster reproduc-
tion in situations in which it could otherwise be difficult, both nutritionally and
osmotically. It should be remembered that while the high rate of metabolism in
mammals increases their requirements for osmoregulation, such adjustments may
be facilitated by the increased energy produced by the cells of such animals.
The relative abundance or scarcity of salts may limit the distribution of
mammals. An excess of water or salts in the food can be tolerated by some species,
but not others. Marine mammals like whales and seals live in a hyperosmotic salt
solution, equivalent in concentration to 3.3% sodium chloride. Many marine
mammals eat invertebrates that are isosmotic to sea-water. Such mammals do not
appear to drink sea-water normally but, when feeding on invertebrates, take in
large quantities of salts, far more than most other mammals could tolerate with
the limited quantities of osmotically-free water that are available. Most terrestrial
mammals cannot survive if provided with drinking water that contains 2 to 3%
sodium chloride, but there are exceptions. The North African sand rat, Psam-
momys obesus, normally eats halophytic plants with a salt concentration higher
than that of sea-water (Schmidt-Nielsen 1964a), while the western harvest mouse,
Reithrodontomys r. halicoetes, of the United States eats similar plants and can
drink sea-water (Haines 1964). Other species may drink sea-water sporadically,
and this has been shown among the Australian marsupials,including the Tammar

86
wallaby, Macropus eugenii (Kinnear et al. 1968). In many areas of the world there
is a deficiency of sodium in the soil, a condition that appears most often in the
interior of continental areas and high mountainous regions. The vegetation
reflects the low sodium content of the soil, so that herbivorous animals may have
restricted amounts of salt available. Thus, the herbage in grazing areas of central
Australia may contain only 1 to 3 mEq. kg- 1 dry weight of sodium, compared to
100 to 350mEq.kg- 1 dry weight in coastal areas (Denton 1965, 1982). The popu-
larity of "salt licks" among mammals in such regions is well known.

2.1 Water Loss

2.7.1 Cutaneous

Cutaneous water loss takes place through the skin by diffusion, and as a result of
secretion by the sweat glands. This water is evaporated from the body surface,
resulting in a loss of heat, a process that can be used physiologically for cooling
in hot environments. In some species, including humans, cattle, camels and some
antelope, sweating is the principal mechanism for thermal cooling. However, in
other mammals, such as horses, dogs and small herbivores, it is generally utilized
only during exercise. Evaporation from the respiratory tract by panting is other-
wise the predominant cooling mechanism (see below). Sweating is considered to
be a relatively inefficient way of cooling, as in some mammals, such as horses, it
mainly occurs from the surface of the fur. When it does take place directly from
the skin the surface temperature declines and facilitates further gain of heat by
conduction from the environment. In man, the eccrine sweat glands are usually
considered to be associated principally with thermal cooling while the apocrine
glands, which are associated with hair follicles, respond to other stimuli. Sweat-
ing is initiated by exercise in the horse, a response that is stimulated by elevated
levels of adrenaline in the blood and one which contributes to heat and water
losses (Lovatt Evans et al. 1956). The sweat glands can secrete large volumes of
fluid; a man working in the desert loses up to 151 of water a day in this manner.
Sweat glands are typically mammalian structures though their presence, and
relative importance for thermal cooling is not the same in all species. MacFarlane
(1964) found that the maximal rate of thermal sweating in merino sheep was
32gm-2 h- 1, while the camel can form 260gm- 2 h-1 (Schmidt-Nielsen et al. 1957).
Many mammals, such as the rabbit and rat, do not possess sweat glands, though
water loss can still take place across the skin. Dehydration may result in a
decreased rate of sweating. The camel after 24 h without water perspires at 60 to
70% of the rate seen when it is normally hydrated (Schmidt-Nielsen et al. 1957).
Thermal cooling responses of sweat glands are under the control of the sympa-
thetic nervous system. In man, the final transmitter is acetylcholine. However, in
bovidae, like domestic ox and various wild species like the oryx, eland, wildebeest
and buffalo which live in East Africa, these nerves are adrenergic (Findlay and
Robertshaw 1965; Robertshaw and Taylor 1969). The injection of adrenaline in
these species as well as in the horse, sheep and camel results in the secretion of

87
sweat. This type of response may arise physiologically during exercise rather than
in response to heat stress. Noradrenaline is relatively ineffective. Thermal sweat-
ing is abolished in the dehydrated oryx, though sweat glands can still respond to
injected adrenaline (Taylor 1969). Kangaroos utilize sweating as a cooling mech-
anism during exercise (Dawson 1973; Dawson et al. 1974). As soon as the activity
stops, the sweating ceases and the animals continue to pant in order to cool. The
sweat glands, like those in other mammals, have an adrenergic innervation. The
injection of adrenaline also results in sweating, but such a physiological role for
this hormone has not been established. It seems likely that reductions in the
volume of sweat secretion during dehydration are mediated by nervous, rather
than endocrine, mechanisms, but changes in the level of circulating adrenal
medullary hormones possibly could have an effect in some species.

2.1.2 Respiratory

The respiratory tract is a major route of water loss in tetrapods and more espe-
cially in the mammals and birds. This loss takes place by evaporation, as an
unavoidable consequence of the uptake of oxygen and excretion of carbon
dioxide, but this avenue can also be utilized physiologically for thermal cooling
by panting. The normal overall obligatory losses of water from the respiratory
tract increase or decrease with parallel changes in metabolic rate and oxygen con-
sumption. Normally, mammals extract about 30% of the oxygen present in the
inspired air, but in certain circumstances this may be altered, with reflected
changes in the accompanying water loss. Dick (C. R.) Taylor (1969) showed that
an African antelope, the oryx, which lives in desert areas, may reduce its oxygen
consumption by 30% when it is dehydrated, and, by breathing more deeply, can
extract additional oxygen from the inspired air. The net result is a considerable
reduction in water loss. Similarly, Schmidt-Nielsen and his collaborators (1967)
have shown that the camel reduces its oxygen consumption when dehydrated.
Such a decrease in metabolism is not invariably seen in dehydrated mammals.
Thus, the East African waterbuck, Kobus defassa ugandae, fails to change its rate
of oxygen consumption when deprived of water (Taylor et al. 1969). Largely as a
result of the high rate of accompanying evaporative water loss, these antelope
withstand water deprivation poorly, even when compared with domestic Here-
ford cattle. It seems possible that the ability to reduce the metabolic rate under
such conditions constitutes a physiological reaction that could adapt the animals
more readily to the changed circumstances. The thyroid gland influences the
metabolic rate in mammals, but it is not known whether it is concerned with the
changes that are observed in dehydrated animals. Such a possibility should be
simple to test.

2.1.3 Renal Water Loss

Obligatory losses of water occur in the urine in response to the homeostatic need
to excrete solutes that are either obtained from the diet or are formed as a result
of metabolism. In mammals, the principal product of the latter process is urea.

88
 In many herbivores, including cattle, sheep and kangaroos, the fermentative
microorganisms in their guts can reutilize this urea to make proteins (Stevens and
Hume 1995). Such urea recycling may increase under conditions of water restric-
tion and a low protein diet. The urea enters the gut in the saliva and by diffusion
across its lining mucosa. The necessity to excrete urea in the urine can thus be
reduced in such mammals. The magnitude of water loss in the urine of mammals
depends, apart from excesses of dietary salt and urea, on their ability to concen-
trate the urine. The proportion of the total water loss each day varies in different
mammals and reflects the environmental conditions, which usually determine the
extrarenal losses. In normal circumstances renal water excretion is less than 50%
of the total water loss, but it may be less than 10% under hot dry conditions when
evaporative losses are increased.
The mammalian kidney, like that of birds and reptiles, is a metanephric one
(Braun and Dantzler 1997). However, unlike in the other phyletic groups, it lacks
a renal portal blood system. The nephrons of mammals are generally larger than
those in most other species. The mammalian kidney can secrete urine that has a
concentration that is hyperosmotic to the plasma. Among vertebrates, the birds
are the only other species that have such an ability, but they generally cannot con-
centrate their urine as highly as mammals do (Table 1.6). Nevertheless, the capac-
ity to concentrate the urine is quite variable in different species of mammals. Thus,
mountain beaver can only secrete urine with a maximum concentration of about
500 mosmoll- 1 while in Australian hopping mice it can exceed 9000 mosmoll- 1•
The ability to form hyperosmotic urine is related to the structural arrange-
ment of the nephron which includes the renal tubular loop of Henle. The latter is
present only in mammals and birds. The renal capillaries also form long loops,
which descend into the renal medulla (vasae rectae). The renal tubules and the
vasae rectae form, respectively, a countercurrent multiplier system and a coun-
tercurrent exchanger for solutes. These morphological arrangements contribute
the mechanisms necessary for the formation of hyperosmotic urine. In 1944,
Sperber observed that the length of the loop of Henle in different mammals, as
reflected by the thickness of the inner renal medulla, could often be correlated
with their ability to concentrate the urine. This ability also appeared to be related
to the degree of aridity of their normal habitats. Such correlations have often been
observed, but there are a number of exceptions (Greenwald 1989; Beuchat 1996).
The "metabolic intensity", or "capacity", of the renal tissue also appears to be an
important non-morphological factor that can contribute to an ability to concen-
trate the urine. The weight of the kidney in mammals increases with their body
weight and generally reflects an increase in the numbers of nephrons. This
increase in kidney size usually follows a predictable formula. However, it is espe-
cially interesting to observe that marine mammals, including whales, dolphins
and seals, have exceptionally large kidneys (Beuchat 1996). Nevertheless, their
urine-concentrating ability is unremarkable compared to many other mammals.
In mammals, an absence of vasopressin or an inability of the distal renal
tubule-collecting duct system to respond to this hormone results in the forma-
tion of large volumes of dilute urine (the disease called diabetes insipidus). This
condition is mainly due to a decreased reabsorption of water from the distal renal
tubular system. As described in Chapter 1, vasopressin, by promoting the reab-

89
sorption of urea and sodium from the renal tubules, also helps to maintain the
renal medullary osmotic concentration gradient that is necessary for the forma-
tion of a hyperosmotic urine. It could also be contributing in this way to the urea-
recycling mechanism in some herbivorous mammals.

2.1.4 Faecal Water Loss

Water loss in the faeces depends on their water content and the total mass of faeces
that are formed (Degen 1997}. Rodents absorb about 90% of the content of a diet
of seeds, and carnivores appear to exhibit a similar efficiency in the utilization of
their food. However, most herbivores utilize only about 65 to 70% of their fibrous
diet of grasses and shrubs. Faeces usually contain 60 to 70% water. However,
depending on the species, this concentration can often be reduced when water is
not freely available. The faeces of camels normally contain about 55% water, but
after a day without drinking the water content decreases to about 45% (Schmidt-
Nielsen 1964a). The faecal water content of jackrabbits living in the Mohave
Desert can be as low as 38% while that of wild rabbits is about 48%. Several species
of rodents, especially those living in arid areas, can form faeces containing about
40% water. In sheep, the water content of the faeces varies from 75 to 45%.
However, cattle cannot reduce the water content of their faeces as efficiently
(McKie et al. 1991}. Water is mainly removed from the faeces in the descending
(distal) colon. In sheep, the mucosal epithelium lining the colon is considered to
be "tight", with narrow paracellular pathways. In cattle these intercellular path-
ways are described as being "leaky", which may contribute to their inability to
achieve high levels of faecal dehydration. It appears that the reabsorption of salt
from the colon is more effective in cattle than in sheep, but the higher osmotic
concentration of gradients necessary for the formation of drier faeces cannot be
maintained. The mechanism that is utilized to dehydrate the faeces in rats has
been described in Chapter 1. In rats, the establishment of the osmotic gradients
involved in maintaining the necessary suction tension and fluid absorption across
the distal colonic crypt barriers is increased by aldosterone (Naftalin and Pedley
1999). Mammals that form dry faeces have been observed to have a longer distal
colon than those that excrete wetter faeces. This relationship has been observed
in East African antelopes, rodents and kangaroos (Osawa and Woodall 1992;
Woodall and Skinner 1993; Murray et al. 1995).

2.1.5 Water Loss Associated with Reproduction

Reproduction results in increases in the need for water (and salt) in mammals.
This additional requirement reflects pregnancy and the growth of the foetus and,
subsequently, lactation. Mammals that live in regions of seasonal aridity may
synchronize their breeding seasons to coincide with the availability of adequate
drinking water and food. However, an unexpected subsequent drought can result
in the loss of the young. Kangaroo rats living in the Mohave Desert can normally
survive without drinking on a diet of dry seeds. However, during periods of repro-
duction they may seek more succulent vegetation (Nagy and Gruchacz 1994). The

90
milk of desert species often contains high concentrations of fat and less water
than in species from more temperate regions. Arecycling of water from the young
to the mother, and sometimes even the father, can result from anogenitallicking
(Degen 1997). This retrieval of water from the urine and faeces has been studied
most often in rodents but also occurs in other species, including the young in the
pouch of marsupials (Dove et al. 1989). It has been calculated that during early
lactation in rats up to 70% of water in the milk is recovered in this way. The urine
of young mammals is much more dilute than in the adults and they are relatively
unresponsive to vasopressin. The adult kidney with its greater concentrating
ability thus provides a more efficient organ for conserving water under such con-
ditions. In mammals living in areas where there is deficiency of salt in the diet,
such a mechanism could also be useful for the conservation of sodium.

2.2 Salt Loss

2.2.1 The Sweat Glands

The secretion of the sweat glands contains dissolved solutes, principally sodium,
potassium, chloride and bicarbonate. In mammals that utilize sweat secretion for
thermal cooling the losses of these solutes, especially sodium, may be consider-
able. The sodium concentration of sweat in humans varies from 5 to 60 mEq 1- 1,
being greatest when the rate of sweat secretion is high (Thaysen 1960}. During
sodium depletion the amount of this solute in the sweat decreases more than five
fold, while the potassium level rises. Such changes require several days to occur.
Schmidt-Nielsen (1964a) suggested that in herbivorous animals, like the donkey,
little sodium is lost in sweat, and measurements by MacFarlane (1964) on sheep
and camels support this view. The sweat of the camel contains 9.5 mEq l- 1 sodium
and 40 mEq l- 1 potassium. In humans, a decrease in the Na/K ratio in sweat has
been related to the action of the adrenocortical hormones (Conn et al. 1947}, and
it seems likely that these steroids may contribute to the acclimatization in the salt
levels of the sweat that is seen in other species.

2.2.2 The Gut

The gut is an avenue of entrance and exit of salts from the external environment.
Salts are taken into the gut with the food and water, while large volumes of fluids,
rich in electrolytes, are continually secreted into the lumen of the alimentary
tract in order to facilitate digestion. These fluids include saliva, various gastric
and intestinal secretions, the bile and the pancreatic juices. In order to maintain
adequate salts in the body, all of the electrolytes must ultimately be reabsorbed.
Inadequate intestinal absorption, which may occur, for instance, as a result of
infection, can result in death from water and electrolyte deficiency.
The composition of the secretions derived from the different salivary glands
varies, and depends on the species and the physiological condition of the animal.
Salivary secretion in the sheep has been extensively studied by Denton and his

91
 20 180 (m equiv.)
r x A'v~
1/ '. . . ,
~--X'I:;:o, , X I ;.:, 80

X
Parotid 10 160 Parotid x~·-o~x ......•-.-•-• ,x o•""'Pl
salivary "' I I (mequiv./ l) 60
salivary 140 '\ ~l'/ 0 Parotid
4 sodium ~ saliv.ary
40
Na./K• 120 concent. ;\ ,/ potass1um
2 x- -x 6 , , 0/ C9._ncen1.
ratio ._.--.t" \~o-~o-.x·-Rr '..._.___ 20
o -o 100 'x ' ', , / -

(ml. m1n) 1 x ----------------------~0

~~~~--------------------------
Parot1d
salivary
secretion 0

I. V. lnfusion
Aloosterone dl
10 ~ g/ hr d. Isomer
11J-g/hr d. Isomer

2 4 6 8 10 12 14
Hours
Fig. 3.1. Sheep Zachary (adrenally insufficient, Na+ deficit 250 mEq.). Effect of intravenous
infusion of aldosterone on parotid salivary Na+ concentration x---x; K+ concentration - • ;
and parotid salivary Na+: K+ o-o. Parotid secretion rate is also shown. (Blair-West eta!. 1967)

collaborators (Blair West et al. 1967). The total volume secreted by this species in
a day is 6 to 161, principally by the parotid glands. Normally, in a sheep, with ade-
quate dietary sodium, the parotid secretion contains 180 mEq sodium l-1 and
5 mEq. potassium 1- 1 (Na/K is 36). If sheep are deficient in sodium, the levels can
change to give a Na/K ratio of 10/170mEql-l, or 0.06. Adrenalectomized animals
exhibit little adjustment in their response to sodium depletion. The infusion of
aldosterone can, however, restore this deficiency (Fig. 3.1).
The rate of secretion of aldosterone from the adrenal cortex can increase 13-
fold in sheep depleted of 300 to 500 mEq of sodium, and the levels of this steroid
are consistent with the amounts which must be infused in order to change simi-
larly the composition of the saliva. Cortisol and corticosterone can also alter the
electrolyte level in the saliva, but the necessary concentrations are large, and prob-
ably only of pharmacological significance. Vasopressin has no effect on salivary
secretion.
The site(s) of action of the corticosteroids on the salivary glands is uncertain;
they conceivably could act on the primary secretory mechanism in the acinar
cells, or alter reabsorption from the ducts. Blair West et al. (1967) suggest that
aldosterone probably acts at both sites.
The biological importance of the action of aldosterone on the electrolyte com-
position of saliva is more readily apparent in animals that secrete large volumes
of saliva. These include many of the Artiodactyla, which digest their herbivorous
diet with the aid of microbial fermentation. The volume of the fluid in the diges-
tive tract of these animals is largely derived from the salivary glands, making up

92
 10 to 15% of the body weight, and containing sodium equivalent to half that
present in the extracellular fluid. A physiological mechanism to limit such seques-
tration of sodium could well be vital for survival when the amounts of this ion
in the body are depleted, and its dietary availability is limited. In addition, some
mammals drool saliva from the mouth when the rectal temperature is elevated
in hot situations. Such salivation has been observed in several marsupials and
placentals, including some rodents, rabbits, cats and cattle. If this saliva is spread
over the fur it may aid in cooling. In rodents a substantial loss of fluid may occur
in this way (Degen 1997). The forearms of kangaroos have a plentiful blood supply
and they spread saliva over this area when environmental temperatures are high
(McCarron and Dawson 1989). This response does not occur when the kangaroos
are dehydrated. The use of saliva for evaporative cooling may constitute an emer-
gency reaction that could be life-saving, but its efficiency is uncertain (Schmidt-
Nielsen 1964a). The accompanying loss of salts in the saliva possibly could be
reduced by aldosterone, as observed in the saliva of sheep (Fig 3.1).
The absorption of salts from the diet and the secretion that occurs into the
gut takes place continually in the small intestine. A role for hormones in the
processes of such conservation is not readily apparent. However, an increased
secretion of cr- into the intestine can be promoted by guanylins that are secreted
by enterochromaffin cells in the lining mucosa (Forte et al. 2000). A hormonal
role for these peptides is considered likely but is not established. However, in
conjunction with their diuretic and natriuretic actions on the kidney they could
be contributing to a postprandial excretion of excess salt (Fig. 3.2). The colon
is the site of a hormonal mechanism for the fine-tuning of sodium and potassium
excretion in the faeces. Such a role for adrenocorticosteroids had long been
suspected as a result of changes in the salt concentrations of the faeces that
accompanied human Addison's disease. This condition results from a destruction
of the adrenal cortex. In 1965, Cofre and Crabbe demonstrated that aldosterone
had a direct effect in vitro, in promoting Na+ absorption from the colon of the
toad Bufo marinus. Such an effect was also demonstrated in vivo in humans and
rats, where it is usually accompanied by an increased excretion of K+ in the faeces
(Levitan and Ingelfinger 1965: Edmonds and Marriott 1970; Binder and Sandie
1994).

2.2.3 The Kidney

Large volumes of plasma are filtered across the glomerulus; this ultrafiltrate
passes into the renal tubule, where most of its constituents are reabsorbed. The
quantities of solutes filtered are enormous, and usually more than 99.9% of the
sodium is reabsorbed back into the plasma. These processes are relatively greater
in mammals than in cold-blooded species. If the diet contains an excess of
sodium, more sodium will be excreted. Most vertebrates can form a hyposmotic
urine which may contains only small amounts of sodium. In animals on a normal
diet such urinary losses are easily replenished, but in some circumstances even
these may be physiologically significant. The formation of large volumes of urine,
due to excessive drinking, or to feeding on a very succulent diet, exaggerates such

93
 8
Postprandial response to gain of salt In meal ?

mu~~!sl cells
J,

I
{!
Guanylln Natriuretic peptldes

Aldost_erone ~luroguanylln \ ANP, BNP

Inhibits
aldosterone
secret1on? secretion
Inhibits?

Intestinal ~
Kidney
mucosa Na-appetlte guanylate
guanylate (Brain)
cyclase cyclase
-!,
cGMP cG~P
ct· i J,
Natriuresis
Secretion
HCO;

Fig. 3.2. A suggested model for the endocrine control of salt excretion following feeding in
mammals. (After Forte et a!. 2000, with some additions)

losses. The role of the adrenal cortex in renal sodium conservation and potassium
excretion has already been described (Chap. 2); aldosterone promotes reabsorp-
tion of sodium and secretion of potassium across the wall of the distal renal
tubule and collecting ducts. The absence of a functional adrenal cortex results in
an excess loss of sodium in the urine and failure to excrete adequate potassium.
Changes in the sodium content of the diet are reflected in the sodium content of
the urine, and the circulating levels of the adrenocortical hormones, especially
aldosterone. Thus, rabbits living in the sodium-poor areas of the plateau of the
Australian Snowy Mountains have urinary sodium levels as little as one-thirtieth
of those rabbits living in adjacent sodium-replete grasslands (Blair West et al.
1968). The adrenal glands of the sodium-deficient rabbits are enlarged and the
levels of aldosterone and renin in the blood are three to six fold greater than in
the sodium-replete animals.

2.3 Accumulation of Water and Salts

Water and salts are obtained:

1. In the food. The water content of plants is often equivalent to more than
95% of their weight, and a carnivorous diet contains about 70% water. Even dry
seeds contain water that is taken up hygroscopically from humid air. In addition
to such directly available fluid, the metabolism of fats, carbohydrates and proteins
results in formation of additional water; the yield from oxidation of 1 g of fat is
1.1 ml, while the same amount of carbohydrate gives 0.6 ml and protein 0.4 ml.
There has been much conjecture about the importance of fat reserves in assist-

94
ing animals to maintain a positive water balance. The camel's hump was proba-
bly the earliest recipient of such speculation, but this has been discounted by Knut
Schmidt-Nielsen. It must be remembered that the oxidation of an energy sub-
strate requires an exchange of gases in the respiratory tract, and this may result
in evaporative water loss. If the animals are breathing dry air, oxidation of such
substrates will result in a net loss of water, due to saturation of the expired air
with water vapour. Inspiration of more humid air will decrease this loss, so that
in marine mammals like the whale, which breathe air already saturated with water
vapour, a net gain of water from metabolism can be expected.
As already described, the sodium content of plants may vary considerably and
in some inland continental and alpine regions the sodium levels may be low. This
is the prime determinant of the salt status of all herbivorous animals living in the
area, while carnivorous species obtain adequate sodium from the prey on which
they feed. The diet of some mammals may consist predominantly of halophytic
plants with a high concentration of salts such as eaten by African sand rats
(Schmidt-Nielsen 1964a), possibly Australian hopping mice (MacMillen and
Lee 1969) and kangaroos and sheep living in the Australian outback (Dawson
et al. 1975).
Many mammals, especially herbivores, that live in inland areas of the world
where the vegetation has a low concentration of sodium, actively seek, and regu-
larly visit, mineral deposits containing sodium chloride (Denton 1982). They
replenish their depleted body sodium at such sites, which are called salt licks. This
behaviour has been observed more often during pregnancy and lactation, when
it may involve a response to reproductive hormones. Humans living in such
regions may also be affected and often place a high commercial and monetary
value on salt.
2. In the drinking water. Drinking supplies the water requirement beyond
that obtained from the food. O'Connor and Potts (1969) have emphasized the pre-
dominant importance of this process in regulation of a positive water balance.
The urinary volume and concentration of dogs on a standard diet, in contrast to
what they drink, does not vary over a wide range of environmental circumstances.
This suggests that it is drinking, rather than kidney function, that is responsible
for regulating the positive water balance. Fresh water, containing little dissolved
salt, is usually the beverage of choice. However, in some situations the only drink-
ing water that is available may contain significant quantities of salt that are ap-
parent on tasting (brackish water). Such water supplies are regularly utilized and
can help sustain animals providing that the sodium chloride concentration does
not exceed the capacity of the kidney to concentrate the salt in the urine. In some
unusual circumstances animals may even drink sea-water (= 3.3% NaCl).
However, in most instances when this occurs, diuresis and diarrhoea follow,
resulting in further dehydration.
The sensation of thirst, which results in drinking, and an appetite for sodium
are initiated in the brain, especially in regions near the base of the third ventri-
cle and the hypothalamus (Fitzsimons 1998). Thirst is a complex process that can
be initiated by increases in the concentration and decreases in the volume of the
extracellular fluid. The administration of angiotensin II, into either the brain or
the peripheral circulation, can evoke drinking behaviour in many vertebrates,

95
including mammals. Extracellular hypovolemia initiates activation of the renin-
angiotensin system. The angiotensin II that is formed in the plasma contributes
to the thirst-drinking mechanism. It activates AT 1 receptors in regions of the
brain, including the subfornical organ and the organum vasculosum of the lam-
ina terminalis. These sites are accessible to the peripheral circulation. Natriuretic
peptides also have receptors in such tissues and can antagonize this effect of
angiotensin II.
Angiotensin II can also induce sodium appetite (Weisinger et al. 1987}.
However, this effect is slower and it is delayed in onset compared to the drinking
response. Sodium appetite is mediated through a "sodium-appetite centre" that
lies near, but is separated from, the thirst centre (Weisinger et al.1993}. This effect
on sodium appetite has been observed in rats, mice, sheep, wild rabbits, cattle and
pigeons. Sodium appetite can also be promoted by the administration of ACTH
(Weisinger et al. 1980}. Its principal effect appears to be mediated by adrenocor-
tical steroids, including aldosterone. Angiotensin II and the adrenocorticosteroids
may have synergistic effects on sodium appetite. A release of ACTH in response
to stress in mice has been shown to evoke sodium appetite (Denton et al. 1999).

2.4 Effects of Dehydration on the Body Fluids

The water content of terrestrial species of mammals is usually about 70% of their
body weight. However, there is a range between 60 and 70% (Degen 1997}. The
differences reflect such factors as the fat content, the season and the volume of
fluids that are sequestered in the gut. The latter may be substantial in herbivo-
rous animals when the rumen, caecum and large intestine can provide capacious
chambers for microbial fermentation (Stevens and Hume 1995}. This gastroin-
testinal solution is considered to be part of the interstitial fluid compartment. The
blood plasma in mammals is usually about 5% of the body weight and its volume
is maintained within the vascular space by the interactions of the capillaries, the
osmotic pressure of the plasma proteins and the hydrostatic pressure provided
by the beating heart (see Chap 1). An excessive loss of water from the plasma
results in an increased viscosity of the blood, which hampers its circulation
(Horowitz and Samueloff 1988}. This effect can retard the loss of body heat, espe-
cially in hot external environments, and can result in fatal increases in body tem-
perature (heat stroke). Some species, especially those adapted to life in desert
conditions, can maintain their plasma volume during periods of dehydration
(Schmidt-Nielsen 1964a; Horowitz and Borut 1970; Degen 1997}. Such plasma
volume conservers include camels, the burro, kangaroos and some antelope and
rodents. Species that do not conserve their plasma volume under such conditions
include humans, dogs, merino sheep and laboratory rats. Species that conserve
their plasma volume during dehydration may initially lose more water from the
interstitial and intracellular fluids than from the blood plasma, and this can help
maintain the blood circulation. This response can be influenced by the degree and
speed of dehydration. It appears to be related to the ability of the animals to main-
tain the concentrations of plasma proteins (Horowitz and Adler 1983; Horowitz

96
and Samueloff 1988). The latter may be influenced by such factors as a decreased
leakage of proteins across capillaries, an increased protein synthesis and the
shunting of blood to vascular beds that are less permeable. Cardiovascular adjust-
ments undoubtedly contribute to the maintenance of the circulation during
dehydration.

3 The Monotremes {Egg-Laying Mammals)

The monotremes are confined to Australia and New Guinea, where they occupy a
variety of contrasting habitats. The platypus is aquatic, living in lakes and rivers,
while echidnas live in areas ranging from deserts to tropical rainforests.
Most of our knowledge about the physiology of monotremes is based on ob-
servation of echidnas, especially Tachyglossus aculeatus. This mammal weighs
about 3 kg and in its native habitat is insectivorous, eating ants and termites.
The echidna, in common with the platypus, has a body temperature of only
30°C (Martin 1902) and a metabolic rate about half that expected in a placental
mammal of similar size (Schmidt-Nielsen et al. 1966b). The extraction of oxygen
from the inspired air is similar to that in other mammals (Bentley et al. 1967b)
so that its respiratory losses of water are expected to be less. Although the echidna
can maintain a constant body temperature at low environmental temperatures, its
thermal evaporative cooling at high temperatures is poor, since it neither sweats
nor pants under such conditions (Schmidt-Nielsen et al.1966b). The overall water
balance of echidnas with a natural diet of termites has been calculated (Bentley
and Schmidt-Nielsen 1967); it appears that, in their natural habitat, they proba-
bly require little or no water to drink. An investigation on echidnas maintained
under natural conditions . has shown this prediction to be remarkably close
(Griffiths 1978). However, when they were maintained in dry air drinking
occurred. The ability of the kidney to form a hyperosmotic urine is critical to the
maintenance of a positive water balance under such conditions. Dehydration
results in a decreased volume of urine, that may have a concentration of 2300
mosmoll- 1• This is achieved by tubular reabsorption of water and a decreased rate
of glomerular filtration. The manner of controlling changes in urine volume and
concentration is unknown, but the pituitary contains the placental antidiuretic
hormone, arginine-vasopressin, as well as oxytocin (Sawyer et al. 1960). The esti-
mated (in a 3-kg echidna) concentration of vasopressin in the pituitary is about
10-9 M kg- 1 body weight, which is less than that usually found in mammals (see
Follett 1963; Table 3.2).
The adrenal glands in monotremes do not show the distinct delineation into a
cortex of interrenal tissue and a medulla of chromaffin cells. Indeed, the echidna
adrenal is somewhat akin in its morphological arrangement to that in reptiles,
while the platypus has the form seen in marsupials and placentals (Wright et al.
1957). The adrenal is relatively small in the echidna in relation to its body weight
(Sernia 1980). Corticosteroid hormones are present in the peripheral circulation,
but at a very low concentration compared to other mammals. Corticosterone is
the major such steroid, while cortisol and aldosterone are present, but at even

97
lower concentrations (Weiss and McDonald 1965; Sernia 1980). The predomi-
nance of corticosterone is not a characteristic of the monotremes as cortisol is
the major such steroid in the platypus (McDonald et al.1988).A physiological role
for corticosteroids in regulating salt metabolism in the echidna is doubtful. When
they are not stressed they can survive for at least 20 weeks following adrenalec-
tomy (McDonald and Augee 1968). No detectable electrolyte or metabolic distur-
bances were observed in such animals. However, when exposed to cold
environmental conditions, they cannot adapt and they then die (Augee and
McDonald 1969). Nevertheless, they can be protected under such conditions by
the administration of glucocorticoids, which facilitate the mobilization of fatty
acids from fat stores. The synthesis of corticosteroids can be increased by the
administration of ACTH in the echidna. Angiotensin II increases the synthesis of
aldosterone. However, renin has not been detected in the plasma of these animals
(Reid 1971). Nevertheless, a juxtaglomerular apparatus and renin are present in
the kidney. The adrenal cortex in the echidna appears to be principally involved
in metabolic responses and the adaptation to stressful conditions. The absence of
mineralocorticoid effects may be a unique situation in mammals.

4 The Marsupials (Pouched Mammals)

Two families of marsupials live in the Western Hemisphere: the Didelphidae (o-
possums) and the Caenolestidae (shrew-like animals living in South America).
Most marsupials, however, live in the Australian region, where the contemporary
families occupy the variety of ecological niches on the continent, in a fashion that
parallels the manner in which placentals occupy similar places elsewhere. Various
species have adopted insectivorous, herbivorous and carnivorous diets. They may
be arboreal, like the possums, fossorial, like marsupial moles, or they may live in
a more conventional way on the surface. Large areas of Australia are desert with
little and irregular rainfall, combined with a high environmental temperature and
a low humidity. Other regions on the continent are covered with tropical rainfor-
est, while there are also many temperate areas with more equitable climates. The
marsupial fauna has occupied all these regions with success, often to the chagrin
of the sheep farmers, whose flocks may fare poorly compared to the indigenous
species. In many of the more barren regions, sheep and cattle, in contrast to mar-
supials, require supplements of trace elements, protein and water in order to
survive and breed.
Physiological knowledge about most of the 75 genera of Australian marsupi-
als is lacking, but a modest amount of information is available for some species,
especially members of the family Macropodidae. The macropods consist of 17
genera of kangaroos and wallabies, nearly all of which are herbivorous (the diet
of musky rat kangaroos includes worms and insects) and have a grazing manner
of life. They range in size from 500 g in the musky rat kangaroo to 70 kg in the
larger members of the genus Macropus.
Martin in 1902 reported that the metabolic rate of several marsupials was only
about one-third as great as would be expected in placentals of comparable size.

98
 That marsupials do indeed generally have a lower basal rate of oxygen consump-
tion than placentals has been shown in a variety of species (Dawson and Hulbert
1969; Arnold and Shield 1970). The basal rate of oxygen consumption is about
one-third less than predicted in a placental of the same size. This is accompanied
by a lower body temperature. It thus seems likely that evaporative water losses
from marsupials may be less than in placentals. The daily water consumption of
kangaroos is only about two-thirds that of placental mammals of a similar size,
which is consistent with such a water saving (Denny and Dawson 1975).
Some marsupials have labile body temperatures that change in a characteris-
tic cycle over the course of each day. This is well shown in the chuditch or western
native cat, Dasyurus geoffroii. The chuditch is a carnivorous marsupial weighing
1 to 2 kg, which has a wide geographic range throughout Australia, where it inhab-
its even the hot desert regions. It is nocturnal in its behaviour, coming out to hunt
for food in the evenings. The body temperature of these marsupials changes in a
parallel manner, declining to a minimum in late afternoon and rising as much as
4 oc in the evening (Arnold and Shield 1970). During the period of inactivity the
rate of oxygen consumption was found to be only two-thirds as great as predicted
in a placental of the same size. Red kangaroos commence their feeding activity
in the early morning, when their body temperature may be 3 oc below normal.
This adjustment appears to delay the need for evaporative cooling (Brown and
Dawson 1977). Such changes in the metabolic rate must result in a conservation
of calories and also a reduction in the rate of evaporative water loss. These phys-
iological adjustments could well assist the animal's survival, especially in its
desert habitats (Arnold and Shield 1970). ·
The kidneys of marsupials, like those of placental mammals, possess a loop of
Henle and can form hyperosmotic urine. The functioning of their kidneys appears
to be regulated also by hormones from the adrenal cortex and the neurohypoph-
ysis. The morphology of these endocrine glands, including the zonation of the
adrenal cortex, is similar to that of placental mammals. As in the latter mammals,
the principal secreted adrenocorticosteroids are cortisol and aldosterone, which
are usually accompanied by smaller amounts of corticosterone (Oddie et al. 1976;
McDonald and Martin 1989). However, the compound F I compound B ratio
(cortisol I corticosterone) varies from 40 in the pademelon wallaby to 0.7 in the
common wombat. It also varies considerably in placental mammals; it is 20 in a
monkey and 0.1 in rabbits and the laboratory rat (Bush 1953). Such variations can
reflect genetic differences in the enzymes involved in their synthesis. However,
the ratio of their secretion is also influenced by the prevailing level of adreno-
cortical activity and the presence of ACTH. Some marsupials also secrete signif-
icant quantities of 11-deoxycortisol, which in placental mammals is a precursor
of cortisol. A secretion of 11-deoxycorticosterone, which is a precursor of aldos-
terone, may also occur. Marsupials possess ACTH and the renin-angiotensin
system and they contribute, as in placental mammals, to the regulation of the
activity of the adrenal cortex (Reid and McDonald 1969; Simpson and Blair-West
1971; Blair-West and Gibson 1980).
The neurohypophysial hormones in marsupials are, rather surprisingly, more
diverse in their structures than those in placental mammals or the echidna (Table
3.1). Anomalies in the ratio of vasopressin I oxytocin had earlier suggested the

99
Table 3.1. Phyletic distribution of the neurohypophysial hormones in marsupials

Family and species AVP LVP pp OT MT

Didelphidae
Opossums (American)
Didelphys virginiana + + + +
D. marsupialis + + +
Macropodidae
Kangaroos and wallabies
Macropus rufus + + +
M. eugenii + + +
Setonyx brachyurus + + +
Phalangeridae
Brushtail possum
Trichosurus vulpecula + +
Peramilidae
Bandicoot
Isoodon macrourus + + + +
Dasyuridae
Native cat
Dasyurus spp. + +
Phascolarctidae
Koala
Phascolarctos cinereus + +

AVP = 8-arginine vasopressin; LVP = 8-lysine-vasopressin; PP = 2-phenylalanine-8-arginine-

vasopressin (phenypressin); OT = oxytocin; MT = 8-isoleucine-oxytocin (mesotocin). (After
Chauvet et al. 1983; Rouille et al. 1988; Bathgate et al. 1992; Acher 1996).

possibility that such hormones may be different in marsupials (Bentley 1971a).

Most placentals and echidnas typically secrete 8-arginine-vasopressin (AVP,
ADH) and oxytocin. Pigs and the Peru strain of mice secrete 8-lysine-vasopressin
(LVP) instead of AVP. The marsupial neurohypophysis has been shown to contain
up to four different such peptide hormones in a single individual. In the north-
ern bandicoot (family Peramilidae) the neurohypophysis contains AVP and
oxytocin, but there is in addition also LVP and a homologue of oxytocin,
8-isoleucine-oxytocin (mesotocin) (Rouille et al.1988). The latter observation was
of considerable interest, as this peptide, which has a biological activity similar to
oxytocin, was formerly only known to occur in non-mammalian tetrapods and
lungfish. The duplication of the antidiuretic hormones and oxytocin appears to
have arisen as a result of gene duplication. A similar situation has been observed
in the North American Virginia opossum (Table 3.1). Lysine-vasopressin, but not
AVP, is present in kangaroos (family Macropodidae). In this family of marsupials
it is accompanied by a novel second antidiuretic hormone, 2-phenylalanine-AVP
(phenypressin). When tested for their antidiuretic effects in various species, AVP,
LVP and phenypressin all display significant activity, which has probably con-
tributed to their evolutionary survival. Thus, marsupials appear to have a plethora
of antidiuretic hormones. Receptors for vasopressin and oxytocin have been iden-
tified in the brushtail possum (Bathgate and Sernia 1995). Their pharmacologi-

100
 10
10

10

Fig. 3.3. Map of Australia showing the locations and average annual rainfall (in inches; 1 inch
= 2.54 em) in the areas where the quokkas (Setonix brachyurus), euros (Macropus robustus) and
red kangaroos (Megaleia (Macropus) rufus) have been studied under natural field conditions.
E Ealey (euros); N Newsome (reds); D Dawson (reds and euros) areas. R Rottnest Island
(quokkas)

cal binding to various neurohypophysial peptides differs from those of the recep-
tors in a placental mammal (the laboratory rat).
Information relevant to marsupial osmoregulation is available from four pop-
ulation groups, one living in a temperate and three in desert areas.
Professor Harry Waring initiated such studies on a small (2- to 5-kg) wallaby,
the quokka, Setonix brachyurus, that lives in a temperate, but seasonally dry,
habitat on Rottnest island, 18km from the coast of southwest Australia (see Fig.
3.3). Today, Setonix is principally confined to this island, though a few isolated
pockets of the population remain on the mainland. The annual rainfall on Rot-
tnest is 75 em, of which 68 em falls between March and October, so that in the
warm summer months, when the temperature may rise to 38 °C, little rain falls.
The vegetation dries out during this period. There are two distinct populations
of quokkas on the island (Jones et al. 1990). One occupies the extreme west end
where there are no perennial supplies of drinking water. The other, larger, popu-
lation lives in the region of several salt lakes on the eastern side of the island,
where fresh and brackish water soaks are present. By 1990, only one freshwater
pool still existed, the remainder being brackish. The quokkas living under sea-
sonally arid conditions on Rottnest Island appear to be the descendants of main-

101
land animals that originally lived near swamps. However, the Rottnest population
has adapted to life in more arid circumstances. Their physiology has been studied
over a period of more than 50 years both in the laboratory and in their native
island refuge.
Martin in 1902 reported that marsupials do not regulate their body tempera-
ture adequately in hot environments, an observation that is relevant to their water
loss in such situations. However, it was found that Setonix brachyurus regulated
its body temperature as efficiently as placental mammals at temperatures up to
40°C (Bentley 1955; Bartholomew 1956}. This regulation is accompanied by sweat-
ing, salivation and panting, and results in a substantial loss of water. When Setonix
is dehydrated, such evaporation of water is reduced by 40% (Bentley 1960) an
adaptation reminiscent of that in placentals like the rat, camel and oryx. It seems
likely that this decrease in water loss is mediated by a reduction in the metabolic
rate, but neither this, nor its possible relationship to the secretions of the thyroid
gland has been investigated. Setonix is not exceptional among marsupials in its
ability to regulate its body temperature; members of this group are as efficient in
this respect as placental mammals.
During the dry summer period, the concentrations of urine of the quokkas
increase to levels two to three times as great as those observed in the wet winter
period. Dehydrated quokkas can form a hyperosmotic urine with a concentration
of 2000 mosmoll- 1 (Bentley 1955), which is comparable to the ability of placen-
tal mammals. Exposure of Setonix to heat, with accompanying dehydration, was
found to result in the appearance of an antidiuretic substance, presumably lysine-
vasopressin, in the plasma (Robinson and MacFarlane 1957}. The injection of
vasopressin into hydrated quokkas reduces the urine flow (Patricia Woolley,
quoted by Waring et al. 1966}, and increases its concentration (Bentley and Shield
1962). Severing the supraopticohypophysial tract in the tammar wallaby results
in the secretion of copious, dilute, urine (Bakker and Waring 1976}. There is thus
strong presumptive evidence to suggest that urine flow in this marsupial is regu-
lated, as in placentals, by the release of antidiuretic hormone that acts on the
kidney.
The water metabolism, kidney function and concentrations of lysine-
vasopressin in the plasma of Rottnest Island quokkas has been measured in late
summer prior to seasonal rains (Jones et al. 1990; Bradshaw 1999). The two pop-
ulation groups on the island were studied; one from the west end, where there is
no drinking water, and the other from the area around the salt lakes, where brack-
ish water was available. The turnover of water was nearly 2.5 times greater in the
animals from the salt lakes area. Their production of urine was also greater. The
quokkas from the salt lakes area secreted urine with a concentration of about 1000
mosmoll- 1 • In the west end animals this concentration was 1250 mosmoll- 1 • The
plasma of the latter was also more concentrated. Plasma concentrations of lysine-
vasopressin were measured. The mean concentration was 89pgml- 1 in the west-
end quokkas and 36pgml-1 in those from the salt lakes area. In the late summer
period the west-end quokkas were in poor condition but, nevertheless, they can
survive without drinking water. It was suggested that the availability of brackish
water, combined with its efficient use, is important for the maintenance of the
better condition of the salt-lakes quokkas.

102
 It has been suggested that the quokkas on Rottnest Island may drink sea-water
during the summer drought period and so possibly acquire a considerable excess
of salt. These animals can concentrate urinary electrolytes to about 800mEq.l- 1,
which is higher than the level of 560 mEq.l-1 in sea-water. Some quokkas, in
extreme circumstances when no other fluid is available, drink small amounts
of sea-water and make a net gain of osmotically free water (Bentley 1955).
However, it seems unlikely that this species normally drinks sea-water, though
a similar small wallaby, the tammar, Macropus eugenii, apparently can do so
(Kinnear et al. 1968).
The concentrations of lysine-vasopressin in the plasma of two species of
desert-dwelling wallabies have been measured during the dry and wet seasons
(Bradshaw et al. 2001). The spectacled hare-wallaby, Lagochestes conspicillatus, is
now confined to Barrow island off the NW coast of Australia while Rothschild's
rock-wallaby, Petrogale rothschildi, is endemic to the adjacent Pilbara region of
the mainland. Summers are very hot in this region and seasonal drought condi-
tions often prevail. During the daytime the rock-wallabies shelter in cool caves
among rocky outcrops while the hare-wallabies seek refuge in clumps of Spinifex
grass. The environmental temperatures often reach 40 oc in the latter. Both species
can form a highly concentrated urine: up to 3600mosmolkg-1 water. In the dry
season plasma lysine-vasopressin levels increase considerably in the hare-
wallabies but they remain low in the rock-wallabies. The urine volumes in both
species decline at this time. The change in urine volume and increases in its
concentration are related to the plasma vasopressin levels in the hare-wallabies
but not in the rock-wallabies. Instead, the latter experience a decrease in renal
plasma flow and the GFR. This change in renal haemodynamics and the selection
of a cooler microhabitat may then obviate a role for vasopressin in regulating the
composition of the urine.
The first studies to be carried out on the endocrine regulation of sodium and
potassium metabolism in Australian marsupials were those of Buttle et al. (1952).
Earlier work on the American opossum, Didelphis virginiana, suggested that the
adrenal cortex may not be as important to marsupials as to placental mammals,
since this species could, in certain circumstances, survive adrenalectomy for pro-
longed periods, with little or no change in electrolyte level. Jenny Buttle and her
collaborators found that adrenalectomy in the quokka was usually fatal within 2
days. Death was accompanied by elevated plasma potassium and decreased
plasma-sodium concentrations. The mean survival time could be increased two
or three times by either giving the quokkas 1o/o sodium chloride solutions to
drink, or by injecting them with a corticosteroid, deoxycorticosterone acetate. The
subsequent administration of newly available preparations of cortisol and aldos-
terone to adrenalectomized quokkas showed that they could be maintained inde-
finitely by these corticosteroids (McDonald and Bradshaw 1993). When given
together, they maintained plasma Na+ concentration, renal plasma flow and the
GFR, which otherwise fall in their absence. Cortisol also maintained plasma
glucose and increased food intake. Similar observations have been made on
several other marsupials (McDonald and Martin 1989). They include the brush-
tail possum (Reid and McDonald 1968) and the red kangaroo (McDonald 1974).
The latter develops a sodium appetite following adrenalectomy and if a saline

103
solution is provided for them to drink, they survive indefinitely without hormone
supplements.
When quokkas are maintained on a sodium-replete diet, the concentration of
aldosterone in the plasma is low, about 2ng {100mlt1, but after 7 days on a
sodium-deficient diet the concentrations increase to about 17 ng {100 mlt 1 (Miller
and Bradshaw 1979). Urinary Na+ excretion is very low in the latter quokkas, but
the concentrations in the plasma were maintained at normal levels. The concen-
trations of aldosterone in the plasma were also measured over a 2-year period in
quokkas living in their native habitat on Rottnest Island. The values did not vary
in the different seasons and were generally maintained at a level of 7 to 8 ng
{100 mlt 1, which is somewhat higher than in sodium-replete animals. Urinary Na+
excretion in the quokkas living on Rottnest Island averaged 8 mEq. kg- 1 day- 1 com-
pared to 23 mEq. kg- 1 day- 1 in sodium-replete laboratory animals. Under natural
conditions the quokkas appear to be utilizing aldosterone to limit urinary losses
of sodium.
The water metabolism of two large species of kangaroo has been studied in far
hotter and drier areas than those occupied by Setonix. Tim Ealey led a series of
ecological and physiological investigations on a wild population of the hill kan-
garoo, or euro, Macropus robustus, living in a hot dry desert region of northwest
Australia (Fig. 3.3). Alan Newsome carried out a similar investigation on the red
kangaroo, Megaleia (or Macropus) rufus, living in an arid central region of the
continent near Alice Springs. The average annual rainfall in both the areas is about
25 em, most of it falling during the summer months. The rain, however, is spo-
radic and unreliable, and both areas may undergo periods of drought when little
rain falls for periods of 3 or 4 years. The summer temperature is high, the average
daily maximum often being greater than 40 °C for many weeks, and may rise to
49°C. The relative humidity usually is low, so that the potential evaporation is
high. Despite these osmotically adverse conditions the kangaroos in these areas
continue to survive and multiply. A man lost in these regions in the height of
summer can expect to survive for less than 1 day (Adolph 1947), so the adapt-
ability of the kangaroos is impressive. Both the euro and the red kangaroo may
form a highly concentrated urine, which can be 2700 mosmoll- 1 in the red kan-
garoo (A. Newsome, quoted by Schmidt-Nielsen 1964a) and 2200 in the euro
(Ealey et al. 1965). Such an ability must aid water conservation by these animals
but is not a predominant factor in their survival. Ealey and his collaborators
observed that euros can withstand dehydration equivalent to 30% of their body
weight, and that they reduce evaporation by sheltering in rocky caves during the
heat of the day. Euros drink periodically, and even during hot dry periods only
come in to obtain water on an average of once every 3 days. During the inter-
vening period they incur a water deficit equivalent to about 12% of their body
weight. Newsome (1965a,b; 1971) found that the red kangaroos also drank only
sporadically, apparently gaining most of their water from their diet, which con-
sists preferentially of succulent green shoots of the herbage. The animals limit
evaporation during the day by seeking the shelter of bushy woodlands and avoid-
ing the open plains. During the dry season kangaroos often utilize drinking water
at man-made sites provided for livestock. The degradation of the surrounding
natural rangelands has been partly attributed to the presence of kangaroos. They

104
can, with such water available, continue to breed during hot dry seasons, when
under more natural conditions such activity would cease. Limiting their access to
artificial drinking points has been utilized as a strategy to control their prolifer-
ation (Norbury and Norbury 1992}.
Terry Dawson (Dawson et al. 1975} and his collaborators carried out a similar
survey of the water metabolism and diet in natural populations of red kangaroos
and euros living in a seasonally arid region in eastern Australia (Fig.3.3}. They
compared these marsupials to domestic sheep and wild goats. The water turnover
of the placental mammals was three to four times greater than that of the kanga-
roos. The latter also needed to drink much less often. The principal reasons for
the differences appear to be metabolic, physiological and behavioural adaptations
of the native marsupial fauna to the local conditions.
The grasses of the central Australian regions are deficient in sodium compared
to those in coastal areas (Denton 1965), so that conservation of this solute could
be of particular importance to many kangaroos. However, there is no definitive
information about this for the red kangaroos living in the Newsome study area.
The urine (Newsome, quoted by Schmidt-Nielsen 1964a} of these animals has a
Na/K ratio of 0.13, while the euros in the Ealey study area exhibit a ratio of 0.33.
This suggests that relatively more sodium may be available to the euro than the
red kangaroo. Two populations of the grey kangaroo, Macropus g iganteus, living
on grasses with contrasting contents of sodium, have been studied by Coghlan
and Scoggins (1967}. One group of these kangaroos lives in the coastal areas of
southeast Australia, where the grasses contain most than 150 mEq sodium kg- 1 dry
weight, and the other occupies the Snowy Mountain plains, where the herbage
contains less than 10 mEq sodium kg- 1 dry weight. Aldosterone, cortisol and cor-
ticosterone have been identified in the blood of the red kangaroo (Weiss and
McDonald 1967} as well as of the grey kangaroo. The red kangaroos were studied
in the laboratory and, while aldosterone was secreted at rates comparable with
those seen in placentals, the cortisol levels were somewhat lower. Rates of corti-
costeroid secretion were measured in grey kangaroos caught in the field and it
was found that animals living in the sodium-deficient Snowy Mountains area have
blood aldosterone levels eight times as great as those from the sodium-replete
coastal regions. There was little difference in the blood levels of cortisol or corti-
costerone. The zona glomerulosa (which secretes aldosterone) in the adrenal cor-
tices of the animals from the Snowy Mountains plains was larger than that in the
other group.

S The Placental Mammals

Generically and numerically, the placentals are the predominant group of

mammals. All of the marine and most aquatic mammals belong to this group.
They are present in all of the world's deserts. The placentals have thus adapted to
a wide range of differing osmotic circumstances.
The Rodentia make up about one-third of all placental genera. This order has
a very cosmopolitan distribution, occupying diverse habitats including the deserts

105
of Africa, Asia, America and Australia, where, with the possible exception of the
latter area, they are the principal mammals present. Osmoregulatory problems in
such dry hot areas result in the exclusion of most mammals, except certain
rodents that are equipped with behavioural and physiological adaptability. Knut
and Bodil Schmidt-Nielsen investigated the water metabolism of the banner-
tailed kangaroo rat, Dipodomys spectabilis, and revealed the manner in which this
little rodent lives in a desert without drinking water. The kangaroo rat belongs to
the family Heteromyidae, which is confined to the New World; it lives in the
deserts of the western United States and parts of Mexico. Its ability to survive and
thrive on a diet of air-dried seeds and vegetation, without requiring water to
drink, is the result of several adaptations that have subsequently been shown to
exist in other rodents occupying comparable ecological situations elsewhere. The
principal adaptation allowing the kangaroo rat to live under such conditions is
its small evaporative water loss. Rodents do not sweat or pant, and thus have a
limited ability to undertake thermal cooling; they may allow their body temper-
ature to rise somewhat in hot conditions (Schmidt-Nielsen 1964b). Obligatory
losses of water that take place by evaporation from the respiratory tract are
reduced in the kangaroo rat and white rat by utilizing a countercurrent heat-
exchange mechanism in the nasal passages to cool the expired air (Jackson and
Schmidt-Nielsen 1964). Such cooling reduces its content of water vapour. Rodents
living in hot desert conditions have adopted patterns of behaviour that can reduce
their need for evaporative cooling. Aided by their relatively small size, they usually
seek refuge in underground burrows, crevices in rocks and nests in dense vege-
tation. The environmental temperature is usually lower and the relative humidity
higher under such conditions than they are in the outside habitat. Many such
rodents are nocturnal and so avoid the heat of the day. Species that are active in
the daytime may make only brief forays out of such refuges. After their body tem-
perature rises, they return to them to cool off. Such activity is described as shut-
tling or crepuscular behaviour. These rodents thus reduce the need for evaporative
cooling. Some rodents reduce their metabolic rate and body temperature, and aes-
tivate in their burrows in late summer. This period of dormancy may be prolonged
to become one of hibernation over the winter period. It occurs in some under-
ground squirrels (genus Citellus) such as those that live in the deserts of the south-
west United States. A daily torpor, when the temperature decreases by only a few
degrees, has been observed in a number of Australian marsupials (Geiser 1994).
It also occurs in bats that live in arid regions (Carpenter 1968). Under such con-
ditions the energy reserves of the animals are extended and evaporative water
loss is reduced (Schmidt-Nielsen 1964a).
Rodents, especially those living in arid areas, conserve additional water by
forming a highly concentrated urine and relatively dry faeces. Not all desert
rodents can, however, achieve a positive water balance while eating a dry diet, and
some must obtain food containing a substantial amount of free water. The pack
rat, Neotoma, like the kangaroo rat, lives in the deserts of the western United States
but eats cactus plants, while the North African sand rat, Psammomys obesus, sub-
sists on succulent halophytic vegetation (Schmidt-Nielsen 1965a,b ).
Neurohypophysial peptides, arginine-vasopressin and oxytocin, have been
identified in the four species of rodents that have been examined, including the

106
 white rat, Rattus norvegicus, the kangaroo rat, Dipodomys merriami, and the
guinea pig, Cavia porcellus (see Sawyer 1968). Arginine-vasopressin has also been
identified in five strains of mice (Mus musculus), while in the Peru strain, lysine-
vasopressin has been found (Stewart 1968).
The neural lobe of rats can be destroyed by cutting the supraoptico-hypophysial
tract and allowing the peripheral tissue to degenerate. Such animals form large
volumes of dilute urine which they are unable to concentrate (diabetes insipidus).
Valtin and his colleagues (1962) have identified a strain (Brattleboro) of rats with
hereditary diabetes insipidus due to the specific absence of vasopressin, although
oxytocin is still present (Sawyer et al. 1964). The injection of vasopressin into such
laboratory rats with diabetes insipidus results in a reduction of their urine volume
and increases in its concentration. Laboratory rats are a mutant strain of the brown
rat, Rattus norvegicus, which in its indigenous habitat in East Asia lived in wetlands
along the banks of streams and rivers. Vasopressin has been identified in the
plasma of a variety of other rodents. Apart from laboratory rats and mice, they
include several species that live in the deserts of the United States and the Middle
East, such as kangaroo rats (Ames and van Dyke 1952), jerboas, gerbils (El-
Husseini and Haggag 1974; Baddouri et al.1984) and spiny mice (Castel et al.1974).
The concentrations of vasopressin in the plasma of the desert species are usually
maintained, under natural conditions, at far higher levels than those that occur in
dehydrated laboratory rats (Dicker and Nunn 1957). Such concentrations of this
hormone can, however, be reduced by hydrating the animals (Cole et al. 1963).
Dehydration of laboratory rats results in a ten fold rise in the concentration of
vasopressin in the plasma, an increase in its excretion in the urine and a depletion
of its stores in the neurohypophysis (Dicker and Nunn 1957). Kangaroo rats,
despite normally maintaining plasma levels of vasopressin that are far greater
than in laboratory rats, maintain stores in their neurohypophyses that are five
times greater (Table 3.2). Vasopressin is also released more readily in response to
increases in plasma concentration in the kangaroo rats than in the laboratory
rats (Stallone and Braun 1988).Mammals that normally live under xeric conditions
appear generally to maintain larger stores of vasopressin in their neurohypophy-
ses. There are also associated differences in their neural lobes, which may be
larger (Fig. 3.4). Chronic water deprivation has also been observed to produce a
hypertrophy of the neural lobe in rodents (Castel and Abraham 1969). The long-
term regulation of vasopressin synthesis appears to have become adjusted to the
everyday needs of xeric species.
The ability to limit urinary water loss may vary among species in relation to
the dryness of the normal habitat (Table 1.6). Extrarenal water loss, however, pre-
dominates, and in white rats kept in the laboratory without water it is five times
greater than the urinary loss, while in the kangaroo rat it is 2.5 times as great (see
Dicker and Nunn 1957). Under such conditions, these rodents form hyperosmotic
urine, which in the white rat may be nine times more concentrated than the
plasma, and in the kangaroo rat 14 times that level (Schmidt-Nielsen 1964a). In
the absence of neurohypophysial antidiuretic hormones, urine that is isosmotic
to plasma is formed, so that the total water loss under such conditions would be
expected to increase considerably. Urinary loss would then be more than twice as
great as the extrarenal loss.

107
Table 3.2. Quantities of vasopressin in the neurohypophysis of rodents

wt (g) nmolkg-' body wt

Mus musculus• 20 7
(mouse)
Rattus norvegicus• 250 3.7
(rat)
Aplodontia rufab 1000 0.8
(Mountain beaver)
Cavia porcellus' 400 3.2
(Guinea pig)
Dipodomys merriamid 40 18
(kangaroo rat)

a Follett (1963}.
b Dicker and Eggleton (1964}.
' Dicker and Tyler (1953}.
d Ames and Van Dyke (1950}.

Removal of the adrenal gland from laboratory rats results in death, usually
within a few days. This results largely from a depletion of the sodium and an
excessive accumulation of potassium, due to an inadequate integration of renal
and colonic electrolyte excretion in the absence of the adrenal corticosteroids.
Adrenalectomy has also been carried out in the kangaroo rat, Dipodomys
spectabilis, with the same results, that are characteristic of the mammals (Cole et
al. 1963). The desert gerbil, Gerbillus gerbillus, dies within 7 days of adrenalec-
tomy, but this period can be extended by injecting the animals with cortisone and

Neural lobe as percentage of whole pituitary

10 20 30 40 50

Red sq uirrei
Pocket mouse
Merriam's kangaroo rat
Birch mouse
Mojave kangaroo rat ~
Desert rat (Meriones) 1 - - ----.--'
Water vole
• Laboratory rat
Bank vole
Long· tailed field mouse d' Neural lobe
0 Glandular lobe
+Laboratory ral

Fig. 3.4. Comparison of the relative size of the neural lobe in several species of rodents. H Hiber-
nating; D desert-living species; • non-hibernating rodents of temperate zone habitat. (Howe
and Jewell1959. Redrawn from Enemar and Hanstrom 1956}

108
feeding them a diet with a high content of sodium chloride (Burns 1956). The
adrenal cortex of laboratory rats secretes aldosterone and corticosterone, but
little, if any, cortisol. Bush {1953) found that the ratio in the secretion of cortisol
I corticosterone (compounds FIB) was less than 0.05. The banner-tailed kanga-
roo rat, on the other hand, also forms cortisol and has an F I B ratio of about 1.4.
Bush, after comparing F I B ratios in a number of species of placentals which
normally have a differing diet and way of life, concluded that such differences
are probably genetically determined variations of the biosynthetic pathways
in the adrenal cortex, and cannot be related to differences in the role of the
corticosteroids.
Plasma 17-hydroxyxcorticosteroid concentrations (principally consisting of
cortisol and corticosterone) have been measured in two rodents, a jerboa,Jaculus
jaculus, and a gerbil, Gerbillus gerbillus, that live in arid areas in the Middle East
(Haggag and El-Husseini 1974}. The concentration of these corticosteroids was
greater in the hot summer months than in the winter, and increased when the
animals were maintained on dry diets. Their release in response to ACTH or dehy-
dration was greater in the jerboa, which is a more desert-adapted species than the
gerbil. Such secretion of corticosteroids may be related to stress resulting from
the hot conditions and dehydration. The renin-angiotensin system in mammals
can be activated by dehydration (Blair-West et al. 1983). This response appears to
occur following a decrease in blood volume and results in a rise in the concen-
tration of angiotensin II in the plasma. This hormone may initiate compensatory
responses including a secretion of aldosterone, peripheral vasoconstriction, a
stimulation of thirst, drinking and sodium appetite. Such effects are well known
in laboratory rats. However, species of rodents that live under xeric conditions,
including kangaroo rats, Mongolian gerbils and Australian hopping mice, appar-
ently do not appear to utilize the RAS to help maintain their body fluids dur-
ing dehydration (Wright and Harding 1980; Weaver et al. 1994}. The drinking
response to injected angiotensin II in such desert rodents is also often poor
(Kobayashi et al. 1979}. Species that were found to be insensitive to administered
angiotensin II include the house mouse, Syrian hamsters, chipmunks and Mon-
golian gerbils. Wild rabbits, captured in Australia, also failed to exhibit a drink-
ing response to injected angiotensin II (Denton et al. 1985). (However, sodium
appetite was stimulated.) Marsupial mice, Antechinus stuartii, normally do not
drink in nature, and also fail to exhibit a drinking response to angiotensin II
(Blair-West et al. 1983). Nevertheless, despite being unable to detect a role for the
RAS in response to dehydration, the normal, basal, levels of angiotensin II in the
plasma were found to be much higher in kangaroo rats and Mongolian gerbils
than in laboratory rats (Wright and Harding 1980}. Dehydration results in a five
fold increase in the concentration of angiotensin II in the plasma of laboratory
rats, but it is still then only 50pgml- 1 compared to 110pgmt 1 in water-deprived
kangaroo rats. The possible role of such high concentrations of angiotensin II in
the plasma of kangaroo rats invites further investigation.
The sea provides an ecological niche for many mammals, including the Cetacea
(whales and dolphins}, Sirenia (manatees and dugong) and several families of the
Carnivora (seal, sea lions and sea otters). There is even a fishing-bat (Pizonyx
vivesi) which, although not a regular swimmer, manages to subsist, without fresh

109
water, on the fringes of a marine habitat (Carpenter 1968). Seals and sea lions
spend prolonged sojourns on land during their breeding seasons, though such
visits by sea otters are quite brief. The other orders of marine mammals are
entirely aquatic, though some, such as the West Indian manatee (Trichechus
manatus), live mainly in fresh water. (Ortiz et al. 1999). Indeed, some species live
entirely in fresh water, such as dolphins that live in the Amazon, Ganges and
Yangtze rivers.
The mammals that live in the sea clearly do so without access to fresh drink-
ing water. Many species eat fish, which have a relatively low salt content. However,
many whales and the sea otters eat invertebrates that are isosmotic to sea-water,
while the sirenids are herbivores. Whales and seals live for prolonged periods,
during migrations and breeding, by utilizing large reserves of body fat. The milk
of marine mammals has a high fat content. Such dietary observations and
measurements of the salt and urea content of their urine indicate that feeding
animals can gain substantial amounts of preformed water, as well as metabolic
water, from the consumption of fish. Invertebrates and sea grasses provide a
more frugal source of such water due to their relatively high salt content. Fasting
marine mammals and their suckling young appear to gain substantial amounts
of metabolic water from the metabolism of body fat. (Fat has been called a
water storage depot in such animals.) Seals and manatees are known to drink
fresh water when it is available. However, whether marine mammals regularly
drink sea-water is uncertain. Measurements of the salt contents of their urine and
their water turnover rates suggest that such behaviour (mariposia) is rare.
However, the drinking of sea-water has been observed in seals (Gentry 1981;
Skalstad and Norday 2000), sea otters (Costa 1982), fish-eating bats (Carpenter
1968) and dolphins (Hui 1981). Seals and dolphins may drink some sea-water
"accidentally", such as during feeding and in response to stress, but it is
generally considered unlikely that they normally indulge in this behaviour in
order to maintain a positive water balance. It has been suggested that the
consumption of small amounts of sea-water may "expand the urinary osmotic
space" and so facilitate the excretion of urea (Carpenter 1968; Hui 1981; Costa
1982). It may also help them to maintain mineral balance (Skalstad and Norday
2000). Urinary salt concentrations in marine mammals usually do not exceed that
of sea-water (Smith 1936; Bentley 1963), but such concentrations have sometimes
been observed (Carpenter 1968; Costa 1982). Gains of osmotically free water
could occur on such occasions. Marine mammals appear to have a relatively
impermeable skin. Small percutaneous movements of water, though not sodium,
have been observed in dolphins (Hui 1981). Respiratory water losses are expected
to be low in an aquatic environment. It is generally considered that marine
mammals can usually maintain their water balance without drinking (Krogh
1939; Smith 1951).
The kidney appears to be the principal organ for regulating water and salt
excretion in marine mammals. No extrarenal salt excretory mechanisms, such as
exist in fish, marine reptiles and sea birds, have been identified. Hyperosmotic
urine appears to be habitual in marine mammals except in manatees when they
enter fresh water (Ortiz et al. 1998). It has been observed that the kidneys of
marine mammals are very large as compared to those of terrestrial species

110
 (Beuchat 1996). The physiological significance of this observation is not known
but possibly reflects their habitual excretion of large amounts of salt. Seals (Smith
1951) and dolphins (Malvin and Rayner 1968) have been observed to have an
especially labile GFR and renal plasma flow. This capacity may be principally
related to the ability to shunt blood from the viscera to the brain during diving.
However, large increases in GFR and renal plasma flow have been observed
in seals and dolphins following feeding. Such changes could be facilitating salt
excretion.
Sporadic observations have been made on the possible roles of vasopressin,
renin and adrenocorticosteroids in regulating renal water and salt excretion in
marine mammals. Arginine-vasopressin and oxytocin have been identified in the
neurohypophyses of fin-back whales (Chauvet et al. 1963). Vasopressin has also
been measured in the pituitaries of dolphins (Tursiops truncatus) (Malvin et al.
1971 ). Cortisol, corticosterone and aldosterone have been identified in the adrenal
cortex of whales (Race and Wu 1961; Carballeira et al. 1987) and the California
sea lion (DeRoos and Bern 1961).
Vasopressin has been measured in the plasma of grey seals (Skog and Folkow
1994), elephant seal pups (Ortiz et al. 1996), West Indian manatees (Ortiz et al.
1998) and bottlenose dolphins (Ortiz and Worthy 2000). Early attempts, using
bioassays, to measure it in the plasma of dolphins and a killer whale found only
concentrations that were barely detectable (Malvin et al. 1971). Injected vaso-
pressin has been observed to decrease the urine volume of harbour seals (Bradley
et al. 1954). The infusion of mannitol into grey seals was found to increase the
plasma concentrations of vasopressin (Skog and Folkow 1994). The plasma con-
centration of vasopressin has also been shown to increase in the grey seals when
they are deprived of food and water for 5 days. The levels of this hormone in
plasma rise in manatees after they enter sea-water (Ortiz et al. 1998). Thus, vaso-
pressin could be contributing to the regulation of urine flow in at least some
marine mammals. Its site of action in the kidney is unknown. However, the
administration of this hormone had no effect on the GFR in seals, suggesting that
a renal tubular response is occurring (Bradley et al. 1954).
Plasma renin activity increases during fasting in dolphins and decreases after
feeding them a sodium-enriched diet (Malvin et al. 1978). In West Indian mana-
tees the concentration of renin in the plasma is lower when they are in sea-water
than fresh water (Ortiz et al. 1998). The sodium concentration in their urine
declined when they were in fresh water. Plasma renin activity has also been
observed to increase in Northern elephant seal pups during their prolonged post-
weaned fast (Ortiz et al. 2000). The higher renin activity was correlated with
increases in the levels of aldosterone in the plasma in all these species. The plasma
concentration of aldosterone in harp seals and hooded seals decreases when they
are kept in sea-water and rises in fresh water (Skalstad and Norday 2000). These
observations suggest that the renin-angiotensin system and the release of aldos-
terone are responsive to the sodium levels in marine mammals.
Marine mammals appear to have retained the hormonal mechanisms for
regulating renal water and salt excretion that were developed in their terrestrial
forebears.

111
Chapter 4

The Birds

Birds are the most cosmopolitan of the vertebrates. The ability to fly confers on
them a mobility that is matched in other vertebrates only by the bats. Some avian
species have, however, lost the ability to fly, or do so to little effect. Flightless birds
include the ostriches, kiwis, cassowaries, emus and rheas, while many other
species like the domestic fowl are aviatorially inept. Some birds, like the penguins
and auks, use their wings for propulsion under water. Birds thus may live a
predominantly terrestrial or marine existence or they may also utilize the skies
above such areas. Geographically, birds are found on the most remote oceanic
islands, in dry continental desert regions, and in tropical and temperate areas
where water is abundant. They can indeed live, and thrive, in a variety of osmotic
environments.
The osmotic problems of birds are basically like those of mammals; their
osmotic anatomy is similar, they occupy the same geographical regions and
habitats and they are also homoiothermic. Their needs for water and salts are thus
potentially comparable, but differences in their physiological and morphological
characteristics may modify their respective requirements. Most birds are smaller
than mammals, so that they more often experience the difficulties inherent in a
large surface area to body weight ratio. The body temperature in birds is often in
the region of 40 to 42 oc, which is 3 or 4 oc higher than that of most mammals.
This reflects a metabolic rate that is higher than that of mammals, and so
modifies heat exchanges with the environment. Flight results in metabolic
burdens which are completely unfamiliar to mammals (except possibly the bats),
and this is reflected in increased respiratory gas exchange, with an accompany-
ing additional water loss. The mobility conferred by flying may, however, be a
considerable osmotic advantage, as it allows birds to travel rapidly for long dis-
tances to suitable feeding and watering places. This may be a relatively local
commuting, or it may take place between major geographical regions, in which
seasonal changes in environmental temperature and available food and water
may occur.
The birds exhibit a number of other physiological features relevant to their
osmoregulation, that they share with either the mammals or their phyletic pro-
genitors, the reptiles. Both the birds and mammals, in contrast to the reptiles, can
form a hyperosmotic urine. However, in birds, the maximal concentrations are
not as great as usually seen in mammals, but they conserve additional renal water
by converting most of their catabolic nitrogen to uric acid. Most reptiles are sim-
ilarly uricotelic. While in the mammals the kidney is the principal route for excre-
tion of salts, some birds and reptiles can also secrete such solutes as hyperosmotic
solutions from cephalic "salt" glands. Birds, like reptiles, but in contrast to

113
mammals (except the monotremes), are oviparous, and it can be conjectured that
this could influence the pattern of their osmoregulation. The rapid production of
a clutch of eggs containing all of the water and salt necessary for an extended
period of embryonic growth would seem to result in a more acute need for water
and salt than embryonic development in utero. Tending and incubating such eggs
temporarily restricts the movements of birds so that breeding can only occur in
a place and time of adequate proximal supplies of food and water.
Erik Skadhauge provided a landmark monograph on the osmoregulation of
birds (Skadhauge 1981). An excellent collection of works in progress was pre-
sented in 1989 by Hughes and Chadwick.
Birds have the same complement of osmoregulatory hormones as mammals, but
their chemical structures in the two phyletic groups often differ. Their physiologi-
cal roles in regulating water and salts, which mainly involve the kidneys and gut,
are similar. However, there are also some notable differences in their functioning.
Like most species of vertebrates, the birds secrete two peptide hormones from
their neurohypophysis (Table 4.1). Both of these differ in their structures from

Table 4.1. Neurohypophysial hormones in birds

Vasotocin Mesotocin* VIM ratio Vasotocin

mjlmolkg- 1 BW

Galliformes
Domestic fowl +' +' 6.7 1.2b
Domestic turkey" + + 1.2 0.2
Coturnix japonicad + + 4.2 Approx. 2
(Japanese quail)
Columbiformes
Columba liviab + + 7 0.4
(pigeon)
Anseriformes
Domestic duck' + +
Psittaciformes
Melopsittacus undulatu/ +
(budgerygah)
Charadriiformes
Larus canuss Pressor and oxytocic 8.6 9.5
(gull) activity
Passeriformes
Zonotrichia leucophrys gambeliih + + 3.5
(white-crowned sparrow)

* Originally identified as oxytocin, but now known to be mesotocin (Acher et al. 1970; Acher
1996).
' Munsick et al. (1960); Chauvet et al. (1960).
b Heller and Pickering (1961).
c Munsick (1964).
d Follett and Farner (1966).
' Hirano (1966).
r Hirano (1964).
8 C. Tyler quoted by Follett (1963).

h D. S. Farner and W. H. Sawyer; quoted by Sawyer (1968).

114
those present in most mammals, but they conform to the pattern of those secreted
by the other tetrapods. They are 8-arginine-vasotocin (vasotocin, AVT) and 8-
isoleucine-oxytocin (mesotocin, MT). Vasotocin functions as the antidiuretic
hormone in birds, where it replaces vasopressin. It differs from the latter by a
single amino acid substitution, isoleucine replacing phenylalanine at position 3
in the peptide. Mesotocin differs from mammalian oxytocin by the replacement
of leucine by isoleucine at position 8. (It will be recalled that mesotocin is also
present in some marsupials.) Mesotocin has negligible antidiuretic activity. Both
hormones can contract the bird oviduct, but vasotocin is more potent. Aphysio-
logical role for mesotocin has not been established in birds. Vasotocin is released
into the circulation of birds in response to hyperosmotic concentrations in the
plasma and also following stress, haemorrhage and during oviposition.
The principal secretions of adrenocortical tissue in birds are corticosterone and
aldosterone (Fig 2.1). Both of these hormones can influence salt metabolism, but
aldosterone is much more active. However, corticosterone is present at consider-
ably higher concentrations in the plasma and may also contribute to the regula-
tion of sodium and potassium in the body. The principal sites of such actions in
birds are the kidneys and the large intestine. Corticosterone is considered to prin-
cipally act as a glucocorticoid hormone and replaces cortisol, which usually reg-
ulates such functions in mammals. However, in some mammals, such as rats, mice
and rabbits, corticosterone is also the main glucocorticoid hormone. Aldosterone
and corticosterone are also the principal corticosteroid hormones in reptiles
and amphibians. Secretion of aldosterone into the blood usually occurs when
birds are provided with a diet that has a low content of sodium (Rice et al. 1985;
Rosenberg and Hurwitz 1987). The release of corticosterone can occur in condi-
tions that may result from stress. Some such circumstances may be related to
osmoregulation. Such a release occurs in ducks provided with an excess of salt in
their diet or in drinking water (Harvey et al. 1984; Klingbeil1885). Dehydration
also increases the release of corticosterone, as well as aldosterone, in ducks (Kling-
beil1985; Amason et al. 1986). Hormones that influence the synthesis of adreno-
corticosteroids appear, as in mammals, to include ACTH, angiotensin II and
natriuretic peptides. However, precise information of the relative importance and
respective roles of these hormones in regulating adrenocortical function in birds
is not available.
Birds possess a renin-angiotensin system. The juxtaglomerular apparatus ap-
pears to be similar to that in mammals. It includes granulated renin-secreting cells
and a macula densa. Renin promotes the formation of angiotensin, which can con-
tribute to the regulation of corticosteroid synthesis, blood pressure and thirst.
However, such functions have not been established in all the birds that
have been studied. For instance: angiotensin II can promote corticosteroid syn-
thesis in ducks, quail and turkeys, though apparently not in domestic fowl
(Holmes and Cronshaw 1993). The structures of renin and angiotensin in birds
differ from those in mammals. Renin from domestic fowl is specific to birds and
interacts only with avian plasma angiotensinogen to produce angiotensin I (Nolly
and Fasciola 1973). Angiotensin I in birds differs from that in mammals (cattle)
and reptiles (turtles and alligator) by a single amino acid substitution at position
9 {Fig. 2.6). However, avian angiotensin II has a structure identical to that in cattle

llS
and reptiles. Natriuretic peptides have been identified in birds. They include the
type-B (BNP-29) (Miyata et al. 1988) and type-C (CNP-22) peptides (Takei 1994).
As in mammals, they can inhibit the synthesis of aldosterone in birds (Gray et al.
1991).
Prolactin is released into the blood of birds in response to a hyperosmotic
plasma. However, a role for this hormone in avian osmoregulation is controver-
sial (Harvey et al. 1989). Avian prolactin differs in its structure from that of other
vertebrates, but when administered to other species it can still elicit characteris-
tic actions, such as the secretion of milk by mammary glands. In pigeons it stim-
ulates the secretion of "pigeon's milk" from the crop sac epithelium. In some fish,
prolactin can influence the movement of salt and water across various epithelia,
including the gills (see Chap. 7). Such observations appear to have encouraged a
search for analogous actions in the kidneys and gut of birds.

1 Water Loss

Water loss in birds takes place by evaporation, and in the urine, faeces and nasal
salt gland secretions (Maclean 1996). Increased amounts of water are also used
periodically for egg laying, and in some species can be disgorged from the crop
sac to feed the young. The contribution of each of these avenues to the total water
loss can vary, but principally depends on the prevailing climatic conditions. Evap-
orative water loss is usually predominant. It occurs from the respiratory tract and
the skin. Water loss in the urine and faeces may vary from the equivalent of 2 to
20% of the body weight each day. However, it usually represents about 5% of the
body weight in a day. Nasal salt gland secretion can be substantial, especially in
the marine birds. As these secretions have high osmotic concentrations, they
usually provide a net gain of water from imbibed salt solutions.
Few birds can survive indefinitely on a regimen of dry food, such as plant seeds,
with no water to drink. The water gained from the metabolism of such diets and
the small amounts of free water present usually do not compensate for other
losses. Under controlled laboratory conditions with moderate temperatures and
relative humidity, and freed from the need to actively search for food, budge-
rygahs and zebra finches have been observed to survive prolonged periods
without drinking water. However, under natural conditions, birds on such a
regimen progressively lose weight and eventually would die from dehydration.
California quail without water to drink die after losing about 50% of their body
weight, and the mourning dove after a loss of 37%. The house finch cannot survive
a loss exceeding 15% of its weight (Bartholomew and Cade 1963). The reasons for
such differences are not clear, but they may be related to the rates of dehydration.
The house finch loses water five-times as rapidly as the California quail and the
mourning dove at an intermediate rate. During dehydration, the haematocrit is
initially maintained at relatively constant levels in some birds, such as galahs
and feral chickens (Roberts 1991a,b ). This behaviour is reminiscent of that which
occurs in some desert mammals in which the blood volume is maintained at the
expense of intercellular and intracellular fluids.

116
 40r----------------------------------------------,

o---+- -Taeniopygia castanotis

Carpodacus mexicanus
o----Passer domesticus

.
Zonotrichia leucophrys
.--Pipilo maculatus

I~
~
Pipilo aber ti
Chordeiles acutipennis
Pholaenoptilus . nuttalli i
Pipilo fuscus
Lanius ludov1cianus Zenaidura macroura

·-
Richmondena cardinal is
imus polyg~ Toxostoma redivivum Lophortyx
---.:::;..__ _ _ _ e;;;Otus asio californicus

0 150
Fig.4.1. The relation of weight-relative evaporative water loss to body weight of birds at ambient
temperatures near 25 oc. The cross-hatched curve indicates the theoretical relation between body
weight and the production of metabolic water by birds in basal conditions utilizing exclusively
carbohydrates (upper boundary) or exclusively proteins (lower boundary). The values for fats
are intermediate. (Bartholomew and Cade 1963)

1.1 Evaporative

Evaporative water loss in birds is inversely related to their body weight (Fig. 4.1}.
This observation reflects their relative surface areas and rates of metabolism. This
water loss is increased at high body and environmental temperatures and when
the water vapour content of the air is low.
Water loss occurs from the respiratory tract as an unavoidable consequence of
the need to exchange oxygen and carbon dioxide. The body temperature of birds
is normally about 2 oc higher than that of most mammals (Prinzinger et al. 1991).
Their rates of metabolism are also usually higher. This avenue of water loss can
be substantial. Small birds, like small mammals, can utilize a countercurrent heat
exchanger in their nasal passages to cool expired air to a temperature that is less
than deep body temperature (Schmidt-Nielsen et al. 1970). The water losses in the
expired air are thus reduced, though the magnitude of the saving is not as great
in small birds as in mammals. Evaporation of water from the avian respiratory

117
tract, as in mammals, increases in response to homoiothermic need at elevated
ambient temperatures. This process can be seen to occur when the birds pant.
Birds can also accelerate movements of the hyoid apparatus in the throat to
promote evaporation. This activity is called gular flutter.
Birds lack sweat glands and so it was once thought that they lose little water
by evaporation from their skin. However, direct measurements of such water
loss from the skin of a variety of birds have shown that over 60% of their total
water loss can occur by this route (Bernstein 1971; Lasiewski et al. 1971). Such
cutaneous water loss can be regulated and increase in response to the need to
regulate the body temperature. Inhibition of the homoiothermic response of
the respiratory tract of mourning doves results in a rapid increase in cutaneous
evaporation (Hoffman and Walsberg 1999). Dehydration has been shown to
decrease evaporation from a number of birds, including the skin of zebra finches
(Lee and Schmidt-Nielsen 1971). The mechanisms involved in regulating such
changes in cutaneous evaporation are uncertain. In long-term hot conditions it
may involve changes in skin structure, such as the laying down oflipids that retard
water loss (Peltonen et al. 1998). Vascular changes could also be contributing. In
mammals, the circulation is under the control of the sympathetic nervous system
and a-adrenergic receptors, which mediate vasoconstriction. However, in heat-
acclimated pigeons the situation appears to be more complex and may involve
~-adrenergic receptors both peripherally and in the brain (Ophir et al. 2000).
Blockade of such receptors with drugs such as propranolol increases cutaneous
evaporation. The details of such a control system remain to be elucidated.
However, it may be relevant to observe that propranolol, via its ~ 1 -adrenergic
blocking effect, can prevent the activation of the renin-angiotensin system and
the formation of angiotensin II. This hormone has a powerful vasoconstrictor
action.
Evaporative water loss and metabolic rate in birds generally appear to be less
in species that live in deserts than those from more temperate regions {Tieleman
and Williams 2000). They reduce their evaporative water losses by utilizing a
number of strategies. Behavioural adjustments are very important (Davies 1982;
Dawson 1984). Most birds are diurnal in their activity so that under desert con-
ditions, in contrast to many mammals, they cannot avoid the heat of the day. In
such circumstances, birds may seek refuge in the shade of trees, bushes and rock
crevices. Very few birds are fossorial. Some birds avoid heat by soaring to heights
where the temperatures are lower. Some birds can enter states of torpor, but this
behaviour usually occurs under cold conditions when a conservation of energy
results. Corticosterone appears to be involved in the restoration of normal energy
metabolism following such torpor in humming birds (Hiebert et al. 2000). Under
hot conditions, birds may limit their activity and search for food to the cooler
hours in the early morning and late afternoon. To facilitate evaporative cooling
from the skin they can expose lightly feathered areas and spread their wings.
Non-evaporative heat exchanges involve conduction, radiation and convection.
The net flow of heat is from the hotter to the cooler region. As described ear-
lier, the body temperature of birds is generally somewhat higher than that of
mammals. Their lethal temperature is generally about 5 to 6 oc higher than the
normal body temperature. They can utilize this latitude for a controlled hyper-

118
thermia, which provides a strategy to delay the need for evaporative cooling
(Tieleman and Williams 1999). This process is most effective in small birds, when
savings of as much as 50% of their total evaporative water loss can occur. Such
birds, like mammals, may undergo alternate periods of nocturnal hypothermia
and hyperthermia in the daytime (King and Farner 1964). Flying in birds is asso-
ciated with considerable increases in metabolic rate and, potentially, evaporative
water loss. Budgerygahs flying in a wind tunnel at 20 oc have an evaporative water
loss which is five-times as great as at rest (Tucker 1968 ). At 36 oc, water loss during
flying was three-times as great as at 20°C. Water loss at the latter temperature was
equivalent to about 7% of their body weight each hour. Under natural conditions,
birds can make long, often uninterrupted flights, especially during periodic breed-
ing migrations. They apparently do not arrive at their destinations in a dehydrated
sate. Measurements of evaporative water loss in starlings flying in a wind tunnel
at different environmental temperatures indicate that radiation and convection
are the major mechanisms for heat loss during flying (Torre-Bueno 1978). By
ascending to higher altitudes, where the air is colder, birds can apparently main-
tain their hydration with water produced by the oxidation of body fat. It appears
that long-distance migrants fly at sufficiently high altitudes to dissipate heat prin-
cipally by convection.

1.2 Urinary and Faecal

Birds lack a urinary bladder, so that the urine and faeces are usually accumulated
together in the cloaca and rectum. Except in ostriches, in which the urine is stored
separately, the faeces and urine are voided at the same time. The composition of
the urine can be modified during such storage in the posterior large intestine as
a result of transmucosal movements of water and solutes. Due to their intermix-
ing separate measurements of urinary and faecal water and salt losses are usually
not feasible under natural conditions.
The excreta, urine plus faeces, of normally hydrated budgerygahs and zebra
finches contain about 80g water (lOOgt 1 wet weight. When drinking water is
restricted, this value decreases to nearly SOg (lOOgt 1 (Cade and Dybas 1962;
Calder 1964). In these birds, the total water loss each day in the urine and faeces
is about 2% of their body weight in a day. The water content of the excreta of other
birds has generally been found to be similar, though even lower concentrations
of water have sometimes been reported (Maclean 1996). Whether birds utilize
osmotic and hydraulic forces in the crypts of intestinal villi to dehydrate the
faeces, as occurs in mammals (see Chap. 1), is unknown.
Urinary water loss is influenced by the water and salt content of the diet, the
availability and composition of drinking water and the prevailing environmental
temperature and relative humidity. It may also be related to the concurrent activ-
ities of the gut and, if present, nasal salt glands. The volume of the urine will
depend on the amount of solutes to be excreted, including salts and uric acid, and
the state of the birds' hydration. Like mammals, birds can form a hyperosmotic
urine, but the concentrations that are achievable are usually not as great (Table

119
1.6). The urine/plasma concentration ratio usually does not exceed 2.5 (Poulsen
and Bartholomew 1962). However, there are exceptions, and in the savannah
sparrow this ratio can be 4 to 5 (about 2000 mosmoll- 1 ). This small bird lives in
salt marshes and can drink brackish water. The ability of birds to form hyperos-
motic urine reflects the presence of mammalian-type nephrons that form a coun-
tercurrent multiplier system (Poulsen 1965). However, these nephrons, which are
present in the renal medulla and have a loop of Henle, make up only about 20 to
30o/o of the total of those present in the bird kidney (Dantzler 1997). The remain-
ing cortical nephrons are smaller and lack a loop of Henle. They are described as
reptilian-type nephrons and do not contribute to the formation of the hyperos-
motic urine. Although they cannot usually concentrate their urine as much as
mammals, birds reduce their urinary water losses by excreting waste nitrogen as
uric acid. It has been estimated that 1 g of nitrogen then only requires 10 ml of
water for its excretion (Smith 1951). In contrast, a mammal, which utilizes urea,
would require as much as 50 ml of water for this excretion. The uric acid in the
urine forms smooth spheres that contain Ca2+ and K+. With the aid of proteins,
they form a colloidal suspension that exerts a negligible osmotic pressure while
maintaining the patency of the renal tubules (Braun 1999a). The protein present
in the urine, and much of the uric acid, is not excreted but reprocessed and
absorbed from the large intestine (see later).

1.3 Renal Water Conservation and the Neurohypophysis

The kidneys of birds adjust the volume and concentration of the urine in
response to their need to maintain normal bodily hydration. The administration
of water results in the formation of an appropriate volume of dilute urine. When
water is restricted, a smaller volume of more concentrated urine is formed. In
mammals, changes in the volume of the urine principally depend on regulating
the process of its reabsorption from the renal distal tubular-collecting duct
system. However, in birds, such renal conservation of water involves changes in
both the glomerular filtration rate (GFR) and tubular water reabsorption. This
involvement of glomerular filtration is similar to that which occurs in reptiles and
most other non-mammalian vertebrates. In birds, changes of the GFR involve
variations in the numbers of functioning glomeruli rather than the filtration
across individual, single, glomeruli. Such a process is called glomerular intermit-
tency or recruitment (Dantzler 1997). The reptilian-type nephrons are principally
involved in this process. When hyperosmotic saline is administered to desert
quail, the reptilian-type nephrons are completely closed down while the func-
tioning of the mammalian-type ones is little changed (Braun and Dantzler 1972).
Dehydration has been found to decrease the GFR in all birds that have been
studied. The inhibition varies from 20o/o in domestic fowl to 58o/o in starlings
(Roberts and Dantzler 1989). It is the predominant mechanism for antidiuresis in
desert-dwelling Gambel's quail (Williams et al. 199la).
Neurohypophysectomy in the domestic fowl results in the formation of large
volumes of dilute urine (Shirley and Nalbandov 1956). This condition of experi-

120
 mental diabetes insipidus is due to the lack of the avian antidiuretic hormone
vasotocin. In 1933 E. K. Marshall and his colleagues (Burgess et al. 1933) injected
commercial preparations of mammalian vasopressin (ADH, pitressin) into
domestic fowl and observed an antidiuretic response that was due to both an
increased reabsorption from the renal tubule and a decrease of the GFR. In 1960,
it was established that the antidiuretic hormone in birds was, in fact, vasotocin
and it elicited this same dual effect on the kidney (Munsick et al. 1960). Erik
Skadhauge in 1964 carefully analyzed the antidiuretic response to vasotocin in
the domestic fowl. He injected small doses of this hormone into the renal portal
veins so that only the tubules were exposed to effective concentrations of the
peptide. An antidiuretic effect was observed. Much larger doses of vasotocin were
required to promote the glomerular response. The administration of different
doses of vasotocin, over the physiological range, confirmed that in domestic fowl
the renal tubular response was the primary one (Stallone and Braun 1985).
However, in kelp gulls it has been observed that the glomerular response shows
a sensitivity to vasotocin similar to the tubular one (Gray and Erasmus 1988a).
These gulls live in coastal areas of South Africa where osmotic stresses are
expected to be greater than in domestic fowl, which originated in tropical jungles.
The greater emphasis on changes in the GFR in the gulls in response to vasotocin
may reflect an adaptation to more arid conditions. The glomerular response to
vasotocin is due to its vasoconstrictor effect on the afferent glomerular arteriole
(Braun 1976).
The role of vasotocin in regulating water excretion in birds was initially
inferred from changes in its storage in the neurohypophysis and the observed
antidiuretic effects of its administration in low doses. Giving pigeons 0.5 M
sodium chloride solutions to drink, or depriving Japanese quail of drinking water,
resulted in an 80 to 90% decline in the amounts of vasotocin stored in the neu-
rohypophysis (Ishii et al. 1962; Follett and Farner 1966). The presence of vaso-
tocin in the blood, at appropriate concentrations, was demonstrated only much
later, following the introduction of radioimmunoassays for the hormone. The
release of vasotocin into the blood of domestic fowl was shown to occur incre-
mentally over a range of changes in plasma osmotic pressure of physiological
magnitude (Stallone and Braun 1986a,b). In contrast to mammals, changes in
plasma volume, including haemorrhage, were much less effective stimuli for such
hormone release.
The changes in osmotic concentration in the plasma that promote release of
vasotocin have been compared in a number of birds. There are large differences
that appear to be related to the normal osmotic needs of the birds in their natural
habitats. The results have been summarized by Roberts (1991b) and are shown in
Table 4.2. The house sparrow displays the greatest osmotic sensitivity, releasing
vasotocin in response to the smallest change in the concentration of the plasma,
while the galah is the least sensitive. Feral "domestic" fowl living on an island off
the Australian coast were found to be more sensitive than their more domesti-
cated relatives. The galah is a parrot that is well adapted to life in the arid regions
of Australia. Possibly its needs for vasotocin have been reduced and the kidney
has evolved a greater sensitivity to this hormone. The concentration of vasotocin
in the plasma of pigeons has been measured following 5 h of continuous flight.

121
Table 4.2. Osmotic sensitivity of release of vasotocin (AVT) into
the plasma of birds

pg AVT ml- 1 per mosmol kg- 1

water increase in concentration

Domestic fowl" 0.5, 0.28

Feral domestic fowl' 1.75
Kelp gullb 1.13
Cape garnetb 0.36
Jackass penguinb 0.44
Pekin duck' 0.39
Galahd 0.16
House sparrow• 4.4
Ostrichr 0.54

• Roberts (l991b). b Gray and Erasmus (l988b). ' Gray and

Simon (1983). d Roberts (1991a). • Goldstein and Braun (1988)
calc by". r Gray et al. (1988).

They were found to increase to three to eight-times greater than those levels that
were present before the flight (Giladi et al. 1997). This change was accompanied
by a three-fold increase in urine concentration. The release of the hormone appar-
ently reflected the effects of exercise and dehydration.
The effect of vasotocin on the GFR in birds involves a constriction of the affer-
ent glomerular arteriole, but the nature of its action on the renal tubule is not
clear. Studies on the effects of synthetic analogues of vasotocin on the kidneys of
house sparrows indicate that the vascular effect is mediated by a V1-type recep-
tor (Goecke and Goldstein 1997). This receptor appears to be similar to the vas-
cular receptor utilized by vasopressin in mammals. However, the renal tubular
effect of vasotocin in birds does not appear to involve the mammalian-type V2
receptor that mediates a change in permeability to water. Indeed, a direct renal
tubular effect of vasotocin has been difficult to demonstrate in birds (Osono and
Nishimura 1994; Goldstein 1995; Nishimura et al. 1996). Based on experiments
using isolated renal tubules in Japanese quail, Nishimura and her collaborators
have suggested that the effect of vasotocin may be indirect. It could, for instance,
be due to a reduced delivery of fluid to the medullary collecting duct system.

2 Conservation and Excretion of Salts

The principal avenues for the excretion of salt in birds are the kidneys, gut and,
in some species, nasal salt glands. The amounts of Na+and K+ present in the urine
and faeces are mainly regulated by the adrenocortical steroids. Their synthesis is
controlled by ACTH, the renin-angiotensin system and, probably, natriuretic
peptides. The composition of the urine is further modified, again by adrenocor-
ticosteroids, after it has passed from the ureters into the cloaca. However, the

122
secretory activity by the nasal salt glands in birds, despite some early protesta-
tions, does not appear to be directly influenced by hormones. The parasympa-
thetic nervous system is the primary regulator of this process. The salt glands in
some birds may indirectly interact with the physiological activities of the kidneys
as salt-excreting organs. The diets and natural habitats of birds have a bearing on
the relative importance of these organs on the regulation of salt in the body. The
diet of seed-eating birds usually has a low content of Na+ and a high one of K+.
Carnivorous birds obtain adequate Na+in their food. The diet of marine and estu-
arine birds also contains adequate Na+ and may even provide an excess. Many
such species feed on invertebrates and even drink sea-water. These birds usually
utilize salt glands for the excretion of sodium chloride. Salt glands are also present
in a number of non-marine birds, especially carnivorous species. However, their
state of development varies and may not always be adequate to make a major con-
tribution to salt excretion.

2.1 Kidneys

As the ability of the kidneys in birds to form a hyperosmotic urine is not as great
as in mammals, their capacity to excrete excess salt by this route is somewhat
limited. However, as described earlier, some birds, such as the savannah sparrow,
can excrete sufficient amounts of salt in the urine to maintain osmotic balance
on diets containing relatively large quantities of salt. The sodium chloride content
of the urine of birds on low-salt diets indicates that concentrations as low as 5
mmoll- 1 are attained. Indirect estimates of tubular reabsorption, involving mea-
surements of the rates of glomerular filtration of solutes into the nephron and the
amounts excreted in the urine, indicate the presence of a highly efficient reab-
sorptive process for salts and water. These processes include tubular absorption
and secretion of K+. Direct measurements of such tubular processes involving the
collection of fluid in micropipettes and the perfusion of selected segments of the
nephron are not widely available in birds. However, the available information indi-
cates that the mammalian pattern of salt and water reabsorption in the proximal
tubule, followed by a more selective modification of the filtrate in the distal tubule,
also appears to be present in birds (Laverty 1989; Osono and Nishimura 1994;
Nishimura et al. 1996). Nevertheless, there are some differences, such as involve
the mechanism of action of vasotocin on water reabsorption (see above).
Adrenalectomy in ducks results in an excessive loss of Na+ in the urine that
reflects a deficiency of adrenocorticosteroids (Thomas and Phillips 1975). Normal
function can be restored by the administration of these hormones. Similar effects
of adrenalectomy have been observed in domestic fowl and pigeons (Parkins
1931; Miller and Riddle 1942). Aldosterone is the most active mineralocorticoid
hormone in birds, but corticosterone also can exhibit substantial such activity.
However, in domestic fowl, the former steroid is released more predictably in
response to a depletion of body sodium (Rice et al.1985; Rosenberg and Hurwitz
1987). Aldosterone, as well as corticosterone, has been observed directly, in vitro,

123
to stimulate Na+transport across the large intestine of domestic fowl (see below).
It seems likely that it is exerting a similar effect on the renal tubule. Aldosterone
also promotes K+ secretion in the urine of mammals, but such an effect has not
been clearly demonstrated in birds (Simon and Gray 1991).
The infusion of isosmotic sodium chloride solutions into birds evokes a diure-
sis. In domestic fowl and ducks, this effect appears to be mediated by atrial
natriuretic peptide. This hormone promotes an increased GFR and a decreased
reabsorption ofNa+from the distal renal tubule (Gray 1993, 1994). The latter effect
appears to reflect a reduced synthesis of aldosterone, as observed in mammals,
but a direct inhibition of Na+ transport could also be occurring (Rosenberg et al.
1988).

2.2 Nasal Salt Glands

Excessive accumulations of sodium chloride are excreted solely by the kidneys of

many birds. However, some species also utilize nasal salt glands for such excre-
tion. Their secretions usually contain sodium chloride at far higher concentra-
tions than are present in the urine (Table 1.5}. (Avian salt glands, in contrast to
those of some reptiles, do not appear to contribute significantly to K+ excretion.)
Concurrent water loss is accordingly much less than that in urine. Many marine
and estuarine birds can subsist on a high salt diet and even fruitfully drink sea-
water by utilizing nasal salt glands for such excretion. These glands have been
mainly studied in marine birds, but they have also been identified in many car-
nivorous species, especially Falconiformes, including hawks, eagles and vultures
(Cade and Greenwald 1966}. They are also present in the roadrunner, Geococcys
californianus, which is carnivorous and lives in desert areas of the southwest USA.
However, the nasal salt glands in such birds do not always appear to be in a highly
functional condition. It has been suggested that their activity may be more impor-
tant in their relatively immobile exposed nestlings than in the adults (Ohmart
1972}. Nasal salt glands do not appear to be present in the Passeriformes (perch-
ing birds). Laboratory investigations have mainly utilized gulls, Pekin ducks and
geese. The functioning of these glands was first described by Knut Schmidt-
Nielsen and his colleagues in 1958. They studied cormorants, brown pelicans and
herring gulls (Schmidt-Nielsen and Hinge 1958; Schmidt-Nielsen et al. 1958;
Hinge et al. 1958}. The administration of hyperosmotic solutions of sodium chlo-
ride rapidly evoked a voluminous secretion from the nasal glands of these birds.
Hyperosmotic sucrose, but not urea or glucose, was also effective, suggesting that
the response involved osmoreceptors. Such receptors have been identified in the
hypothalamus (Gerstberger et al. 1984}. Whether or not volume receptors that
respond to an expansion of the extracellular fluid space are also involved has
been controversial. A response to the infusion of isosmotic solutions has been
described in Pekin ducks and Elder ducks (Hammel et al. 1980; B0keness and
Mercer 1995; Bennett et al. 1997}. Volume receptors appear to be present in the
heart or are associated with the large blood vessels. However, the response to
extracellular volume expansion is not as great as that to osmotic stimuli. It may

124
even be an indirect effect due to a lowering of the threshold for the stimulation
of the osmoreceptors.
Secretion by nasal salt glands in birds can be abolished by severing their
parasympathetic nerve supply (Schmidt-Nielsen 1960). Pharmacological block-
ade can also be achieved by administering atropine, which blocks acetylcholine
(muscarinic) receptors at the nerve junctions. General anaesthesia also inhibits
secretion. The secretory process appears to be initiated in the brain in the region
of the hypothalamus. It is accompanied by a large increase in the blood flow to
the nasal gland. The administration of adrenaline inhibits secretion, apparently
by its vasoconstrictor action.
Vasoactive intestinal peptide (VIP) is a neuropeptide that was first identified
in the gut of mammals. It has since been found in association with other neuro-
transmitters at many nerve endings. VIP has been identified in the terminals of
the parasympathetic nerves supplying the salt glands of Pekin ducks (Lowy et al.
1987). The infusion of VIP into these ducks can induce secretion from the nasal
glands. Normally, VIP appears to be released, concurrently with acetylcholine,
from the nerves supplying the salt glands. It may act by enhancing the local blood
supply and even potentiate the response to acetylcholine (Shuttleworth and Hilde-
brandt 1999).
Hormones do not appear to have a direct role in the functioning of the nasal
salt glands in birds. However, experimental manipulation of the endocrine system
and the administration of some hormones can influence their secretion. Such
effects have generally been described as indirect, secondary or modulating (Butler
et al. 1989; Shuttleworth and Hildebrandt 1999). Adrenalectomy in ducks was
found to inhibit the responsiveness of the salt glands, and their function could be
restored by the administration of corticosterone. However, this hormone defi-
ciency appears to result in a general debilitation of the birds and the blood supply
to the salt glands. The administration of vasotocin is without effect on secretion,
and a possible action of prolactin is considered to be of doubtful significance. The
injection of angiotensin II into Pekin ducks and kelp gulls inhibits salt gland
secretion (Hammel and Maggert 1983; Wilson et al. 1985; Gray and Erasmus
1989a). This effect appears to be mediated in the hypothalamus as it is not seen
following direct stimulation of the gland with methacholine (an analogue of
acetylcholine) (Butler 1999). Whether angiotensin II has a physiological role in
modulating the initiation of the secretion of the salt glands remains to be estab-
lished. Binding sites, possibly receptors, for melatonin (normally secreted by the
pineal gland) have been identified in the salt glands of Pekin ducks (Ching et al.
1999). The infusion of melatonin delays the secretory response and decreases its
rate. The administration of atrial natriuretic peptide into ducks has been shown
to increase secretion from the salt glands (Schutz and Gerstberger 1990). Specific
binding sites (receptors?) for ANP have also been identified in this gland. It was
suggested the ANP acts as an "emergency hormone" and may facilitate secretion
following a rapid expansion of the extracellular fluid space.
The size of nasal salt glands appears to be related to the feeding habits of some
birds. If young gulls, Larus glaucescens, and ducklings are provided with salt solu-
tions to drink, the salt glands enlarge compared to birds provided with fresh water
(Holmes et al. 1961; Schmidt-Nielsen and Kim 1964). Birds that inhabit marine

125
environments also have larger salt glands than those species that habitually drink
fresh water (Technau 1936). The increase in the size of the salt glands of eider
ducks adapted to drinking sea-water has been shown to be due to an increase in
the size, but not the number, of the cells (B0kenes and Mercer 1998). This hyper-
trophic response, like secretion, is initiated by stimulation of the parasympathetic
nerve supply to the gland (Shuttleworth and Hildebrandt 1999). Local growth
factors could ultimately be involved in this response.

3 Conservation of Water and Salt by the Cloaca and Large Intestine

Birds possess a cloaca consisting of three chambers, the proctodaeum, urodaeum

and coprodaeum. The ureters usually open into the urodaeum. (In ostriches they
open into the coprodaeum.) The large intestine, or colon, opens into the copro-
daeum. One or two caecae open into the large intestine of many birds. This occurs
at its junction with the small intestine. These "rectal caecae" are blind sacs, which
are lined by intestinal mucosa cells. They are often quite large in herbivorous and
omnivorous birds, but may be small, vestigial or absent in carnivorous and some
granivorous species, such as the budgerygah. Morphologically, these caecae are
considered to be part of the large intestine. The organ complex of the large intes-
tine and cloaca is often referred to as the lower intestine. It provides a fermenta-
tive chamber for nutrients and the recycling of nitrogen derived from urinary
uric acid and protein (Braun 1999b). The contents of the lower intestine can be
mixed longitudinally so that urine may pass in a retrograde direction, by reverse
peristalsis, into the caecae. This process appears to be influenced by the concen-
tration of the urine and could involve neural, and even hormonally controlled,
mechanisms. This passage of urine into the large intestine was first observed in
the domestic fowl using radiographic contrast media and X-ray examination
(Akester et al. 1967; Nechay et al. 1968). Skadhauge (1968) observed traces of uric
acid, from the urine, far up into the large intestine and caecae of domestic fowl
and ducks.
The possibility that changes in the water and salt content of the urine may take
place after it passes into the cloaca was first investigated in domestic fowl in 1942
by Hart and Essex. They found that surgical transplantation of the ureters to the
exterior, thus bypassing the cloaca, resulted in an additional dietary need for salt.
Dicker and Haslam in 1966 also demonstrated that such birds drank twice the
quantity of water as normal ones. These observations suggested that additional
losses of salt and water were occurring following the surgical by-passing of the
cloaca. This loss could be due to a failure in their reabsorption from the cloaca
and large intestine. A reabsorption of sodium and water has since been demon-
strated both in vivo and in vitro from the coprodaeum, large intestine and caecae.
Such observations have been made on domestic fowl and a variety of more exotic
birds (Skadhauge 1967; Bindslev and Skadhauge 1971; Chosniak et al. 1977;
Thomas et al. 1980; Rice and Skadhauge 1982; Laverty and Skadhauge 1999). The
lower intestine of birds has been described as an integrator of renal and intesti-
nal excretion (Thomas 1982; Braun 1999b). In domestic fowl, the caecae make the

126
greatest contribution to the reabsorption process, followed by the large intestine
and then the coprodaeum.
Reabsorption of Na+ from the avian lower intestine occurs as a result of its
active transepithelial transport. An electrical potential difference (PD), lumen
usually electronegative, and transmural solute concentration gradients are gen-
erated by this process. The latter can influence osmotic movements of water while
the PD can affect the movements of other ions, including Cl- and K+. At least two
active Na+ transport mechanisms have been identified in the avian lower intes-
tine. There is a linked cotransport of either amino acids, glucose or acetate to Na+.
There is also an amiloride-inhibitable transport involving specialized epithelial
sodium channels (ENaC). The latter process can be increased, as in many other
tetrapod vertebrates, by aldosterone (Thomas and Skadhauge 1979; Thomas et al.
1980; Grubb and Bentley 1987, 1992). Adiet with a low content of sodium also
increases such Na+ transport in the domestic fowl. As described earlier, such a
regimen is known to increase the secretion of aldosterone in these birds. Aldos-
terone has also been shown to stimulate the secretion of K+ by the large intestine
of the domestic fowl (Thomas and Skadhauge 1979, 1988, 1989).
The possible actions of other hormones on ion and water movements across
the avian large intestine have also been investigated (Laverty and Skadhauge
1999). Vasotocin has no effect on osmotic water transfer (Skadhauge 1967).
Ovine prolactin has been shown, in vitro, to decrease Na+ and water absorption
from the large intestine of the domestic fowl (Morley et al. 1981). This hormone
is released in response to dehydration in these birds (Amason et al. 1986). A
possible physiological role for such an effect of this hormone has not been
established. Corticosterone is normally present in the plasma of domestic fowl
in concentrations which, in vitro, are sufficient to stimulate Na+ transport across
the caecum (Grubb and Bentley 1992). However, it is possible that its local
concentration, in vivo, in the region of its effectors is reduced by 11~-hydro­
xysteroid dehydrogenase. Aldosterone is not inactivated by this enzyme so that
its effect would then be expected to predominate. Thus, in mammals its contri-
bution to a specific mineralocorticoid-mediated effects is unaffected. It is possi-
ble that corticosterone contributes to the maintenance of basal levels of Na+
transport in such avian tissues (Grubb and Bentley 1989; Amason and Skadhauge
1991).
The functioning of the cloaca and large intestine of birds may be integrated
with that of the nasal salt glands (Schmidt-Nielsen et al. 1963). Birds can secrete
sodium chloride from the salt glands in much higher concentrations than those
in the urine. Salt in the urine may be reabsorbed from the lower intestine and
be subsequently secreted as a more concentrated solution by the salt glands.
However, attempts to confirm this ingenious hypothesis by direct measurements
has yielded conflicting results (Goldstein et al. 1986; Thomas 1997; Hughes et al.
1999). Such a recycling of salt and water could be occurring in some birds.
It is interesting to observe that ligation of the caecae in ducks undergoing
acclimation to drinking sea-water results in a decrease in the size of their salt
glands (Hughes et al. 1992). It appears that they do not then detect or respond
to the additional salt in their diets. A more direct interaction of salt gland and
kidney function could also arise from a controlled increase in the renal tubular

127
absorption of excess salt. This salt may then be preferentially excreted by the salt
glands.

4 Sources of Water and Salts

4.1 Food

Salts and water are obtained from the food of birds. The adequacy or excess of
such accumulation will depend on the diet. A succulent herbivorous diet may
supply a bird with all the water and salts it needs. However, in some geographic
areas, the sodium content of such vegetation may be low. Halophytic plants are
common in some areas, but their contribution to the diets of birds does not
appear to have been recorded. Nectarivorous birds usually have an excess of water,
which can result in a persistent diuresis. Avian carnivores and insectivores gen-
erally obtain adequate salts and water from their food. However, many birds,
including species that live in dry desert regions, subsist on air-dried seeds. This
food contains little sodium and only about 10% preformed water. Water formed
by the oxidation of fats, carbohydrates and proteins (metabolic water) makes an
important contribution to the needs of granivorous birds. Birds gain a little more
water than mammals from the oxidation of proteins. This difference reflects the
ultimate formation of uric acid instead of urea. Birds produce 0.499 g water g- 1
protein oxidized compared to 0.396 g water g- 1 protein in mammals. Cade and
Dybas (1962) have calculated that commercial birdseed yields water of oxidation
that is equivalent to 45% of its weight. Estimates are similar for the seeds that
birds eat in the wild. However, even under temperate conditions, this water is inad-
equate for the bird's normal needs. Some birds exhibit signs of an enhanced salt
appetite and actively seek sources of salt. The red crossbill, Loxia curvirostra, has
even been observed to eat rock salt (Dawson and Shoemaker 1965).

4.2 Drinking

Many birds, especially granivorous species, depend on the availability of drink-

ing water to maintain adequate bodily hydration. This need is inversely related to
their body weight and is greatest in hot dry conditions and following flight, espe-
cially at low altitudes. In some instances, the amount of water required may be
equivalent to 100% of their body weight each day (Bartholomew and Cade 1963).
Drinking may be sporadic, but birds often exhibit regular patterns of drinking
behaviour. In deserts they may frequent water holes only during the cooler early
morning and evening hours (Fisher et al. 1972; Maclean 1996). Some birds drink
large volumes of water rapidly, even, as observed in budgerygahs, "on the wing".
Such behaviour appears to reduce the risk of predation. Birds often utilize their
natural aerial ability to travel long distances to drink (Dawson 1984). Sandgrouse
have been observed to travel 50 km to water. Young ostriches can store substan-

128
tial volumes of water in their glandular stomach (Degen et al. 1994). This allows
them to drink only once a day. Ostriches usually range within 20 to 30 km of water,
but they have been observed 80 km away.
Sea birds, such as albatross, cormorants, penguins and gulls, drink sea-water
and utilize their nasal salt glands for the excretion of the excess salt. Some
terrestrial birds have brackish water available, and this can occur in desert
environments and salt marshes (Maclean 1996). As such birds usually lack func-
tional salt glands and have a limited ability to concentrate the urine, the accept-
able concentrations of salt in such drinking water is usually less than 300 mmol
l- 1 (=50% sea-water). Given a choice of fresh or salt water, few birds will drink
solutions with a greater concentration than 100mmoll- 1 (Robinson et al. 1980).
Sometimes, under stringent laboratory conditions, zebra finches and savannah
sparrows can be persuaded to drink solutions approaching the concentration of
sea-water.
A decrease in the extracellular fluid volume, such as occurs during dehydra-
tion, results in hypovolemic thirst. As described in Chapter 1, this behaviour
results from an activation of the renin-angiotensin system and the formation of
angiotensin II. This hormone acts in the hypothalamus to induce drinking behav-
iour in many vertebrates, including birds (Kobayashi and Takei 1982, 1997). Dehy-
dration has been shown to increase the concentration of this hormone in the
plasma of various avian species, including Japanese quail (Okawara et al. 1985),
ducks (Gray and Simon 1987),ostriches (Grayet al.1988) and several marine birds
(Gray and Erasmus 1988b). Some birds, especially omnivorous and granivorous
species, readily exhibit drinking behaviour in response to the administration of
low doses of angiotensin II. Carnivorous birds are generally less sensitive. Birds
that have evolved in dry desert conditions are also generally less responsive to the
administration of angiotensin II (Kobayashi 1981; Kobayashi and Takei 1997).
Three species of Australian parrots belonging to the genus Barnadius display such
differences in sensitivity to this hormone. The twenty-eight parrot lives in tem-
perate areas, while the Port Lincoln parrot occupies arid regions. However, it is
considered to have only recently evolved from a temperate-living ancestor. Both
of these parrots readily drink in response to administered angiotensin II. In con-
trast, the mallee ringneck parrot, which evolved long ago in desert areas, does not
exhibit drinking behaviour in response to angiotensin II. Possibly the threshold
for the activation of this thirst mechanism has increased in the desert species.
Such a change could result in a less incessant thirst sensation and greater inter-
vals between periodic drinks.
The antidiuretic hormones, vasopressin in mammals and vasotocin in birds,
are released in response to dehydration. The possibility that they may exhibit
dipsogenic effects is controversial (Fitzsimons 1998). In ducks, angiotensin-like
responsive neurons in the hypothalamus can be stimulated, in vitro, by vasotocin
(Schmid and Simon 1996). However, such an effect is apparent only with high,
non-physiological, concentrations of this hormone. The stimulation of salt
appetite in mammals can involve interactions between angiotensin II, ACTH and
adrenocortical steroids (see Chap. 2). Asynergistic effect between angiotensin II
and mineralocorticoids in promoting salt appetite has been described in pigeons
(Massi and Epstein 1990).

129
S Reproduction, Migration and Osmoregulation

Reproduction results in an increased need for water and salts in birds as a result
of their increased activity, the production of eggs and, in many instances, the
nurture of the young. The timing of reproduction in birds is well coordinated
and usually involves responses to changes in the length of the daylight hours.
Such photoperiodic cues are received and interpreted by the hypothalamus.
A secretion of gonadotropin-releasing hormone (GnRH) takes place, resulting
in the release of gonadotropins from the pituitary gland. The latter hormones
promote the development of the gonads that secrete androgens and estrogens.
Birds usually breed in spring in response to increases in day length, but some
respond to shortening of the days and reproduce later in the year. Such times are
predicted to be those that are the most favourable for the survival of the young.
Breeding may be preceded by the migration of birds to areas where favourable
conditions are likely to occur. Such migration may be transcontinental and even
transhemispheric.
Bird migration involves the actions of various hormones, but their possible
roles as initiators of these events are not clear (Biebach 1990; Wingfield et al.
1990). Preparations for migration include increased feeding activity and
the storage of body fat, which may increase from normal values of 2 to 10% of
the body weight to 50%. Apart from supplying energy for such flights, this fat
also indirectly provides water storage. Yapp (1956) considered that water loss is
the greatest single limiting factor in bird migration. However, long-distance
avian migrants do not usually arrive at their destinations in seriously dehydrated
condition. Providing that they fly at altitudes where the temperature does not
exceed 7 to 10 °C, they appear to be able to exist on the water provided by the
oxidation of the fat that they metabolize (Torre-Bueno 1978; Biebach 1990).
This strategy is not feasible for all birds, such as those that fly at lower altitudes.
However, it has been calculated (Tucker 1968) that a budgerygah can fly for
at least 500 km without becoming seriously dehydrated. Even with fat storage
equivalent to 4% of their body weight, they possibly could fly non-stop, under
natural conditions, for about lOOkm (Wyndham 1980). Vasotocin levels in
the plasma have been shown to increase markedly in pigeons following
flight (Giladi et al. 1997). This hormone could be contributing to the water
conservation of birds on such occasions. Corticosterone and growth hormone
levels in the plasma were found to be elevated during a stopover in the autumnal
migration of sonderlings and semipalmated sandpipers in Delaware Bay in
the USA (Tsipoura et al. 1999). The corticosterone concentrations could be
reflecting stress. The elevated growth hormone levels may be the result of
rapid lipolysis during the flight. Corticosterone has also been measured in the
plasma of garden warblers during a stopover in the Sahara Desert in Algeria
(Schwabl et al. 1991). It was found to be low and inversely related to the remain-
ing fat stores.
Deserts provide relatively unpredictable habitats for successful breeding due
to the hot dry conditions and the sporadic nature of the rainfall. In the Southern
Hemisphere, especially in the central and western Australian deserts, photo-
periodic cues for breeding appear to have been replaced by signals related to rain-

130
fall (Marshall 1961; Immelman 1971; Serventy 1971; Maclean 1996). Courting
behaviour can commence within minutes of rain falling in such areas and copu-
lation may occur 2 h later. Such "opportunistic" breeding may also occur in
response to the associated increases in food supply, humidity and even the green
colour of the vegetation. Such birds appear to maintain a tonic pituitary
gonadotropic activity which, when further activated, results in a rapid recrudes-
cence of the gonads. Rainfall in such areas can result in the immigration of
nomadic species and even water birds. Birds living in the deserts of the Northern
Hemisphere, such as the Sonoran Desert in the USA, appear to still utilize pho-
toperiodic signals to control the time of their breeding. However, their behaviour
at this time may be modified in response to a limited water supply (Vleck 1993).
Thus, drought and dehydration can suppress reproductive activity (Cain and Lien
1985; Vleck and Priedkalns 1985; Wingfield et al. 1992). It is possible that this
response is mediate·d by increased secretion of corticosterone.
The clutch size in desert birds is usually smaller than that in species that live
in temperate regions. This may reflect a more tentative investment in reproduc-
tory success. The eggs often hatch asynchronously, which facilitates a reduction
in the brood size in times of nutritional hardship. The older, larger nestlings can
then more readily engage in siblicide. If conditions are favourable, the breeding
season may be extended so that as many as four successive broods are produced.
Sexual maturity is often achieved rapidly so that the earliest chicks may breed
towards the end of the same season. The sexes of desert birds frequently exhibit
cooperative behaviour to assure the survival of the eggs and young. They are also
often monogamous.
Desert birds exhibit some interesting adaptations related to the survival of
the eggs and young in hot dry conditions. Some birds, such as sandgrouse and
emus, incubate the eggs in exposed situations. They protect them from overheat-
ing by raising the feathers, thus increasing the insulation and providing an
enveloping heat sink. The male emu incubates the eggs. He has a reduced
metabolism and loses less than 50% as much water by evaporation as non-
incubating dehydrated emus (Buttemer and Dawson 1989). The physiological
basis for this effect is unknown, but could possibly involve a depression of thyroid
gland function. Many birds feed their young with food that has been moistened
in the crop. As described earlier, columbiforme birds can, under the influence of
prolactin, secrete "milk" from the crop sac with which they feed their young.
Male sandgrouse (genus Pterocles) that live in deserts in Africa and the
Middle East have a remarkable way of collecting water for the young (Cade
and Maclean 1967; Thomas and Robin 1977). In 1896, the British aviculturist E.
G. B. Meade-Waldo (quoted by Cade and Maclean 1967) observed these birds
saturating their breast feathers with water while they were drinking. On return-
ing to the nest the young imbibe this water by "stripping" it from the feathers.
The feathers have a special design enabling their rapid hydration and the
ability to hold large amounts of water. Possibly angiotensin II promotes such
stripping?

131
6 Osmoregulation and Hormones in Free-Living Birds

The observations that have been described in this chapter were usually made on
domestic or captive wild birds maintained under laboratory conditions. The
experiments were often performed in vitro, or in vivo using anaesthetized and
restrained birds. Normal physiological processes can only be inferred from such
experiments. Observations on free-living wild birds may be illuminating, but are
few in number. Exchanges, or turnover, of body water and salts can sometimes be
measured in free-living birds with the aid of radioisotopes. Implanted devices,
such as miniosmotic pumps, can be used to measure the GFR. Following
"non-stressful" apprehension, samples of tissue can be promptly collected and
analyzed. The results of a variety of such observations and their ecological sig-
nificance have been reviewed by Goldstein (1997) and Thomas (1997).
Plasma concentrations of aldosterone from wild house sparrows collected in
Ohio were found to be similar to those of captive birds maintained on a diet which
had a low sodium content (Goldstein 1993). The plasma concentrations of vaso-
tocin, aldosterone and the turnover of body water and sodium have been mea-
sured in five species of Australian honeyeaters (family Meliphagidae) (Goldstein
and Bradshaw 1998). These birds live in a variety of geographic areas. Quantita-
tive differences between the values of such physiological measurements could be
related to their natural diets, the season, body size and habitat. Measurements of
the body water turnover, haematocrit, and plasma osmolality and corticosterone
concentration have been made in a small passerine, the silver eye, Zosterops lat-
eralis (Rooke et al. 1983, 1986). This bird lives in a temperate but seasonally vari-
able region in south Western Australia. The measurements indicated that the birds
experienced dehydration in summer and potentially fatal stressful conditions in
late summer and early winter. Similar measurements were made to define the sea-
sonal physiological condition of a free-ranging subspecies of scrub wrens, Seri-
cornis frontalis (family Acanthizidae) (Ambrose and Bradshaw 1988). These birds
occupy arid, semiarid and temperate environments in Western Australia and were
found to experience different levels of osmotic stress related to their natural envi-
ronments. Extrarenal water loss has been compared in several species of wild
Australian parrots (Williams et al. 1991b). Water loss was lowest in the desert-
adapted species. Recently captured wild emus have provided in vitro preparations
of the lower intestine for the study of its ability to actively transport Na+ (Skad-
hauge et al. 1991). Measurement of transmucosal electrical parameters, such as
the potential difference, in this preparation indicated that it had a high capacity
for active Na+ transport. As this process could be inhibited by the drug amiloride,
it probably is under the control of aldosterone. The lower intestine could be
playing an important role in the adaptation of these birds to their life in arid
conditions. Other observations have been made in wild birds, especially in
species living in the deserts of the USA, Africa and the Middle East. However,
there are few direct measurements of the hormones that contribute to their
osmoregulation.

132
Chapter 5

The Reptiles

Reptiles are considered phyletically to represent the first truly terrestrial verte-
brates. They originated in the early Mesozoic period from an amphibian-like
ancestor. In those times they became the predominant tetrapod vertebrates, living
not only on the dry land, but also in the fresh water of lakes and rivers, and in the
sea. Four principal groups of reptiles have persisted to the present day. The Che-
lonia (turtles and tortoises) have changed little since their origin in early Trias-
sic times and today are represented by about 50 genera. These reptiles have a
worldwide distribution; they are usually aquatic (or more strictly amphibious) in
their habits. Five species live in the sea, although they must return to dry land in
order to lay their eggs. Anumber of chelonians have adopted a life in arid desert
regions, and these include the North American desert tortoise, Gopherus agassizii,
and the Mediterranean tortoise, Testudo graeca. The Crocodilia (nine genera)
have existed in a relatively unchanged form since they first appeared in the late
Triassic period. They are mostly aquatic, living in the vicinity of fresh water, but
at least one species, Crocodilus porosus, ventures into the sea for periods of uncer-
tain duration. The Squamata, numerically the principal contemporary reptiles,
consist of two main groups; the Lacertilia (lizards) and Ophidia (snakes), which
originated in the Jurassic and Cretaceous periods, respectively. Today, they are
each represented by about 300 genera. The lizards have the widest geographic dis-
tribution of the reptiles and are even found on many oceanic islands. The marine
iguana of the Galapagos islands, Amblyrhynchus cristatus, spends much of its time
feeding on the algae in the sea. The snakes also have a wide distribution and one
family, the Hydrophiidae {15 genera), lives principally in the sea. Terrestrial
snakes and lizards live in habitats ranging from tropical rainforests to dry desert
regions. The remaining major group is the Rhynchocephalia, a relict branch of
the reptiles with one surviving species, Sphenodon (the tuatara), which is now
confined to a wet temperate environment on a few small islands situated off the
coast of New Zealand.
Compared with their amphibian ancestors, reptiles are considered to be
relatively independent of the proximity of fresh water. Many species, however,
continue to live in the vicinity of lakes and rivers, though, unlike almost all
amphibians, they produce an egg that, by virtue of its shell and amnionic mem-
brane, can be laid on land. Some of the sea snakes, Pelamis, however, do not even
need to return to land for this purpose, as they give birth to live young in the sea.
As compared to the amphibians, the reptiles have a relatively impermeable skin
which limits exchanges of their water and salts with the environment. Many
reptiles, especially those living in arid areas, can form uric acid (instead of urea
or ammonia) as the principal end product of nitrogen metabolism, so that they

133
require little water for the renal excretion of catabolic nitrogen. The three afore-
mentioned factors, amniotic egg, relatively impermeable integument and uri-
cotelism, distinguish the reptiles osmotically from their ancestral amphibian
forms, and must contribute substantially to the cosmopolitan radiation of this
group into regions of potential osmotic hostility.
The geographic dispersion of many terrestrial species across large expanses of
the oceans is often difficult to envisage, but this has undoubtedly occurred among
the reptiles (Darlington 1957), a feat that must largely reflect their relative osmotic
independence from their environment. Reptiles are thought to have originated in
the Old World and migrated to the New World, with a subsequent pilgrimage from
South America to Australia. Darlington states that these movements can be
explained "without resorting to special land bridges or continental drift", pre-
sumably by making transoceanic voyages. Fossil representatives of an extinct
group of land tortoises (Meiolaniidae) from South America have been found on
Lord Howe Island and Walpole Island in the eastern Pacific Ocean. It seems likely
that these reptiles floated or possibly "rafted", across the many hundreds of kilo-
metres of ocean to occupy these remote islands. Turtles have a remarkable
propensity to survive such conditions. Among the snakes, the genus Natrix has a
remarkably wide geographic distribution and is found in Europe, Asia, Africa,
Australia, America and islands such as Cuba and Madagascar. These snakes are
primarily aquatic, but have probably attained their cosmoplitan status by cross-
ing the seas. Pettus (1958) compared the fluid metabolism of two races of Natrix
sipedon living in the southern United States. One of these groups normally lives
in fresh water and the other in brackish water; but the former cannot usually
survive transfer to a saline medium. The success of such adaptation seems to
reside solely in a predisposition to refrain from drinking salt solutions. Provid-
ing that reptiles maintain the relative impermeability of their integument, dis-
persal of terrestrial species through the seas is physiologically conceivable.
The reptiles utilize the same complement of hormones for their osmoregula-
tion as their amphibian progenitors and the birds that evolved from them. Some
differences in the precise structures of these hormones have emerged and a few
of their physiological actions may differ. The neurohypophysis of reptiles, like that
of other nonmammalian tetrapods, stores and secretes 8-arginine vasotocin (AVT,
vasotocin) and mesotocin (Table 5.1). The former peptide functions as an antid-
iuretic hormone, as occurs in birds and the amphibians. The principal hormones
secreted by adrenocortical tissue in reptiles are aldosterone and corticosterone
(Table 5.2), which is also similar to the pattern in the latter two groups of
tetrapods. The actions of these steroidal hormones are not as well defined as in
birds, but they also appear to contribute to the regulation of sodium and, pos-
sibly, potassium metabolism. The activity of adrenocortical tissue in reptiles, like
that in most other vertebrates, is regulated by ACTH and the renin-angiotensin
system. However, the evidence for such effects is somewhat fragmentary in the
reptiles. Removal of segments of the adenohypophysis of the chameleon lizard,
Anolis carolinensis, resulted in the disappearance of corticosterone from the
plasma (Licht and Bradshaw 1969). Conversely, the administration of mammalian
ACTH and extracts of the adenohypophyses of various reptiles increased plasma
corticosterone concentrations. Renin-like activity has been identified in the

134
Table 5.1. Distribution of neurohypophysial hormones in reptiles

Vasotocin Mesotocin

Crocodilia
Caiman (Caiman sclerops )a +
Chelonia
Mediterranean tortoise (Testudo graeca)b + +*
Green sea turtle (Chelonia mydas)a,c + +*
Slider turtle (Pseudemys scripta)d +
Ridley turtle (Lepidochelys kempi)' + +*
Loggerhead turtle (Caretta sp. )' + +*
Lacertilia
Green iguana (Iguana iguana)' + +
Ophidia
Grass snake (Tropidonotus natrix)b,c + +*
Rattler (Crotalus atrox)r + +
Cobra (Naja naja)g,i + +
Viper (Vipera aspis)h,i + +
Elaph (Elaph quadrivergata); + +

* Not a definitive distinction from oxytocin.

a Sawyer eta!. (1961). b Heller and Pickering (1961).' Follett (1967). d Sawyer (1968).' Acher
eta!. (1972). r Munsick (1966). 8 Pickering (1967). h Acher eta!. (1969b).; Acher eta!. (1969a).

Table 5.2. Distribution of adrenocortical steroid hormones in reptiles

Corticosterone Aldosterone

Crocodilia
Alligator mississippiennsisa + +
Crocodylus nilotocisb + +
Chelonia
Pseudemys spp.' + +
Emys orbicularis' + +
Chrysemys pictad + +
Testudo hermanni' +
Lacertilia
Lacerta viridis' + +
Anolis carolinensil +
Uromastix acanthinurus8 + +
Tiliqua rugosa8 + +
Varanus gouldiih +
Ophidia
Natrix natrix'·; + +
Hydrophysis cyanocinctusi + +
Rhyncocephalia
Sphenodon punctatusk +

aGist and DeRoos (1966). b Balment and Loveridge (1989). ' Macchi and Phillips (1966). d
Sandor et a!. (1964). ' Phillips et a!. (1962a) . r Licht and Bradshaw (1969). s Bradshaw and
Grenot (1976). h Bradshaw and Rice (1981). i Phillips and Chester Jones (1957).; Duggan and
Lofts (1979). k Tyrrell and Cree (1998).

135
kidneys of several reptiles (Capelli et al. 1970}. While renin from mammals and
birds interacts only with plasma angiotensinogen from their own phyletic groups,
that of the reptiles is less fastidious. It can also react, to produce angiotensin,
with the plasma substrate from birds and amphibians (Nolly and Fasciola 1973}.
Angiotensin II from turtles and an alligator is identical to that from cattle, the
domestic fowl and the bullfrog (Fig. 2.6). However, its decapeptide precursor,
angiotensin I is different and has an amino acid substitution at position 9. Rep-
tilian prolactin, when administered to other vertebrates, displays a similar spec-
trum of activities, such as milk let-down in mammals and crop sac secretion in
pigeons. Nevertheless, its structure differs. Prolactin from a sea turtle has a 75%
homology in its amino acid sequence to that of the human hormones (see Bentley
1998}. It is uncertain if prolactin has a role in the osmoregulation of reptiles, but
the possibility has been considered.
Reptiles have a water content equivalent to about 70% of their body weight, an
amount similar to that of birds and mammals, though less than that of the
Amphibia. The concentration of the body fluids conforms to the usual tetrapod
pattern, being about 250 to 300mosmoll-1• Variations in the concentration and
electrolyte content of the body fluids do, however, occur; reptiles in a marine envi-
ronment have a slightly higher plasma concentration than those living on land
(Table 1.2) though they remain hyposmotic to sea-water. Reptiles can tolerate
quite large changes in the concentrations of their body fluids; the sodium con-
centration in the plasma of the lizard, Trachysaurus rugosus, may rise from 150
to nearly 200mEql- 1 during the dry Australian summer (Table 1.2} and compa-
rable increases have also been observed in the lizard, Amphibolurus ornatus,
and the desert tortoise (Dantzler and Schmidt-Nielsen 1966; Bradshaw and
Shoemaker 1967; Bradshaw 1970). Such osmotic behaviour has been called
"ahomeostasis" (Peterson 1996}. Decreased plasma electrolyte levels can also be
readily tolerated; the softshell turtle, Trionyx spinifer, normally has a plasma
sodium concentration of about 150mEql-1, but in healthy hibernating individu-
als this may decrease to 80 mEq 1-1 (Bentley, unpubl observ). Birds and mammals
do not seem to be able to withstand such variations in the concentrations of their
body fluids, but in some reptiles such tolerance may be an important factor in
their ability to survive adverse conditions when the possibility of osmotic regu-
lation is limited.
Reptiles are ectotherms and so, unlike birds and mammals, do not usually
utilize evaporative water loss for thermal cooling. Nevertheless, they do attempt
to maintain their body temperature at levels that are optimal for their activity and
discreetly utilize external heat sources for this purpose. This is performed prin-
cipally by conforming to a certain pattern of behaviour: warming by periodic
basking in the sun and opposing the ventral body surface to warm surfaces, and
cooling by seeking shade and refuges, such as rock crannies and burrows, where
the temperature is more moderate. Modification of the body temperature may be
assisted physiologically by changing the conductivity of the body by means of cir-
culatory adjustments. Some species can change the colour of their skin so as to
alter the rate of absorption of solar radiation (see Schmidt-Nielsen 1964a}. Such
adjustments are probably mediated principally by the nervous system, though in
some reptiles melanocyte-stimulating hormone mediates colour change (Waring

136
1963). Evaporation of water from the respiratory tract and skin increases when
the temperature of the body and the environment rises, but this is physically
obligatory and cannot be considered as part of a regulatory response to facilitate
cooling.
The principal avenues for the exchange of water and solutes between the reptile
and its environment are basically the same as in mammals and birds. The physi-
ological significance and magnitude of the exchanges through the different chan-
nels differ however. The main osmoregulatory organs are the kidneys, as in all
vertebrates, but in certain reptiles the action of these organs may be augmented
by cephalic "salt" glands, and the cloaca-colon and urinary bladder.

1 Water Exchanges

1.1 Skin and Respiratory Tract

In a terrestrial environment reptiles lose water by evaporation from the external

integument, and the lungs and pulmonary passages. This loss increases when
body temperature and environmental temperature increase; thus, the bobtail
goanna, Trachysaurus rugosus, when kept in dry air at 25 °C, loses water by evap-
oration at the rate of 0.7 g (100 gt 1 day- 1 while at 37.5 oc it is 2.9 (100 gt 1day- 1
(Warburg 1965a). This water loss is small relative to that in birds, mammals and
the Amphibia, and makes little contribution to thermal cooling; the temperature
of the goannas when equilibrated to such conditions being only 1 or 2 oc less than
that of the environment.
The increased evaporation of water at high environmental temperatures is due
to the decrease in the saturation deficit for water in the surrounding air, and an
increase in the body temperature of the animal. The metabolic rate of reptiles
increases two to three times for every 10°C rise in body temperature (Benedict
1932), so that there is an increased rate of gas exchange in the lungs that further
facilitates water loss.
Different species of reptiles have been observed to lose water by evaporation
at various rates (Bogert and Cowles 1947). The reasons for such differences were
not initially clear, as they could involve several factors such as: the rate of oxygen
consumption, the ratio of surface area to body weight or the particular proper-
ties of the skin of the different species. This was not further investigated until
Schmidt-Nielsen (1964a) suggested, after examining the fragmentary information
that was then available, that cutaneous evaporation in reptiles may be greater and
more variable than was hitherto considered likely. When cutaneous and pul-
monary water losses were measured separately in a variety of species of reptiles
(at 23 oq, the movement through the integument was indeed found to contribute
from 66 to 87% of the total evaporative loss in a desert lizard, the chuckwalla, to
88% in the brown water snake (Schmidt-Nielsen and Bentley 1966; Schmidt-
Nielsen et al. 1966a; Prange and Schmidt-Nielsen 1969). At higher temperatures,
35 to 40 °C, pulmonary water loss increases relative to that from the skin. However,
the latter still amounts to about 50% of the total. Similar observations have been

137
made on a variety of lizards (Claussen 1967). Some legless burrowing worm-
lizards (family Amphisbaenidae) have even greater rates of evaporative water loss.
They have a cutaneous permeability to water that approaches that of amphibians
(Krakauer et al.1968). The rates of such evaporative water loss appear to be related
to the ecological habitat that is normally occupied by each species of reptile. Thus,
the aquatic brown water snake loses water by evaporation 13 times more rapidly
than the desert -dwelling chuckwalla.
Water loss from the respiratory tract depends on the rate of oxygen consump-
tion and the ability to extract this gas from the inspired air. The metabolic rate
varies considerably in different reptiles, reflecting their activity, size and whether
they happen to be in states of aestivation or hibernation. Such differences are
partly reflected in their rates of water loss. For instance, at 23 oc the desert gopher
tortoise, which has an oxygen consumption of 0.26mlg-1 day-\ loses 0.4mgwater
g- 1 day-1 from the respiratory tract. On the other hand, the forest-dwelling Iguana
iguana has an oxygen consumption of 2.6 ml g-1 day- 1 and loses 3.6 mg water g-1
day-1in this manner (Bentley and Schmidt-Nielsen 1966; Schmidt-Nielsen and
Bentley 1966). However, the relationship between oxygen consumption and water
loss varies in different reptiles. This difference may be due to the proportion of
oxygen extracted from the air in the lungs. There is usually a reduction of oxygen
from the atmospheric levels of 20.9% to 17 to 20%. However, some reptiles only
breathe sporadically (breath holding) and then can extract more oxygen from the
inspired air. The chuckwalla sometimes breathes only two to three times an hour
and then reduces the oxygen level in its lungs to as little as 5% of that present in
the atmosphere (Schmidt-Nielsen et al. 1966a). This behaviour has also been
observed in hibernating reptiles and three species of Australian lizards (genus
Varanus) (Thompson and Withers 1997). In the latter, at 25°C, respiratory water
loss can then decline to about 6o/o of the total water lost by evaporation. Respira-
tory water loss in reptiles can also be reduced in some species by utilizing a coun-
tercurrent heat exchange process in the nasal passages. This mechanism reduces
the temperature, and hence the water vapour content of the expired air (Murrish
and Schmidt-Nielsen 1970a). This strategy, as described earlier, also occurs in
small mammals and birds.
Evaporative water losses in reptiles are probably temporally regulated, in con-
junction with the body temperature, by changes in behaviour. Reptiles may be
diurnal or nocturnal in their habits and avoid extreme temperatures by seeking
the shelter of cool refuges. Warburg (1965a) found goannas, Trachysaurus rugosus,
in burrows 2 to 3m deep. The temperature in these holes never exceeded 28°C,
even though the external air temperature was as high as 40 oc and that of the
surface soil 50 °C.
Many species of reptiles live an aquatic life submerged in fresh water or sea-
water. The air that they breathe is nearly saturated with water vapour, so that little
respiratory loss is expected to occur. However, the osmotic gradients between
their body fluids and the external solution will tend to favour a net water uptake
in fresh water and a loss in sea-water. These exchanges of water are usually quite
small in reptiles. Such gains of water in freshwater turtles, the softshell turtle,
Trionyx spinifer, and the slider turtle, Pseudemys scripta, were found, respectively,
to be 26 and 6mgcm-2 day- 1 (Bentley and Schmidt-Nielsen 1970). The difference

138
appears to be due to the nature of their skin. When these turtles were placed in
sea-water they lost water at the rate of, respectively, 38 and 10mgcm- 2 day- 1 (sea-
water is an unnatural environment for these turtles and it is possible that it
changes the permeability of their skin). Juvenile salt-water crocodiles in sea-water
were found to lose water across their integument at the rate of 2.4mgcm-2 day- 1
(Taplin 1984). However, young caiman, which normally live in fresh water, lost
water at a much greater rate, 14mgcm- 2 day- 1, when in an equivalent salt solution
(Bentley and Schmidt-Nielsen 1965). Measurements of water exchanges, in sea-
water, have been made in freshwater and marine snakes using tritiated water to
measure the influx, from the sea-water and the efflux from the snakes' body fluids
(Dunson 1978). Such fluxes of water were both very low. However, they were
greater in the freshwater species.
There are folkloric tales that some terrestrial reptiles may be able to absorb
water across their integument from dew or damp surfaces. However,
closer scrutiny of such reports in the Australian desert lizard Moloch horridus
indicated that, while water uptake could occur from such sources, it takes place
through the mouth (Bentley and Blumer 1962). The water is absorbed into narrow
open channels on the skin surface and it travels along these to the lips, where it
is collected and swallowed. Small accumulations of water may also occur across
the buccal membranes of aquatic snakes (Dunson 1978) and crocodilians (Taplin
1988).

1.2 Urinary and Faecal Water Loss

Reptiles, like birds and amphibians, possess a cloaca into which the colon, ureters
and reproductive ducts open. It is thus not always easy to separately measure
urinary and faecal losses of water and solutes. However, tortoises and turtles, some
lizards and the tuatara (Sphenodon) have a urinary bladder. This receptacle is
absent in crocodilians, snakes and most lizards. However, in some lizards, the
colon may store substantial amounts of urine and have a bladder-like appearance.
The cloaca, colon and urinary bladder are the sites of water and salt exchanges
that modify the composition of the urine and faeces. As reptiles cannot form
hyperosmotic urine, such processes may make important contributions to their
salt and water economy. The water content of the faeces of reptiles appears to be
usually about 50 to 60g (lOOgt 1 wet weight (Minnich 1970; Nagy 1972). The loss
of water in the urine and faeces in reptiles varies considerably. It has been found
to be as little as 5% of the total water loss each day in the carnivorous side-
blotched lizard Uta hesperis (Claussen 1967) to 60% in the desert iguana Dip-
sosaurus dorsalis (Minnich 1970). Carnivorous reptiles generally lose less water
in the faeces than herbivorous ones, who may excrete large masses of incompletely
utilized plant material. Separate urinary losses have been measured in some rep-
tiles and vary from 15% of the total water loss in the desert snake, Spalerosophis
cliffordii (Dmi'el and Zilber 1971), to 6% in the gecko,Hemodactylus (Roberts and
Schmidt-Nielsen 1966). The relative water loss in the urine can be much higher
in aquatic species, such as the caiman. In small juvenile animals in fresh water it

139
was equivalent to nearly 30% of their body weight each day (Bentley and Schmidt-
Nielsen 1965).

7.2.1 Role of the Kidney

Reptiles, like birds and mammals, have a metanephric kidney. The nephrons
usually begin with a glomerulus and Bowmans capsule, which is followed by a cil-
iated neck segment, proximal tubule, intermediate segment and distal tubule that
opens into a collecting duct system. They lack a loop of Henle and countercur-
rent concentrating mechanism and hence cannot form hyperosmotic urine. A
venous renal portal system is present that supplies the tubules, but not the
glomeruli. Some reptiles, including some snakes and the desert lizard Ctenopho-
rus ornatus have some aglomerular nephrons (O'Shea et al. 1993). This morpho-
logical loss appears to be an adaptation to life in arid environments. The
formation of urine follows the usual vertebrate pattern of plasma filtration across
the glomeruli and subsequent reabsorption of water and solutes during passage
of the filtrate along the renal tubule (Braun and Dantzler 1997). Tubular secretion
of solutes, and in aglomerular nephrons presumably water, also takes place. Such
processes can result in the formation of a dilute, hyposmotic, urine and the con-
servation of essential solutes such as Na+, K+, cl- and HC0 3-. Excesses of such ions,
uric acid and water appear in the urine. When water is not abundant, urine that
approaches isosmoticity with the plasma may be formed. The excretion of uric
acid involves both its glomerular filtration and secretion, which occurs mainly
across the proximal tubule. Uric acid is the principal excretory product of nitro-
gen metabolism in most reptiles, especially snakes and lizards. The crocodiles
can also utilize ammonia for such excretion and tortoises and turtles, urea. As
described in Chapter I, uricotelism can result in a substantial reduction of urinary
water loss that is especially important in predominantly terrestrial and desert-
living species. Uric acid can also form insoluble sodium and potassium salts
which are deposited in the cloaca of reptiles, thus facilitating a more osmotically
economic way for excreting these ions (Minnich 1972).
The glomerular filtration rate in reptiles is usually quite labile, and changes can
contribute to the regulation of water and salt excretion (Braun and Dantzler 1997).
Decreases in the GFR take place in response to dehydration and increases fol-
lowing the ingestion of excess water (Dantzler 1992). The experimental adminis-
tration of sodium chloride usually, though not always, decreases the GFR. Changes
in the GFR in reptiles are mainly due to increases or decreases in the number of
functioning glomeruli (glomerular intermittency). However, small changes in the
filtration rate across individual, single, glomeruli may also occur. Such variations
in glomerular activity are principally due to vascular responses, which appear to
involve the afferent glomerular arteriole.
The neurohypophysis contributes to the regulation of the urine flow in reptiles.
Vasotocin is their antidiuretic hormone. Information about the precise mecha-
nism of its antidiuretic effect is more fragmentary than in birds and amphibians.
In 1933, Burgess et al. showed that the administration of the mammalian neuro-
hypophysial hormones vasopressin and oxytocin had an antidiuretic effect in an

140
alligator (Alligator mississippiensis). However, in contrast to mammals, this
decrease in urine flow was solely due to a reduction in the GFR with no detectable
change in renal tubular water reabsorption. Sawyer and Sawyer in 1952 confirmed
this observation. Extracts of the neurohypophysis of the lizard Tiliqua (Tra-
chysaurus) rugosa were observed to have an antidiuretic effect when injected into
this reptile (Bentley 1959). Subsequently, it became apparent that this action prin-
cipally reflected the presence of vasotocin in the neurohypophysis of reptiles. The
administration of purified vasotocin was also shown to have an antidiuretic effect
in water snakes, Nerodia (Natrix) sipedon (Dantzler 1967). Mesotocin, the other
reptilian neurohypophysial peptide, also has an antidiuretic action, but only when
administered in supraphysiological doses. An antidiuretic effect of vasotocin has
also been demonstrated in the painted turtle Chrysemys scripta (Butler1972;
Dantzler 1982 ). In the water snakes, low doses of vasotocin were observed, by mea-
suring the clearance of water relative to the GFR, to increase the water reabsorp-
tion across the renal tubule. A decrease in the GFR was also observed, but only
when using higher doses of vasotocin. A similar difference in the sensitivity of
the kidney has been observed in the slider turtle following the administration of
extracts of its neurohypophysis (Dantzler and Schmidt-Nielsen 1966). The differ-
ential sensitivity of the glomerular and renal tubular responses is similar to that
described in the domestic fowl (Chap. 4). Whether or not it applies to most rep-
tiles, including the alligator, is unknown. Attempts to demonstrate a direct effect
of vasotocin on isolated renal tubules of reptiles have, so far, been unsuccessful
(Stolte et al. 1977; Beyenbach 1984). However, a vasotocin-sensitive adenylate
cyclase, which mediates water permeability responses in mammals and amphib-
ians, has been identified in the collecting ducts of the lizard Ctenophorus ornatus
(Bradshaw and Bradshaw 1996). Receptors for vasotocin were also identified, but
in the intermediate segment of the renal tubule. A mechanism that could be medi-
ating a permeability response to vasotocin thus appears to be present. The role of
vasotocin receptors in the intermediate segment is unknown.
Neurohypophysial function in the lizard Ctenophorus ornatus can be blocked
by placing electrolytic lesions in the hypothalamo-hypophysial tract (Bradshaw
1976). The GFR was increased. Urine volume, in response to administered saline,
was also increased. The administration of vasotocin decreased the urine volume
and increased renal tubular water reabsorption. The results suggested a physio-
logical role for vasotocin in controlling urine volume in this reptile.
Direct measurements of vasotocin in the blood of the lizard Varanus gouldii
were made, using a radioimmunoassay, by Rice in 1982. Release of the hormone
from the neurohypophysis was related to the osmotic concentration of the
plasma. The concentrations of vasotocin were found to be 3.9pgml- 1 in dehy-
drated lizards as compared to 1.6pgml- 1 in the hydrated ones. The osmotic con-
centrations of the plasma that induced release of vasotocin (osmotic sensitivity)
were similar to those in other vertebrates. The antidiuresis that occurred in
response to dehydration of these lizards was not accompanied by a decrease in
the GFR.It appears to involve only a tubular response (Bradshaw and Rice 1981).
However, following saline loading, the plasma vasotocin levels were increased to
7.1 pgml- 1and a decrease in GFR was then observed. Vasotocin has also been iden-
tified in the plasma of the snake Bothrops jaraca (Silveira et al. 1992), the green

141
turtle Chelonia mydas (Figler et al. 1989) and the lizard Tiliqua rugosa
(Fergusson and Bradshaw 1991).
It is noteworthy that neurohypophysial pep tides exert other actions in reptiles.
They may reduce the blood pressure, as in Trachysaurus rugosus (Woolley 1959)
and Natrix sipedon (Dantzler 1967), but high doses are required, so that these
effects are probably only of pharmacological significance. Vasotocin (in vitro)
contracts the oviduct of the turtle, Pseudemys scripta, when it is in an ovulating
condition (Munsick et al. 1960). LaPointe (1969) has shown that vasotocin also
contracts the oviduct of the viviparous island night lizard, Klauberina riversiana,
in vitro. Oxytocin and mesotocin were very much less effective than vasotocin. It
is possible that this action of vasotocin reflects a physiological role for this peptide
in reptilian oviposition and parturition, just as oxytocin assists the latter process
in mammals.

1.2.2 Role of the Cloaca-Colon Complex

The deposition of solid pellets of uric acid in the cloaca of reptiles suggests that
changes in the composition of the urine are occurring at this site. Differences in
the composition of urine collected directly from the ureters and that expelled
from the cloaca confirm that such changes are occurring. They involve not only
the cloaca, but also the adjoining colon. In some lizards, large accumulations of
urine can be seen in the colon, which then takes on a bladder-like appearance.
Although intestinal caecae are present in some reptiles, they lack the recta caecae,
which contribute to the modification of the urine in birds. The ureteral urine of
reptiles is usually hyposmotic, while that excreted from the cloaca is isosmotic.
This observation suggests that absorption of water is occurring at a postrenal site.
An absorption of salts also takes place. These processes have been studied in
several crocodilians (Bentley and Schmidt-Nielsen 1965; Schmidt-Nielsen and
Skadhauge1967; Kuchel and Franklin 1998), snakes (Junqueira et al. 1966) and
lizards (Braysher and Green1970; Murrish and Schmidt-Nielsen 1970b; Bentley
and Bradshaw 1972; Bradshaw 1975; Skadhauge and Duvdevani 1977; Bradshaw
and Rice 1981). The processes of such absorption have been studied in vivo, in
vitro and using in vivo perfusion techniques. A comprehensive summary of the
available information has been compiled by Don Bradshaw (1997).
The calculated reabsorption of fluid from the cloaca-colon complex of reptiles
varies from 20% in a crocodile (Crocodylus acutus) to 96% in a lizard (Scleloporus
cyanogenys). This absorption appears to be due to an initial osmotic equilibra-
tion with the plasma and a reabsorption of Na+, which, in turn, establishes further
osmotic gradients. Potassium may be either reabsorbed or secreted. In the desert
iguana, the colloidal osmotic pressure of the plasma proteins may also promote
water reabsorption (Murrish and Schmidt-Nielsen 1970b). In the Israeli desert
lizard, Agama stellio, fluid reabsorption from the cloaca-colon complex increases
from 2.4 mlkg-1 h- 1 when they are normally hydrated to 3.3 mlkg- 1 h- 1 during
dehydration (Skadhauge and Duvdevani 1977). In the Australian desert lizard,
Varanus gouldii, reabsorption of fluid from the urine in the cloaca-colon increases
from 22% in hydrated lizards to 40% in dehydrated ones (Bradshaw and Rice

142
1981). However, a hormonal basis for such absorption has not been established
(Bradshaw 1997). A possible role for vasotocin in promoting osmotic water move-
ment has been investigated on several occasions. However, with a single excep-
tion (Braysher and Green 1970), such an action has not been demonstrated. Local
changes, such as involve osmotic gradients, may be determining the reabsorption.

7.2.3 Role of the Urinary Bladder

The urinary bladder of reptiles can be quite voluminous, especially in turtles and
tortoises. It is osmotically permeable to water and so may act as a reservoir for
the storage of water. However, snakes and many lizards that live in deserts do not
have a urinary bladder, so that such an opportunity is not available to all reptiles.
Nevertheless, tortoises utilize the urinary bladder as a water-storage organ, espe-
cially during times of drought and when there are extended periods of time
between access to drinking water (Nagy 1988; J0rgenson 1998). Naturalists and
explorers, including Charles Darwin (1839), have commented on the large
volumes of fluid held in the urinary bladders of species such as the Indian giant
tortoise and the Galapagos tortoise. These quantities of fluid can be equivalent to
as much as 20% of their body weight. Initially, the fluid appears to be quite limpid
and, as commented on by early travellers, can even provide a beverage for thirsty
humans. However, as observed in the tortoise Gopherus agassizii in the Mohave
Desert, the solute concentration rises considerably in times of drought. The con-
tained fluid then approaches isosmoticity with the plasma. It mainly contains
potassium salts obtained from their herbivorous diet and is retained until fresh
drinking water becomes available. In these tortoises, the fluid in the bladder
appears to act as a large "sink" (or cesspool) for the storage of unwanted solutes.
The osmotic permeability of the chelonian urinary bladder has been measured,
in vitro, in the Mediterranean tortoise Tesudo graeca (Bentley 1962b) and the
freshwater turtle Pseudemys scripta (Brodsky and Schilb 1965). Water absorption
was not found to change in the presence of vasotocin. These observations are in
contrast to the effects of this hormone on the urinary bladder in the amphibians
(see Chap. 6). Water absorption has also been measured from the urinary bladder
of the gopher tortoise in vivo. Water introduced into the bladder was found to be
absorbed at the rate of 20 ml h-I in either hydrated or dehydrated tortoises (Dant-
zler and Schmidt-Nielsen 1966). Salt can be reabsorbed from the reptile urinary
bladder (see the next section), which may enhance the osmotic gradient for water
reabsorption. Evaporative water loss is relatively slow in reptiles, so that the
normal rate of its absorption from the urinary bladder may be adequate for their
needs. A hormonally induced response may not be advantageous.
Reptiles that live in hot desert environments where adequate food and water
is available only sporadically may resort to aestivation to reduce water loss and
the consumption of energy. Such a state of dormancy occurs in hot conditions.
(Hibernation, which some reptiles also undergo, occurs in response to cold in
winter.) Aestivation appears to be initiated by a reduction in the food supply and
the drying out of the vegetation, soil and pools of water. It occurs in various rep-
tiles including turtles, lizards, snakes and crocodiles (Gregory 1982). Oxygen con-

143
sumption may decline by as much as 70% (Halley and Loveridge 1997) below
levels that normally occur at a particular body temperature. There is an accom-
panying decrease in evaporative water loss, especially from the respiratory tract
(Seidel 1978). Physiological activities, including kidney function, are drastically
reduced and, depending on the period of dormancy, large increases in the osmotic
concentration of the plasma usually occur. The reptiles sequester themselves in
various places that provide thermally benign environments including rock
crevices, burrows and vegetation. When the pools of water in which they live dry
up, long-necked turtles, Chelodina rugosa, which live in tropical northern Aus-
tralia, dig themselves into the soil (Grigg et al. 1986; Kennett and Christian 1994).
They then await the next rains, which may not occur for two or three seasons.
Under such conditions the turtles lose weight, which includes fat and, mainly,
water. Nevertheless, they can survive. Other reptiles that live in desert conditions
undergo less rigorous periods of aestivation. In the Mohave Desert, following the
drying out of the vegetation in mid-summer, chuckwalla lizards cease eating
(Nagy 1988). They then retire to rock crevices from which they emerge for only
an hour or so every 3 days. The desert tortoises under such conditions spend
longer periods, on average 6 days, in burrows.

2 Salt Exchange
2.1 Skin

The relative impermeability of the integument considerably impedes the move-

ments of salts across the body surface of freshwater and marine reptiles. Precise
values for the permeability to Na+ are difficult to obtain and assess as they are so
low and their measurement is subject to experimental errors. Calculations based
on measurements in whole animals may be overestimated in salt water, due to the
possibility of drinking and uptake across buccal and cloacal membranes and
the eyes. Observations performed on the skin in vitro are also prone to error, due
to the leakage through peripheral regions of skin maintained between clamps that
separate the solutions on each side of the skin (Dunson 1978). When juvenile
caiman are kept in distilled water there is a net loss of Na+ across their skin
amounting to about 1Jlmol cm-2 h- 1 (Bentley and Schmidt-Nielsen 1965). I have
also measured such Na+ loss in softshell turtles, Trionyx spinifer, in distilled water
and found it to be similar to that of the caiman. Loss (unidirectional efflux) of
Na+ across the integument of marine green turtles, Chelonia mydas, has been
measured, using isotopic Na+, in sea-water and fresh water (Kooistra and Evans
1976). In sea-water the efflux amounted to only about 5% of the total sodium loss.
When placed in fresh water, the loss of Na+ decreased from 5.8Jlmol (100gt 1
h-1, in sea-water, to 0.9jlmol {100 gt1 h-1• This difference in permeability could be
due to a direct effect of the bathing solution on the skin, a change in transcuta-
neous electrical potential difference or vascular changes. The permeability, in sea-
water, of the skin of a variety of terrestrial, freshwater and marine snakes has been

144
investigated (using isotopic Na+) both in vivo and in vitro (Dunson 1978). The
skin of the marine snakes was virtually impermeable to Na+, but a small influx of
this ion, from sea-water, could be detected in the freshwater species. The skin of
the estuarine (salt-water) crocodile was also found to be almost impermeable to
Na+ (Taplin 1985). Movements of Na+ across the skin of aquatic reptiles appear to
make little contribution to their salt balance. However, other integumental mem-
branes are more permeable to Na+ (and water) especially those of the mouth, eye
and cloaca. Such routes may be the sites of significant exchanges of salts and, pos-
sibly, in crocodiles, even active ion accumulation (Taplin 1988).

2.2 Kidney

The urine of reptiles may contain excess salts, especially sodium and potassium
chlorides, which are usually obtained in the diet. In circumstances when there is
an excretion of excess water by the kidney, the salt excretion in the urine will be
reduced by its reabsorption across the renal tubule. The formation of urine by the
kidneys in reptiles, as described earlier, usually involves substantial changes in
the GFR, and hence the rate of delivery of water and solutes to the renal tubules.
The proportion, or "fraction", of Na+ that is reabsorbed varies considerably, from
more than 98% to as little as 50% (Bradshaw 1997). About 60 to 70% is thought
to occur in the proximal tubule and the remainder in the distal tubule and col-
lecting ducts (Braun and Dantzler 1997). Potassium is reabsorbed in the proxi-
mal tubule and, when necessary, can be secreted by the distal tubule. Considerable
variations have been observed in the osmotic and electrolyte concentrations of
the urine in reptiles. The ratio of the urine/plasma osmotic concentrations can
vary from 0.1 to 1. The lowest salt concentrations are usually seen in freshwater
species, which have a surfeit of water. When the estuarine diamondback terrapin,
Malaclemys centrata, is maintained in fresh water, the urine concentration is
about 60mosmoll-1 and its Na+ concentration is less than 1 mEql-' (Bentley et al.
1967a). I have found that the urine of softshell turtles maintained under such con-
ditions has a similar concentration of sodium. However, Roberts and Schmidt-
Nielsen (1966) found that in three species of lizards (gecko, horned toad and
Galapagos lizard) the concentration of Na+ in the ureteral urine was always about
100 mEq 1-', even when the animals had been hydrated. Solute reabsorption from
the renal tubule varied from about 50% in the Galapagos lizard to 85% in the
geckos. The experimental administration of various amounts (loads) of sodium
chloride to reptiles often results in a decrease of the GFR compared to that of
hydrated animals (see Bradshaw 1997). (However, this effect can be variable and
it is not, for instance, seen in some snakes.) The administration of sodium chlo-
ride loads to the bobtail lizard Tiliqua (Trachysaurus) rugosus and the gopher tor-
toise results in anuria, which appears to reflect a glomerular shutdown (Bentley
1959; Dantzler and Schmidt-Nielsen 1966). In the bobtail, even small loads of
sodium chloride are poorly excreted, only about 20% appearing in the urine over
a period of 24h. Renal responses to the administration of potassium chloride are

145
somewhat more rapid, apparently reflecting a renal tubular secretion of the K+
(Shoemaker et al. 1966). However, the reptile kidney appears to generally have a
poor ability to excrete excess salt, especially when water is restricted. This defi-
ciency can be compensated for in two ways. Some reptiles have a remarkable
ability to tolerate high concentrations of Na+ in their body fluids. This ability was
observed in the laboratory and, in summer, in free-ranging bobtail lizards
(Tiliqua rugosus) in Australian coastal sand dunes (Bentley 1959). Bradshaw and
Shoemaker {1967) found that plasma sodium chloride concentrations of Amphi-
bolurus lizards rise as high as 300 mmoll- 1 during periods of drought in desert
areas in Australia. Following a summer rainstorm, the lizards were observed to
dart about and rapidly drink the water as it fell. After 10 h the plasma electrolyte
concentrations had returned to normal. The desert tortoise also utilizes such
occasions to drink and excrete solutes that have accumulated in its urinary
bladder (Nagy 1988). Other reptiles, as will be described later in this chapter, prin-
cipally utilize cephalic salt glands for the excretion of excess sodium and potas-
sium chlorides.
In mammals the adrenal cortex, and its secreted steroidal hormones, has an
established role in promoting the reabsorption of Na+ and the secretion of K+ by
the distal renal tubule-collecting duct system. These effects are principally
mediated by aldosterone. Such hormonal effects also occur at extrarenal sites,
including the colon. Experimental investigations of the possible roles of the
adrenocortical tissue on such processes in reptiles have yielded inconclusive
results. In mammals, adrenalectomy results in a rise in the concentration of
K+ in the plasma and a decline in that of Na+. Adrenalectomy is a difficult
procedure in reptiles due to the dispersal of the tissue and its association with
large blood vessels. Cauterization of the adrenocortical tissue in the bobtail
lizard resulted in an increase in the concentration of K+ in the plasma but no
change in Na+ (Bentley 1959). A similar response was observed following adrena-
lectomy in another Australian lizard, Varanus gouldii (Rice et al. 1982). The
failure to detect an expected decline in the Na+ concentration in the plasma
could be reflecting the tardy metabolism of these cold-blooded animals. Elizondo
and LeBrie ( 1969) induced adrenocortical insufficiency in a water snake, Nerodia
(Natrix) cyclopion, by occluding the blood supply to the tissue. Sodium, as well
as K+, concentrations in the plasma decreased. The painted turtle, Chrysemys
picta, responds to adrenalectomy in a more mammal-like manner. The K+ con-
centration in the plasma rises and Na+ declines (Butler and Knox 1970). Study of
the renal function of the "adrenalectomized" water snakes suggested that there
was a decrease in the fractional reabsorption of Na+ across the proximal renal
tubule.
The administration of aldosterone to the intact water snakes during a water
diuresis had no demonstrable effect on renal sodium excretion. However, when
they were first given a load of sodium chloride, this hormone increased the frac-
tional reabsorption of Na+ by the renal tubule (LeBrie and Elizondo 1969). With
the benefit of hindsight, we now know that the endogenous levels of aldosterone
are high in hydrated reptiles and are decreased by sodium chloride loading
(Bradshaw and Grenot 1976; Bradshaw and Rice 1981). Thus, the effects of admin-
istered aldosterone would be expected to increase following the administration

146
of the salt load. Administered aldosterone has also been shown to decrease Na+
and increase K+ concentrations in the urine of the desert iguana (Templeton et
al. 1972a) and three species offreshwater turtles (Brewer and Ensor 1980).
Aldosterone was first measured in the plasma of reptiles in 1976 by Bradshaw
and Grenot. It was identified in two lizards; Uromastix acanthinurus from Algeria
and Tiliqua rugosa from Australia. The concentrations were similar to those
observed in mammals, and in Uromastix were inversely related to the plasma Na+
levels. Similar observations have since been made in the lizard Varanus gouldii
and the tortoise Testudo hermanni (Bradshaw and Rice 1981; Uva et al. 1982).
However, the concentrations of aldosterone in the plasma were lower in the tor-
toises. The observations of the effects of exogenous aldosterone and its release in
response to changes in the Na+ levels in the plasma are consistent with a physio-
logical role of this hormone on kidney function in reptiles. Corticosterone is also
present in the plasma of reptiles, but its release, in contrast to that of aldosterone,
is increased in lizards by the administration of sodium chloride (Bradshaw et al.
1972; Bradshaw and Rice 1981). In alligators, this corticosteroid is released when
they are placed in dilute sea-water (Lauren 1985). Such release of corticosterone
possibly constitutes a stress response.

2.3 Cloaca and Urinary Bladder

The cloacal-colon complex and the urinary bladder, as described earlier, can be
sites of substantial fluid absorption. In some reptiles the renal tubular reabsorp-
tion of Na+ is quite low and further conservation of this ion occurs at these
extrarenal sites. Various observations have been made in vitro demonstrating the
presence of an active Na+transport mechanism in the cloaca-colon of the caiman,
the Mediterranean tortoise, snakes and several lizards (Bentley 1962a; Bentley and
Schmidt-Nielsen 1965; Junqueira et al. 1966; Bentley and Bradshaw 1972; Diaz and
Lorenzo 1992). The process of Na+ reabsorption has also been studied using in
vivo perfusion techniques in lizards (Skadhauge and Duvdevani 1977; Bradshaw
and Rice 1981). The rate of such Na+ transport is reduced in Varanus gouldii
following the administration of sodium chloride (Bradshaw and Rice 1981).
However, the change could not be related to the concentrations of vasotocin or
aldosterone in the plasma. The Na+-dependent electrical short-circuit current (in
vitro) across the colon of the Mediterranean tortoise and Amphibolurus lizards
was unaffected by vasotocin (Bentley 1962a; Bentley and Bradshaw 1972).
However, aldosterone has been shown to increase such Na+ transport, in vitro,
across the colon of the lizard Gallotia gallati (Diaz and Lorenzo 1992). As
described earlier, aldosterone has ubiquitous effects in increasing Na+ reabsorp-
tion, including the colons of mammals and birds. Its effect on the lizard colon is
reminiscent of these actions.
The urinary bladders of turtles and tortoises are the site of active Na+ reab-
sorption from the urine (Brodsky and Schilb 1960; Bentley 1962a). This process
can be increased, in vitro, by aldosterone (Bentley 1962a; LeFevre 1973). In con-
trast to amphibian urinary bladders, vasotocin has no effect on such ion trans-

147
port in the Mediterranean tortoise or the bobtail lizard (Bentley 1962a; Bentley
and Bradshaw 1972).
The urinary bladder and cloaca of turtles may also be involved in the accu-
mulation of sodium from the external environment. Pseudemys cripta exchange
sodium with bathing fluids at the rate of 0.04 to 10 j.l.mol (100 gt 1 h- 1 (Dunson
1967). When the cloaca is blocked, this rate of exchange is reduced by 70%, indi-
cating that the processes of sodium transfer in the cloaca and urinary bladder
may be involved. Turtles are known to irrigate their cloacal regions with the fluid
that bathes them, so that an active transport of sodium in such regions could
mediate a net accumulation of this ion by turtles. In the softshell turtle, Dunson
and Weymouth (1965) consider that active sodium transport across the pharynx
may be responsible for such solute collection.
The cloaca-colon complex and, when present, the urinary bladder of reptiles,
appear to have the capacity to reabsorb, and hence conserve, substantial amounts
of Na+ from the urine. Information regarding possible hormonal control of this
process is meagre. However, the fragmentary information that is available sug-
gests that, as in mammals and birds, aldosterone could be contributing to such
regulation.

2.4 Cephalic Salt Glands

Like their avian descendants, many reptiles also utilize salt glands for the secre-
tion of concentrated, hyperosmotic, solutions of sodium chloride. Unlike birds,
some reptiles can also secrete solutions of potassium chloride. The salt glands of
reptiles are more morphologically diverse than the nasal salt glands in birds.
There may also be differences in the manner that they regulate the composition
of these fluids. Schmidt-Nielsen and Hinge in 1958 first described the function-
ing of reptile salt glands in the loggerhead turtles and the diamondback terrapin.
These salt glands are not nasal glands but modified supraorbital ("tear") glands.
However, like birds, the marine iguana, which lives on the shores and reefs of the
Galapagos Islands, utilizes a nasal gland for this purpose. Many other lizards
utilize such lateral nasal glands for salt secretion. The salt glands that are present
in sea snakes are submaxillary glands that lie under the tongue. Somewhat unex-
pectedly, the estuarine (salt-water) crocodile also has been found to possess salt
glands that lie in the tongue (Taplin and Grigg 1981). These lingual salt glands
have been found in other crocodiles, but not alligators. Salt glands are alsoappar-
ently not present in terrestrial snakes and have been described only in a single
terrestrial chelonian, Testudo carbonaria (Peaker 1978). Salt glands appear to have
evolved several times in the reptiles. In marine and intertidal species, they secrete
solutions that are hyperosmotic to sea-water and have a Na/K concentration ratio
over 30: 1. In terrestrial herbivorous lizards, they form equally concentrated solu-
tions but they principally contain potassium chloride and have KINa ratios as
high as 80/1 (Table 5.3). Such K+ secretion appears to be dictated by the ion
content of their plant diet.

148
Table 5.3. Sodium and potassium secretion by the salt glands of reptiles

Concentration Ratio Rate of Habitat

mEql- 1 Na/K J.tEqkg- 1 h- 1
Na+ K+ secretion
Na• K+

Crocodilia
Crocodylus porosus• 509 11 46 49 Estuarine
Chelonia
Malaclemys centratab 784 70 Estuarine
Caretta carettab 878 31 28 Marine
Chelonia mydas' 685 21 33
Testudo carbonariad 0.1-6 233-260 0.01 Terrestrial
Lacertilia
Sauromalus obesus' 44 430 0.1 3 27 Desert
Dipsosaurus dorsali/·8 494 1387 0.35 22 31 Desert
Uromastyx aegyptu/ 639 1398 0.46 Desert
Amblyrhynchus cristatush 1434 235 6 2550 510 Marine
Tiliqua rugosa' 167 433 0.39*
Ophidia
Laticauda semifasciatak 686 57 12 730 33 Marine
Pelamis platurus1 620 28 22 2180 92 Marine

• Taplin and Grigg (1981). b Schmidt-Nielsen and Fiinge (1958).' Holmes and McBean (1964).
d Peaker (1978). ' Templeton (1964). r Schmidt-Nielsen et al. (1963). 8 Templeton (1966).
h Dunson (1969). 1 Bradshaw et al. (1984b). k Dunson and Taub (1967). 1 Dunson (1968).
* Potassium loading.

The process of the initiation of secretion by reptilian salt glands has not been
studied in as much detail as that in birds. It may even vary in different species.
The administration of an analogue of acetylcholine, methacholine, usually
stimulates secretion (Schmidt-Nielsen and Hinge 1958; Templeton 1964; Taylor
et al. 1995). This effect is consistent with control by the parasympathetic nervous
system, as occurs in birds. The administration of hyperosmotic solutions of
sodium chloride initiates secretion. However, in some reptiles, hyperosmotic solu-
tions of sucrose are not an effective stimulus. Hyperosmotic solutions of potas-
sium chloride promote salt gland secretion in herbivorous lizards, but sodium
chloride is also, though somewhat less, effective (Templeton 1964; Grenot 1967;
Braysher 1971; Shoemaker et al. 1972b; Shuttleworth et al. 1987}. The submaxil-
lary glands of sea snakes and the lingual glands of crocodiles respond to the
administration of hyperosmotic solutions of sodium chloride (Dunson and
Dunson 1974; Taylor et al.1995}. The initiation of the neural processes that appar-
ently control secretion thus appear to reside in receptors responsive to hyperos-
motic concentrations of sodium chloride or potassium chloride. Their precise
sites have not been identified in reptiles but, as described earlier in birds, they
may be associated with the hypothalamus. The presence of a cholinergic nerve
supply to the supraorbital gland of the diamondback terrapin has been ques-

149
tioned (Belfry and Cowan 1995). The nerve supply to these glands was found to
contain vasoactive intestinal peptide {VIP), but not acetylcholine. Such nerves in
birds usually contain both substances. The nerves supplying the lingual salt
glands of the estuarine crocodile also contain both acetylcholine and VIP
(Franklin et al. 1996). The injection of VIP into these crocodiles evokes a
massive increase in salt gland secretion. Methacholine has been observed to
decrease secretion by the supraorbital salt gland of the green sea turtle (Reina and
Cooper 2000). Administered adrenaline usually decreases salt gland secretion in
reptiles, as also observed in birds. This response appears to reflect a decreased
blood flow to the glands. There are, possibly, differences in the precise mecha-
nisms that are utilized by various reptiles and birds to initiate secretion from their
salt glands.
There has been considerable interest in the possible role of adrenocorticos-
teroids in regulating secretion from salt glands in reptiles. Holmes and McBean
in 1964 found that "chemical" adrenalectomy, with injected amphenone, reduced
salt gland secretion in green sea turtles. This deficiency could be overcome by
the administration of corticosterone. The adrenalectomy also decreased the con-
centration of Na+ in the secretion relative to that of K+. In contrast to this obser-
vation, surgical adrenalectomy in the desert iguana (a potassium secretor)
resulted in a large increase in secretion from their nasal salt glands and a decrease
in the K/Na concentration ratio (Templeton et al.1968, 1972b). These effects could
be reversed by the administration of aldosterone. In the normal lizards, injected
aldosterone reduced Na+ excretion by the salt gland and increased the K/Na
concentration ratio. This effect of aldosterone on the secretion of the salt glands
of the desert iguana was confirmed by Shoemaker and his colleagues {1972b).
They also found that corticosterone and cortisol were effective, but that they
were less potent. These corticosteroids may be mimicking the action of
aldosterone. The administration of aldosterone to the North African desert lizard
Uromastyx acanthinurus, a potassium secretor, also decreased Na+ excretion
by their salt glands (Bradshaw et al. 1984a). The administration of K+ to these
lizards increased, while Na+ decreased, the concentration of aldosterone in the
plasma. The rates of K+ secretion from the salt glands showed a positive
correlation and Na+ excretion a negative correlation with increases in plasma
aldosterone. Repeated administration of sodium or potassium chlorides results
in appropriate adjustments of the relative amounts of these ions excreted by
the salt glands of Uromastix. These changes may be mediated by aldosterone.
Bradshaw ( 1997) proposed that the aldosterone may contribute to the process of
secretion by influencing both its composition and rate. This action could be a
primary one on the metabolism of Na+ and K+by the salt glands. It is reminiscent
of the action of aldosterone on the mammalian kidney.
The bobtail lizard Tiliqua (Trachysaurus) rugosa can also adjust the composi-
tion of its salt gland secretion following the administration of solutions of potas-
sium and sodium chlorides (Braysher 1971). The administration of sodium
chloride to this lizard resulted in a modest decline in the concentration of aldos-
terone in the plasma. However, in contrast to Uromastix, corticosterone levels
increased (Bradshaw and Grenot 1976; Bradshaw et al. 1984). Binding sites, pos-
sibly receptors, for aldosterone and corticosterone were identified in extracts of

150
the nasal salt glands of bobtail lizards. They had a higher binding affinity for cor-
ticosterone than for aldosterone. It is possible that corticosterone may be stimu-
lating salt gland secretion in these lizards (Bradshaw 1997). Such an effect would
be consistent with the earlier observation of Holmes and McBean ( 1964) in green
turtles. A return to this study of the possible roles of adrenocorticosteroids in
turtles would be welcome. Currently, there appear to be no observations on the
possible effects of adrenocorticosteroids on the salt glands in crocodiles or sea
snakes.

3 Accumulation of Water and Salts

Water and salts are acquired by reptiles from their food and by some species as
a result of drinking. Only small accumulations of water and salts can take place
across the integument of aquatic species. Carnivorous reptiles generally appear
to obtain adequate water from their diets. Some such reptiles, including the Nile
crocodile (Balment and Loveridge 1989), the estuarine crocodile (Taplin 1984),
sea snakes (Dunson 1969) and the estuarine diamondback terrapin (Bentley et al.
1967a) have been observed to drink fresh water when it is available. Terrestrial
herbivores, such as tortoises and lizards, generally consume succulent plants,
which usually contain a surfeit of water. However, some conditions, such as life in
hot arid environments, evaporative water loss and an excessive intake of salt in
the food, may result in drinking behaviour. Drinking in such reptiles may occur
periodically following rainstorms, such as observed in gopher tortoises in the
Mohave Desert (Nagy 1988) and Amphibolurus lizards in arid regions of Australia
(Bradshaw and Shoemaker 1967). Schmidt-Nielsen (1964a) described the copious
drinking of a desert tortoise that consumed water equivalent to 40% of its body
weight in a single such session. Charles Darwin (1839) commented on the promi-
nent drinking habits of the tortoises on the Galapagos Islands. Desert tortoises
have even been observed to construct water catchment basins to trap rainwater
(Medica et al. 1980).
Amphibians do not drink, so the reptiles appear to be the first tetrapod
vertebrates to have developed this custom. As described earlier, mammals and
birds may be induced to drink following the administration of angiotensin II
(Kobayashi et al. 1979; Kobayashi and Takei 1997). Such a drinking response to
injected angiotensin II has also been observed in representatives of the main
phyletic groups of reptiles. Most species exhibited such drinking responses.
However, the Mediterranean tortoise failed to respond. The tropical lizard Anolis
carolinensis was relatively unresponsive. The tortoise is adapted to life in dry
regions and Anolis, which is insectivorous, has little need for drinking water in
nature. The relative lack of an angiotensin II-induced drinking response in such
reptiles is reminiscent of such insensitivity in some desert mammals and birds
(Chaps. 3 and 4). Hibernating reptiles were also found to be unresponsive to
angiotensin II.
It is uncertain whether marine reptiles voluntarily drink sea-water. In the estu-
arine crocodile, an ability to discriminate between salt water and fresh water, and

151
to avoid drinking the former, may be vital for its survival during its marine expe-
ditions (Taplin 1988). Similar conclusions have been drawn with respect to the
abilities of related species of water snakes to survive in salt water (Pettus 1958).
The freshwater snakes could not survive in salt water, and their demise was attrib-
uted to drinking. The salt water species did not drink.

4 Reproduction and Osmoregulation

The need for water may influence reproduction in reptiles. The amniotic mem-
brane, which encloses the fluids in which the embryo develops, facilitates repro-
duction on dry land. It first appeared in the reptiles. This important innovation
is associated with the enclosing of the egg in a shell. Such cleidoic eggs are per-
meable to gases and water. They also contain the allantoic membrane into which
crystals of insoluble uric acid are deposited. Some reptile eggs contain sufficient
water for normal embryonic development but others, especially among squamate
reptiles, take up additional water. Water may even be lost from the eggs as a result
of evaporation or osmosis. Reptiles thus usually deposit their eggs in damp situ-
ations where such losses may be limited. Additional water may even be gained
during development in such "nests". Reptiles are usually oviparous, but some,
such as sea snakes and many lizards, retain their eggs, which develop in the
oviduct (ovoviviparous). Some species are even viviparous.
The eggs of reptiles are sometimes guarded by the parents, but the young are
usually left to fend for themselves. Their survival depends on many factors, and
in hot dry conditions can be influenced by the availability of succulent food and
moisture. Such juvenile reptiles, with their relatively high surface area, can be par-
ticularly susceptible to evaporative water loss. Thus, reptiles, like other verte-
brates, may reproduce when the availability of water and food favours the survival
of the eggs and young. The timing of reproductive cycles in reptiles appears to be
more related to the environmental temperatures than the photoperiodic cues that
are predominant in mammals and birds (see Bentley 1998). Endogenous repro-
ductive rhythms may also be important. In desert reptiles, reproduction may
cease in periods of drought, as seen in the chuckwalla lizards in the Mohave
Desert (Nagy 1988). In contrast, desert tortoises, which live under similar condi-
tions, lay their eggs even during drought conditions. Some reptiles, such as Scle-
roporus lizards, practice egg retention until the substrate conditions are damp
enough to fruitfully deposit their eggs (Andrews and Rose 1994; Mathies and
Andrews 1996).A release of vasotocin could be playing a role in such oviposition.
The access of water to the eggs of turtles and tortoise can result in the develop-
ment of larger hatchlings that are better able to survive the vicissitudes of over-
land migrations to water (Packard 1999). Such adaptations in the patterns of
reproduction in reptiles clearly involve changes in the release and actions of hor-
mones. They may influence the onset of breeding behaviour, ovulation and the
development of the eggs, oviposition and parturition. Possible adaptations in
desert species include differences in the permeability of the eggs to water, the size

152
of the clutch and the times taken for the eggs to hatch. Viviparity has evolved
many times in vertebrates, including the reptiles. In cold-blooded animals it is
usually considered to provide a more controlled temperature for embryonic
development. However, in species living is dry arid conditions, it could also
provide a more equitable osmotic situation for the development and survival of
the young.

153
Chapter 6

The Amphibia

The Amphibia bridge the phyletic gap between the fishes and terrestrial tetrapod
vertebrates. This transition has involved considerable osmoregulatory, as well as
respiratory, change so that water and salt metabolism may be expected to be par-
ticularly varied and interesting. For both these reasons, and the relatively free
liaison between physiologists and amphibians, the group has received consider-
able scientific attention.
The Amphibia arose from a crossopterygian fish in Devonian times. This tran-
sition is generally thought to have occurred in sea-water. There is only one sur-
viving crossopterygian fish, the coelacanth, Latimeria chalumnae, which was not
found until 1938. This coelacanth is a marine species, several of which have been
caught off the southeast coast of Africa. The contemporary Amphibia are repre-
sented by three orders: the Apoda, the Urodela and the Anura. The Apoda, or
caecilians, are small, shy worm-like animals, of which there are about 17 genera,
living exclusively in tropical equatorial areas of America, Africa and Asia. Unfor-
tunately, very little is known about their physiology and there is little informa-
tion about their osmoregulation. The Urodela, or the Caudata, contain the newts
and salamanders of which there are 43 genera, mostly confined to temperate
regions in the Northern Hemisphere and completely absent from Australia.
The Anura are the most numerous of the three orders, containing more than
200 genera which are widely distributed around the world. "Nothing - neither
climates, nor deserts, nor mountains nor even narrow gaps of salt water - has
prevented the spread of dominant frogs over the world in the course of time"
(Darlington 1957). Anurans are present on all the major land masses (except
Antarctica), where they occupy habitats ranging from freshwater ponds and
streams, to tropical forests and arid deserts. A few species even venture into the
cold polar regions north of the arctic circle. Many are primarily aquatic, but they
are usually more comfortable in fresh than brackish water. At least one species,
Rana cancrivora, the crab-eating frog, lives in sea-water among mangroves along
coastal areas of Southeast Asia. Darlington (1957) concludes that frogs must have
crossed narrow gaps of salt water, but notes that they usually have a low tolerance
to such solutions, and this presumably accounts, as commented upon by Darwin
(1839), for their absence from most oceanic islands. Most amphibians readily lose
water through their permeable skin, so that desert regions may also be expected
to restrict their movements. Nevertheless, while such areas may slow their migra-
tions, they certainly do not stop them.
The amphibians exhibit a number of well-defined physiological differences
from their piscine ancestors and reptilian descendants. Such divergences may
have a considerable influence on the osmoregulation of the respective groups so

155
Table 6.1. Some physiological characters of Amphibia (compared with those of reptiles and
bony fishes) that influence their osmoregulation

Reptilia Amphibia Osteichthyes

Poikilothermic + + +
Branchial respiration (gills) -or+ +
Egg amniotic +
Kidney:
1. Hyperosmotic urine
2. Antidiuretic to neurohypophysial + -or+ - or diuresis
peptides
Urinary bladder derived from cloaca + +
Nitrogen excretion:
_a
Uric acid +
Urea + + +
Ammonia + + +
Drinks water + +
Skin: restricted permeability + +
Extrarenal salt excretion + +
Extrarenal salt conservation + +
Neurohypophysis: neural lobe persent + +
Secretes:
1. Vasotocin + + +
2. Mesotocin + + _b

3. Isotocin +
Adrenocortical tissue secretes:
1. Corticosterone + + +
2. Aldosterone + +
3. Cortisol some(?) +
a In a few xerophilic anurans.
b Present in lungfish.

that I have attempted to summarize some of them (Table 6.1). Perhaps the major
factor that affects amphibian osmoregulation is the adoption, by most of the adult
forms, of atmospheric, instead of aquatic, respiration. The Amphibia are assisted
in this process by gaseous exchanges across their skins (the plethodont salaman-
ders have no lungs and depend solely on their skin for this purpose). As a result,
the skin is also more permeable to water. It has been suggested that the
crossopterygian ancestors of the Amphibia underwent a reduction of their cuta-
neous scales in order to facilitate aeriform respiration (Szarski 1962}.A relatively
impermeable skin was not phyletically restored until the emergence of the rep-
tiles. The other major factor influencing the osmotic life of most amphibians is
the necessity to lay their eggs in water and for the larvae to undergo an aquatic
period of development before they metamorphose into a form which can live
on land. Reptiles have adopted an amniotic and cleidoic egg, which is normally
laid on land, and so have achieved a considerable further measure of osmotic
independence. There are many other differences in the osmoregulatory pattern

156
of fishes, amphibians and reptiles (Table 6.1) that may further hinder or facilitate
their osmotic homeostasis. These will be discussed in subsequent sections.
Water makes up about 80% of the total body weight of most amphibians (see
for instance, Schmid 1965) and this is a higher proportion than the 70% seen in
most other tetrapods. Nevertheless, this may vary; two Australian tree frogs
(family Hylidae), Hyla moorei and H. caerulea, have water contents equivalent,
respectively, to 71 and 79% of their body weights (Main and Bentley 1964). The
osmotic concentrations of the body fluids of amphibians are also usually less than
those of other tetrapods, about 250mosmoll- 1; there is also less sodium present
in the plasma, about llSmEql- 1 • This may also vary a great deal depending on
the particular species, its habitat and osmotic condition (Table 1.2). The North
American spadefoot toad, Scaphiopus couchi, can survive in deserts during
extended periods of drought. McClanahan ( 1967) has shown that when this toad
aestivates in burrows during such dry periods, the concentrations of solutes in its
body fluids rise considerable, from 305 mosmoll- 1 to as high as 630 mosmoll- 1•
These frogs emerge after rain when they hydrate and restore the solutes to more
normal levels. The crab-eating frog, Rana cancrivora, also increases the concen-
trations of its body fluids to very high levels when living in sea-water (Gordon et
al. 1961). Both of these anurans tolerate sodium concentrations up to about 250
mEq 1- 1 in their plasma, while large quantities of urea are also accumulated and
may reach a level of 500 mM. Considerable decreases in plasma solute levels are
also tolerated. Amphibians, even more so than reptiles, thus exhibit a consider-
able ability to tolerate different solute levels in their body fluids.
Tolerance to changes in the osmotic concentrations of the body fluids may vary
in different species and account for their distinctive abilities to withstand differ-
ing degrees of dehydration. In 1943, Thorson and Svihla compared the abilities of
a number of North American frogs and toads to survive desiccation. Their results
indicated that amphibians normally living in more aquatic habitats withstand loss
of their body fluids poorly, compared to those which live in drier areas. Thus, the
aquatic frog, Rana grylio, dies after losing water, by evaporation, equivalent to
about 30% of its body weight, while the spadefoot toad, Scaphiopus hammondi,
can survive a loss of 50% in its body weight. A similar relationship between the
habitat and survival of desiccation has been shown by Schmid {1965) in North
American anurans, and we have also observed this to be so in some Australian
tree frogs (Main and Bentley 1964). Warburg {1967) found that some frogs from
dry regions in central Australia withstand dehydration better than those from
wetter habitats, but he has emphasized the importance of the speed of water loss
in determining the animals' survival. Frogs seem to be able to live longer when
the rate of dehydration is slow than when it is fast, and although I have made no
precise measurements of this, I would agree that this is probably an important
factor. Differences in ability to withstand dehydration are not invariably seen
among different groups of anurans. The Australian genera Neobatrachus and
Heleioporus each have four or five species that have adopted habitats ranging from
wet forests to dry deserts, and they all survive a water loss equivalent to 40 to 45%
of their body weight (Bentley et al. 1958). These Australian frogs (family Lepto-
dactylidae) thus all tolerate water losses as great as those of the best-adapted

157
North American species or of Australian Hylidae. The Australian deserts are far
older than those in North America, and the leptodactylids are an ancient anuran
family that probably gave rise to the now more widely distributed Bufonidae. The
Australian leptodactylids may thus have evolved into a basically xerophilous
group which in the course of long periods of time has adapted more uniformly
to dry conditions. As we shall see, these leptodactylids also have a remarkable
ability to rehydrate rapidly and can store large volumes of water in their urinary
bladders.
Most urodeles live in temperate areas, but some species inhabit more arid
regions such as the deserts of the southwest USA. Some, such as the desert sala-
mander, Batrachoseps aridis, inhabit areas where permanent water seeps exist
(Shoemaker 1988). Adult tiger salamanders, Ambystoma tigrinum, in New Mexico
occupy dry habitats that are similar to those of anurans (Delson and Whitford
1973). Five species of salamanders from temperate areas in North Carolina died
after losing water that was equivalent to 18 to 30% of their body weights (Spight
1968). However, tiger salamanders can survive after losing water equal to 45% of
their body weight (Alvarado 1972). During dry periods, these urodeles burrow
into the damp soil where they apparently aestivate for periods up to 9 months
(Delson and Whitford 1973). Under such conditions they accumulate salt and urea
in their body fluids, which reaches a concentration of 550 mosmoll- 1• The Urodela
appear to have shared a common ancestry with the Anura. An ability to withstand
large increases in the concentrations of their body fluids may have developed
early in amphibian evolution. Caecilians (Apoda) are an order of the Amphibia
which in evolutionary time predated the Anura and Urodela (Stiffler et al. 1990;
Jared et al.1999). Like other amphibians, they have a permeable skin and are prone
to evaporation. Some live an aquatic life or, more usually, they are fossorial and
burrow into damp soil and vegetation. Their ability to withstand desiccating con-
ditions is unknown.
The remarkable ability of many amphibians to withstand water loss and con-
siderable increases in the concentrations of their body fluids is associated with
several aspects of their physiology. They appear to be better able to withstand
such conditions when the rates of their dehydration are slower. They reduce this
process by seeking refuges, such as burrows, rock crevices and damp soil and
vegetation. Urea, instead of being excreted, is retained, and is a substantial com-
ponent of the increased concentrations of their body fluids. The haematocrit
increases during dehydration and the peripheral circulation declines. However,
the water content of the deep visceral organs is maintained (Hillman 1978; Malvin
et al. 1992; Churchill and Storey 1994). Amphibians can also store water in capa-
cious urinary bladders (see later).
Amphibians may live in three contrasting types of osmotic environment: fresh
water, dry land or, very occasionally, in salt water. Larval amphibians, certain
urodeles, such as the mudpuppy and the congo eel, anurans like the South African
clawed toad and the caecilian Typhlonectes compressicauda (Stiffler et al. 1990),
are almost entirely aquatic. Many species habitually live near ponds and streams
into which they make periodic excursions, and they are thus truly amphibious.
The fresh water where such species live, or visit, is hyposmotic to their body fluids
so that there is a continual accumulation of water occurring across their skin. This

158
may be equivalent to 30 to 40% of their body weight in a day and is excreted by
the kidneys as a dilute (hyposmotic) urine. This urine contains only small, but
nevertheless significant, amounts of solutes, and the loss of some of these, espe-
cially sodium and chloride, may be physiologically significant. In addition, as
shown by the classical studies of Krogh (see Krogh 1939), amphibian skin is per-
meable to sodium and chloride, so that on simple physico-chemical grounds one
would expect further losses to occur across the integument. While in certain
unphysiological circumstances, like bathing in distilled water, such losses can be
demonstrated, they are usually prevented by an active transport, by the skin, of
sodium (and sometimes chloride) from the bathing medium.
Darwin (1839) noted that frogs have a poor tolerance to salt solutions and
only two species have been discovered for which this is not true. When leopard
frogs, Ran a pipiens, are placed in sea-water they die in 30 to 60 min. Bentley and
Schmidt-Nielsen (1971) found that under these conditions they lose water
through the skin, but the main reason for their demise is not water loss, but
a massive accumulation of salt that takes place through their skin and as a result
of drinking. Even when these frogs are placed in saline solutions similar in
concentration to their body fluids (0.7% sodium chloride), they often do not
survive for longer than 24 h. In more dilute solutions they live for longer periods,
gaining weight due to the accumulation of salt and water (Adolph 1933). Never-
theless, some anurans do habitually enter brackish water and at least one, the
crab-eating frog, Rana cancrivora, lives in sea-water (Gordon et al. 1961). The
European green toad, Bufo viridis, has been found in ponds where the salt con-
centration, while less than that of sea-water, is a substantial2% (Gislen and Kauri
1959). There are other reports of amphibians being found in brackish water, but
it is often difficult to judge how typical such an event is in the life of the animal.
The sight or sound of an approaching naturalist can conceivably strike sufficient
terror into a frog to prompt it, unwittingly, to leap into a pool of salt water. Gordon
(1962) collected Bufo viridis in different areas of Europe ranging from Naples to
Belgrade and found that these toads, in common with Rumanian ones previously
studied by Stoicovici and Pora (1951), could live for extended periods of time in
solutions with a sodium chloride content of 2% or sometimes even more. It is,
indeed, considered to be euryhaline (Katz 1973; Hoffman and Katz 1997). The
most basically important osmotic adjustment Bufo viridis and Rana cancrivora
make towards their life in saline solutions is to initiate and maintain the concen-
trations of their body fluids at levels that are always, sometimes only slightly,
hyperosmotic to the bathing fluids. This elevation in the osmotic pressure of the
body's fluids results from an elevation of the sodium levels and, particularly in
the instance of Ran a cancrivora, an accumulation of urea (Table 1.2). The tadpoles
of Rana cancrivora, however, like all amphibian larvae, cannot form urea, but
utilize a completely different mechanism for their life in sea-water. They main-
tain their body fluids, like those in bony fishes, at a concentration which is hypos-
motic to sea-water, possibly excreting excess salt through their gills (Gordon and
Tucker 1965).
When amphibians utilize their inherent ability to live on dry land, they are
potentially subject to an osmotic stress that is initiated in a manner different from
that in sea-water, that of evaporation from the integument. Evaporation from the

159
skin is characteristically rapid in the Amphibia as compared to other tetrapods.
Nevertheless, amphibians, especially anurans, have successfully occupied arid
areas in which high environmental temperatures and a low content of water
vapour in the air considerably facilitate evaporation. Such species utilize a
number of mechanisms that somewhat mitigate these conditions. Like all verte-
brates living in such places, they have adopted patterns of behaviour that reduce
the times of exposure to the extremes of the environment; they seek refuge in
cracks in rocks, and burrow, often deeply, into the soil. In addition, a variety of
physiological processes affect the osmoregulation of such amphibians.
The amphibians, like other tetrapods, are aided in their osmoregulation by
the action of some hormones, the most important being those secreted by the
neurohypophysis and the adrenocortical tissues.
The neurohypophysial hormones in amphibians are of both phyletic and his-
toric interest. They represent the debut of these hormones in tetrapod vertebrates.
They have assumed novel roles concerned with the adaptation to terrestrial life.
The neurohypophysis of amphibians and other tetrapods is, compared to that
of the fishes, enlarged, and forms the neural lobe (Wingstrand 1966). This mor-
phological change is associated with a greater storage of its peptide hormones.
However, some aquatic amphibians, such as the mudpuppy Necturus maculosus,
retain a more fish-like neurohypophysis. Historically, the study of the amphibian
neurohypophysial hormones has played a pivotal role in the emergence of our
knowledge of the nature and actions of such hormones in non-mammals. In 1941,
Hans Heller observed anomalies in the pharmacological activities of extracts of
the neural lobes of English frogs (Rana temporaria). Such extracts, like those
obtained from mammals, when injected into frogs produce a gain in weight due
to the retention of water (Brunn 1921). This action is known as the Brunn effect
or water balance response. (It is a composite response and reflects the ability of
the hormone to produce an antidiuresis and increased osmotic water transfer
across the skin and urinary bladder. The magnitude of the response varies in dif-
ferent species.) Heller standardized his amphibian neurohypophysial extracts by
measuring their ability to produce an antidiuresis in rats. Equivalent doses of such
standardized preparations from mammals and frogs were then administered to
frogs. The neurohypophysial extract from the amphibian was found to be far more
active than the mammalian one. Heller suggested that it contained a novel con-
stituent, which he called the amphibian water balance principle. Nearly 20 years
later, this "principle" was found to be the peptide hormone 8-arginine-vasotocin
(Pickering and Heller 1959; Sawyer et al. 1959; Acher et al. 1960). It is generally
referred to as vasotocin or AVT (Fig. 2.5). Subsequently vasotocin was identified
in representatives of the main phyletic groups of non-mammalian vertebrates. A
second peptide separated chomatographically from such extracts of the amphib-
ian neurohypophysis, based on its pharmacological behaviour, initially, appeared
to be oxytocin. However, in 1964, Follett and Heller (1964a) found that it behaved
differently to oxytocin in some pharmacological bioassay systems. It behaved
more like 8-isoleucine-oxytocin, which had earlier been prepared experimentally
by chemical synthesis. The novel structure of the natural hormone was confirmed
and it was called mesotocin (Acher et al. 1964). This hormone was subsequently

160
 .,
Ill
0
~
u
..s

Moles Peptide I kg

Fig. 6.1. Water balance effects of vasotocin (L',.), oxytocin (e) and mesotocin (0) in toads
(Bufo marinus). Note: Log-dose scale. (Bentley 1969a)

found to have a wide phyletic distribution, including birds, reptiles and even lung-
fish and kangaroos. It remains possible that oxytocin may also be present in the
neurohypophysis of some amphibians (Munsick 1966). Vasotocin, mesotocin and
oxytocin can all promote water retention in various amphibians, but vasotocin is
by far the most potent of these peptides. In the cane toad Bufo marin us it is 200
times more active than mesotocin (Fig. 6.1).
More recently, other vasotocin-like and oxytocin-like peptides have been iden-
tified in the amphibian neurohypophysis. Seritocin (5-serine, 8-isoleucine-
oxytocin) has been identified in an African toad, Bufo regularis (Chauvet et al.
1995). Two natural structural analogues of vasotocin have been found in the
amphibian neurohypophysis. They exhibit a similar ability to stimulate water and
Na+ transfer (in vitro) across amphibian skin and urinary bladder. However, in
contrast to vasotocin, they have little antidiuretic activity in rats or frogs ( Acher
et al. 1997). They have been called hydrins, and are formed from the precursor of
vasotocin, provasotocin, as a result of differences in the cleavages of amino acids
at the C-terminus. Hydrin 1 is a dodecapeptide that is present in the neurohy-
pophysis of the aquatic toad Xenopus laevis. It is vasotocinyl-Gly-Lys-Arg. Hydrin
2 is a decapeptide that is present in the families Ranidae and Bufonidae. It is vaso-
tocinyl-Gly. Such C-terminal-extended natural analogues of vasotocin have, so far,
not been identified in other vertebrates. (They are reminiscent of attempts by

161
pharmacologists to produce drug preparations of "impeded" neurohypophysial
peptides that have prolonged activities.) The precise physiological roles of the
hydrins are unknown. They could be providing more selective effects, such as an
increase in water absorption across the skin and urinary bladder without infl~­
encing renal function.
The principal adrenocorticosteroids that are synthesized by amphibians are
aldosterone and corticosterone (Carstensen et al. 1961; Johnston et al. 1967;
Vinson et al. 1979; Henderson and Kime 1987). They have been identified in vitro
in incubation media containing adrenocortical tissue and also in the plasma of
the bullfrog Rana catesbeiana and the toad Bufo marinus. They have also been
identified in the plasma of Xenopus laevis (Chan and Edwards 1970; Jolivet-Jaudet
and LeLoup-Hatey 1984) and several urodeles including the congo eel and larval
tiger salamanders (Stiffler et al. 1986). Cortisol has been identified in some
amphibians, but it does not appear to be predominant (Chester Jones et al. 1959;
Krug et al. 1983). It is interesting that lungfish possess aldosterone and corticos-
terone, like the amphibians, but also cortisol, which is predominant in bony fish.
Aldosterone, as in other tetrapods, has the greatest mineralocorticoid activity.
When assayed, in vitro, for its ability to increase Na+ transport across frog skin it
is 100 times more potent than corticosterone (Yorio and Bentley 1978). Cortisol
was about ten times less active than corticosterone. The synthesis and release of
corticosteroids in anuran amphibians can be increased by ACTH and the renin-
angiotensin system (DuPont et al.1976).ACTH has also been observed to increase
aldosterone secretion in urodeles (DeRuyter and Stiffler 1986). The increased syn-
thesis of aldosterone and corticosterone that occurs in response to ACTH can be
inhibited by atrial natriuretic peptide (Lihrmann et al. 1988).
Amphibians have an active renin-angiotensin system but lack a discrete juxta-
glomerular apparatus. However, renin-secreting cells have been identified in their
renal vasculature (Kobayashi and Takei 1997). Amphibian renin is relatively non-
specific as, apart from amphibians, it can also interact with angiotensinogen from
birds and reptiles (Nally and Fasciola 1973). Bullfrog angiotensin I differs from
that of other vertebrates by the substitution of asparagine at position 9 (Fig. 2.6).
However, the active peptide angiotensin II has the same structure as that of cattle,
reptiles and birds, though it differs from that of fish.
Natriuretic peptides (ANP-like, BNP-like and CNP-like) have been identified in
the heart and brain of bullfrogs (Sakata et al. 1988; Yoshihara et al. 1990; Fukuzawa
et al. 1996).
Prolactin is present in the amphibian pituitary gland and in some species it
may influence their osmoregulation. It has a structure that is analogous to that in
other tetrapods and it has a similar spectrum of biological activities (for instance
stimulation of milk letdown in mammals and crop sac secretion in pigeons). In
the bullfrog the homology of its amino acid sequence to that in humans is 65%
(see Bentley 1998). It appears to be more closely related to that in lungfishes than
any other vertebrates. Two distinct forms of prolactin have been identified in the
toad Xenopus laevis (Yamashita et al. 1993).

162
1 Water Exchange

1.1 Skin

Skin plays a major role in the osmoregulation of the Amphibia, due not only to
its high permeability to water and salts, but also to the fact that such permeation
may vary in different species and be subject at times to physiological regulation.

1.1.1 In Water

Amphibians do not drink, except in certain non-physiological situations as

when they are placed in hyperosmotic salt solutions. Instead, water moves
across the skin, a process that occurs down a gradient of osmotic concentration.
When the solutions on either side of the skin are osmotically equal, little water
is transferred. If the external solution is that of an impermeant solute like sucrose,
virtually no water transfer occurs. If a permeant solute, such as sodium, is pre-
sent, small movements of water, consistent with isosmotic solute transfer,
may occur in order to maintain osmotic equality. Such transfer of water is
normally minor. The movement of water across the skin of frogs and toads is
directly proportional to the osmotic gradient between the two sides of the skin
(Sawyer 1951). The movement of water is thus considered to be a passive process,
not requiring the direct intervention of any metabolic energy. Normally, it is from
the outside solution into the animal, but if amphibians inadvertently enter hyper-
osmotic solutions they lose water; in Rana pipiens placed in sea-water, water
passes out across their skin at the rate of 55Jllcm- 2 h- 1 (P.J. Bentley, unpubl
observ).
The rate of water transfer across the skin differs by species. Schmid ( 1965) has
measured the rates of osmotic water transfer across the skins (in vitro) of six dif-
ferent species of North American frogs and toads. He found that the skins of
aquatic species like the mink frog, Rana septentrionalis, had a lower permeabil-
ity to water (6fll cm-2 h- 1) than those from more terrestrial species like the Dakota
toad, Bufo hemiophrys (20Jllcm-2 h- 1). Frogs from habitats judged to be interme-
diate in their "dryness" showed correspondingly different permeabilities. The skin
from anurans with low permeability to water was found to have a higher lipid
content than those with a higher permeability (Schmid and Barden 1965).
This osmotic water transfer across the skin of terrestrial toads, Bufo marinus
and B. bufo, is, respectively, 28 and 19Jllcm- 2 h-r, while in the aquatic Xenopus
laevis it is 7Jllcm-2 h- 1 (Maetz 1963; Bentley 1969a). The skin of adult bullfrogs
is about four times more permeable to water than that of their tadpoles (Bentley
and Greenwald 1970). Similar differences have been observed among the urode-
les. The skin of adult tiger salamanders is about twice as permeable to water
as that of their aquatic larvae (Bentley and Baldwin 1980). The skins of aquatic
mudpuppies and congo eels are even less permeable to water. Osmotic water
uptake in an aquatic caecilian, Typhlonectes compressicauda, was found to be
about one-third of that in a terrestrial species, Ichthyophis kohtaoensis (Stiffler et
al. 1990).

163
 When dehydrated amphibians return to water they regain water by absorbing
it across their skin. They can also take up water in this way from damp surfaces
such as soil. The ability of the Amphibia to gain water from damp earth presum-
ably depends on the moisture content of the soil and the various forces (osmotic,
hygroscopic and capillary) that tend to hold water there. The water content of the
soil may be quite variable, depending on such things as when rain last fell, the
presence of surface vegetation and the proximity of groundwater. Spight (1967a)
found that the six species of salamanders studied by him could absorb water from
a soil sample that contained about 10% water. When the moisture content was
lower, 3 to 4%, the salamanders slowly lost water, showing that the forces con-
trolling water retention by the soil may also have a dehydrating action on the
animals. However, it was apparent that these salamanders, which were mostly
native to North Carolina, should be able to absorb water from the soil in the agri-
cultural areas of this region at any time of the year. Such an ability to gain water
from soil is an important factor in the ability of the fossorial spadefoot toad,
Scaphiopus couchi, to survive in dry desert conditions (Shoemaker 1988). In 1952,
W. T. Stille observed the nocturnal ramblings of three species of frogs (family
Ranidae) and a toad, Bufo woodhousii fowleri, on a beach in southern Lake Michi-
gan. The toads appeared to search for areas of suitably damp sand to which they
apposed the "skin of the groin area" for the replenishment of their body water.
The frogs, on the other hand, entered the lake to rehydrate.
When amphibians are dehydrated, they usually absorb water through their skin
more rapidly than when they are normally hydrated. There is considerable vari-
ability in the magnitude of this pro~ess; it may be slow, as seen in aquatic species
like Xenopus laevis, or fast, as in the terrestrial toad, Bufo carens. Such observa-
tions on these two species led Ewer (1952b) to suggest that such a response may
be better developed in species that are normally terrestrial in their habits as com-
pared to more aquatic species. Parallel with these observations it was found that
when neurohypophysial peptides were injected, Bufo retained large amounts of
water, while Xenopus completely failed to respond. These differences are remi-
niscent of the observations of Steggerda (1937), who found that while terrestrial
species of the Amphibia accumulated large quantities of water after being injected
with preparations of mammalian neurohypophysial peptides, aquatic ones
retained little. An ability to rehydrate rapidly could be important to some amphib-
ians, particularly to those living in areas where water is available only sporadi-
cally and quickly disappears either by evaporation or soaking into the soil. It is
also possible that entry into open pools of water may increase the risk of attack.
Thus, a facilitated rate of absorption would reduce exposure to predators. The
rates of rehydration in a large number of North American and Australian am-
phibians have been measured, and compared in relation to the availability of
water in the habitats where they normally live. It is evident that there is consid-
erable divergence in the rates of rehydration, but just how uniformly this may be
related to the habitat, thus representing a physiological adaptation, is not clear.
Rehydration in a large variety of North American frogs and toads from
the families Ranidae, Bufonidae, Hylidae and Pelobatidae has been measured
(Thorson 1955; Claussen 1969), but no relationship between the rate of water
accumulation and the "dryness" of the habitat was found. A number or Australian

164
frogs, especially those from the family Leptodactylidae, have also been examined
for evidence of such a correlation. We (Bentley et al. 1958) confined our studies
to species within the genera Heleioporus (five species) and Neobatrachus (four
species). The habitats of species within these two genera range from areas in
which rain falls regularly, on an average of 120 days a year, to desert, or semidesert
regions, where the annual rainfall may be spread over only a few days. Frogs of
the genus Heleioporus all rehydrated at similar rates (about 50j.tlcm- 2 h- 1) after
being dehydrated to 75% of their normal weight. However, species of Neobatra-
chus showed considerable differences in their abilities to absorb water after such
dehydration; N. pelobatoides, which lives in areas where rain usually falls on
60-120 days a year, gain water at the rate of 33j.tlcm-2 h- 1, while N. wilsmorei,
which lives in dry areas towards the interior of the continent, regains water at the
rate of nearly 100 j.tl cm- 2 h- 1• It is notable that such differences in ability to rehy-
drate were paralleled by the rates at which these frogs accumulated water after
being injected with a neurohypophysial peptide, oxytocin. The failure of Heleio-
porus to show any evidence of a correlation between water uptake and the aridity
of the habitat could reflect the ability of this group to avoid the excesses of the
climate by deep burrowing in friable sandy soils, thus making rehydration ability
somewhat redundant. Warburg ( 1965b) has also found that frogs that live in the
arid and semiarid central regions of Australia rehydrate more rapidly than those
species that live in more temperate areas. Few urodeles have been examined
for their ability to rehydrate following dehydration, but Spight (1967b) measured
this in four species of salamanders. He found only relatively small increases in the
rates of water absorption by dehydrated animals, the maximum rate of water
uptake being observed in Ambystoma opacum, and this was only 10j.tlcm- 2 h- 1•
Urodeles also accumulate water only slowly after being injected with neuro-
hypophysial peptides (see Heller and Bentley 1965).
Whether or not the rate of water absorption through the skin following dehy-
dration can be related to the habitat of the species is not clear. Such a correlation
certainly does not exist among all species. Nevertheless, considerable diversity
does exist, and this reflects differences in the permeability of the skin that range
from about 4j.tlcm- 2 h- 1 in dehydrated Xenopus to as much as 420 j.tlcm-2 h- 1 in the
ventral pelvic skin in Bufo punctatus (McClanahan and Baldwin 1969). In addi-
tion, the permeability of the skin may be augmented during dehydration, in such
a manner as to suggest the presence of a regulatory mechanism. In view of these
observations, I feel that it is reasonable to suppose that such differences arose and
persisted in response to ecological stresses on the Amphibia during their evolu-
tionary history, even though they may not today be precisely related to the life of
all contemporary species.
The rate at which amphibians may gain water is directly related to the rate that
water passes across their skin. This may depend on several factors. As shown by
Schmid's (1965) studies, the permeability to the skin of anurans may differ even
in the absence of dehydration, and this will, of course, contribute to the differ-
ences observed in the rates of rehydration. The permeability of the skin to water
may, as we have seen, be augmented in dehydrated animals, and this could result
from several effects. Due to the increased concentration of the body fluids, the
osmotic gradient across the skin increases during dehydration, and water would

165
be expected to move along this gradient more rapidly. Such effects must be rela-
tively small, but could contribute to minor increases in water absorption, as Spight
observed among urodeles. The increased osmotic pressure of the body fluids
probably also exerts a direct action on the skin and increases its permeability to
water, such as has been observed in the urinary bladders of toads (Bentley 1964).
In 1936, Novelli found that neurohypophysial extracts could increase the per-
meability of the skin of anurans to water; this action has since been shown to be
widespread within this group, especially terrestrial species. The response is absent
in Xenopus, which is aquatic, and poor in Rana cancrivora, which is euryhaline
(Maetz 1963; Bentley 1969a; Dicker and Elliott 1969, 1970). The effects of such
peptides on the osmotic permeability of the skin of many urodele amphibians,
including the tiger salamander, fire salamander (Salamandra maculosus) and
alpine newt (Triturus alpestris), are often small or undetectable (Bentley and
Heller 1964, 1965; Bentley and Baldwin 1980). However, cutaneous responses to
neurohypophysial pep tides have been described in the semiarboreal newt Aneides
lugubris, the terrestrial, but not the aquatic, phase of Triturus vitatus and the
California newt Taricha torosa (Hillman 1974; Brown and Brown 1980). Mam-
malian neurohypophysial hormones, like vasopressin, can exert such an action on
anuran skin, but the amphibian peptide, vasotocin, is far more active. Bourguet
and Maetz (1961) found that it increased the permeability of the skin of Rana
esculenta even when present at the concentration of only 10-10M. Vasotocin is
released into the blood of dehydrated frogs and toads in which it is present at a
concentration of 10-9 to 10-10M, which should be adequate to mediate increases in
the permeability of the skin of dehydrated anurans. Other hormones possibly
could also be involved; thus, adrenaline has been shown to increase (in vivo) the
osmotic permeability of the skin of toads, Bufo melanostictus (Elliott 1968) and
frogs in vitro {Jard et al. 1968). This response appears to be a ~-adrenergic one
(Yokota and Hillman 1984). In Bufo cognatus isoproterenol, which is a selective
~-adrenergic analogue of adrenaline, increased cutaneous water uptake. Propra-
nolol, a ~-adrenergic antagonist drug, blocked 60% of the expected cutaneous
water uptake following dehydration. Such an adrenergic effect on water move-
ment across the skin may reflect a sympathetic nerve response and could be facil-
itating the action of vasotocin.
The entire body surface of amphibians is not always uniformly permeable to
water, or Na+, nor do all areas of the skin respond equally to neurohypophysial
hormones. In 1969 McClanahan and Baldwin observed that dehydrated toads,
Bufo punctatus, could absorb water across a pelvic area of their skin (the pelvic
patch) at the rate of 420f.llcm-2 h-1• Water absorption across the pectoral region
of the integument of these toads was too small to measure. The ventral pelvic
patch of skin appears to be used for the absorption of water from damp surfaces.
In hindsight, it is consistent with the observations of Stille (1952) on the posture
of rehydrating toads living on the coastline of Lake Michigan. Comparisons, in
vitro, of the permeability, to water and Na+, of skin from different regions of the
integument have been made in several species of amphibians (Bentley and Main
1972; Yorio and Bentley 1977). The permeability to water, and response to vaso-
tocin, were greatest in the pelvic region of the toad Bufo marinus and several
species of tree frogs (family Hylidae). However, the integument was uniformly

166
permeable in Xenopus, which is aquatic, and Neobatrachus, which is fossorial. The
skin of such pelvic patches is more densely vascularized than that in other cuta-
neous areas (Roth 1973; Christensen 1974a). The response to vasotocin, in vitro,
is reduced when the perfusion of these blood vessels is decreased (Christensen
1974b). This effect appears to reflect localized lowering of the osmotic concen-
tration gradient and the buildup of unstirred layers of fluid in the tissue (Parsons
and Schwartz 1991). When the skin is dry and dehydrated there is a reduction in
the circulation in pelvic skin, but on contact with water, perfusion is restored
(Malvin et al. 1992). The mechanism for this effect is unknown, but it could
be due to a decrease in the blood viscosity and changes in neural or hormonal
adrenergic activity.

7.1.2 In Air

Amphibians exposed to air can lose considerable amounts of water by evapora-

tion. The rate of water loss may be 50 to 100 times as rapid as in lizards of similar
size (Clausen 1969). Evaporation from most amphibians appears to occur at a rate
that is similar to that from a free-water surface (Rey 1937; Bentley and Yorio 1979).
As demonstrated by Adolph in 1933, it is not changed in frogs by the presence
of the skin. However, amphibians can avoid and limit such water loss by utilizing
several different strategies. The most common involves their behaviour, noctur-
nal feeding and adopting postures that reduce their exposed surface area. They
often seek cool humid refuges in vegetation, rock crevices and damp soil. Some
amphibians, including many Australian frogs, actively burrow into the soil on
the onset of desiccating conditions. A number of anurans have developed "water-
proofing" mechanisms, which generally involve their exposed dorsal surfaces
(Toledo and Jared 1993). Such waterproof frogs include the genus Chiromantes
(family Rhacophoridae) from Africa, Phyllomedusa (Hylidae) from South
America and Litoria (Hylidae) from Australia. Some amphibians have deposits of
relatively impermeable lipids in their skin or "wipe" lipoidal solutions, secreted
by skin glands, over their integument. African reed frogs (family Hyperoliidae)
(see Chap. 1) accumulate reflective guanine plates in their cutaneous iridophores.
The activities of skin glands, which secrete mucus and lipids, in amphibians
are controlled by sympathetic adrenergic neural, and possibly hormonal, mech-
anisms. In the Indian tree frog, Polypedates maculatus, which indulges in wiping
behaviour, the secretion from skin glands can be stimulated by the injection of
adrenaline and blocked by the administration of the J3-adrenergic antagonist drug
propranolol (Lillywhite et al. 1997).
Many amphibians, especially those living in regions where rainfall is periodic
and unpredictable, aestivate during times of drought. This process involves
a reduction in their oxygen consumption to levels that may be only 20 to 30%
of their standard metabolic rate (Withers 1993). Such aestivation may occur
in secluded situations, such as burrows, or exposed areas, as seen in African
reed frogs. The osmotic concentrations of their body fluids may gradually
rise under such conditions due to water loss and the progressive accumulation
of urea. Lee and Mercer in 1967 described cocoons composed of layers of shed

167
skin, the stratum corneum, which envelops several species of Australian lepto-
dactylid frogs during their aestivation in burrows. Such cocoons can reduce
evaporative water loss by as much as 97% (Withers 1998a). Layers of the stratum
corneum are progressively accumulated at the same frequency as the moulting
cycle (Withers 1995). Evaporative water loss decreases progressively as the
number of layers increases. Such cocoons have also been observed in frogs from
Africa and North and South America. They are also formed by some urodeles,
including the congo eel (Etheridge 1990}. Moulting in amphibians is a rhythmi-
cal process that normally occurs every few days and is influenced by endocrine
activity arising from the pituitary gland (Budtz 1977}. Following the separation
of the stratum corneum and the formation of the "slough" shedding occurs.
In toads, this shedding can be promoted by the administration of ACTH,
corticosterone and aldosterone. The slough is usually eaten. The accumulation
of layers of the stratum corneum in aestivating amphibians appears to involve
an interruption of normal endocrine activity, but the details of this process
are unknown.

1.2 The Kidney

The kidney of adult amphibians, like that of fishes, is a mesonephros. In the early
stages of larval development, such as in tadpoles, it is a pronephros. The nephrons
usually consist of a glomerulus and Bowmans capsule, a ciliated neck segment,
proximal tubule, intermediate segment and distal tubule. The latter is connected
to the collecting ducts by a connecting segment. There is no loop of Henle. Arte-
rial blood vessels supply the glomeruli and there is a venous, peritubular, renal
portal system. This morphological arrangement of the nephron and its blood
supply is similar to that in the metanephric kidney of reptiles. The amphibians
also lack a capacity to form hyperosmotic urine. The glomeruli are usually quite
large. However, two species of Australian desert frogs have been found to only
have "rudimentary or degenerate" glomeruli (Dawson 1951). Nevertheless, their
kidneys are not completely aglomerular.
Amphibians provided the first experimental preparations for direct observa-
tions, by A. N. Richards, of the processes of the formation of the glomerular
filtrate and renal tubular absorption in vertebrates (see Smith 1951}. The rela-
tively large size and accessibility of the nephron allowed sampling of its fluids
with glass micropipettes. These studies were made using North American leopard
frogs and mudpuppies.
Amphibians in fresh water excrete the water absorbed through their skin as
a dilute urine. An anuran like the European frog, Rana esculenta, which weighs
100g, forms about 60ml of urine during a single day in fresh water (Jard and
Morel1963 ). Urodeles, in the same situation, secrete similar amounts of urine each
day; the mudpuppy (200g) forms about 50ml, while the alpine newt (lOg) pro-
duces 16ml, 160% of the body weight' (Bentley and Heller 1964}. It can be seen
that the daily volume of urine that an amphibian in fresh water may secrete is
considerable, especially in small animals that have a relatively large surface area

168
 in relation to their body weight. When living in sea-water, Rana cancrivora forms
far less urine; this frog, weighing 50 g, forms only about 2 ml of urine each day
(Schmidt-Nielsen and Lee 1962). When amphibians are exposed to a drying
atmosphere, urine formation is too small to measure, and in leopard frogs
amounts to an anuria (Adolph 1933).
The relationship of the processes of glomerular filtration and tubular water
reabsorption to the eventual urine volume has been examined in a number of
amphibians. Both of these mechanisms play a prominent role in the regulation of
the urine volume. The Rana esculenta, referred to above, have a GFR of 125 ml per
day, corresponding to the 60 ml of urine per day, so that about 50% of the filtered
water is reabsorbed under these conditions. In other circumstances tubular water
reabsorption may be greater. The urine volume in Rana esculenta is almost
directly related to the GFR, and in some individual frogs that form urine at twice
the average rate, the GFR is also doubled (Jard 1966). Crab-eating frogs (50 g) in
sea-water filter 30 ml of water per day across their glomeruli but produce only
2 ml of urine, so that more than 90% of the filtrate is reabsorbed. The cessation
of urine secretion that is observed in dehydrated frogs probably results from the
almost complete failure to form a glomerular filtrate. Fewer such observations are
available in urodeles and they are rare in caecilians (Pruett et al. 1991). However,
both glomerular filtration and tubular reabsorption of water and solutes appear
to contribute to the regulation of urine flow in the Amphibia.
Amphibians, in common with reptiles and fishes, cannot secrete urine that
is osmotically more concentrated than their body fluids, so that the ability to
prevent water loss in this way is limited. The urine can attain isosmoticity with
the plasma, as seen, for instance, in aestivating spadefoot toads (McClanahan
1967). In fresh water the urine is markedly hyposmotic, less than 30mosmoll- 1
(see for instance Gordon 1962; Jard and Morel 1963). In sea-water the urine of
crab-eating frogs is intermediate in concentration, being slightly hyposmotic to
the body fluids, 600 mosmoll- 1 compared to 830 mosmoll- 1 in the plasma (Gordon
et al. 1961 ).
Neurohypophysial pep tides when injected have been shown to reduce the urine
volume in many species of anurans and urodeles (Morel and Jard 1968). The
Brunn effect, as described earlier, partly reflects this renal response. The anti-
diuretic effect of the administration of mammalian neurohypophysial extracts
(pituitrin, containing both vasopressin and oxytocin) was initially observed to be
entirely due to a decrease in the GFR (Burgess et al.1933). No effect on water reab-
sorption by the renal tubule was observed. However, in 1952 Sawyer and Sawyer
showed that when such hormone preparations were injected into the toad
Bufo marinus the observed antidiuresis reflected both a decline in GFR and an
increased reabsorption of water from the renal tubule. When it became available
for experimental use, vasotocin was also shown to have such a dual effect during
antidiuresis, not only in the toads but also in bullfrogs and European frogs
(Sawyer 1957; Uranga and Sawyer 1960; Jard and Morel1963). Vasotocin was also
shown to have an antidiuretic effect in several urodele amphibians (Bentley and
Heller 1964; Warburg 1971). However, the contributions of the GFR and renal
tubular water reabsorption to this effect were not investigated. In the California
newt, Taricha torosa, such an antidiuresis was accompanied by an 84% reduction

169
in the GFR (Brown and Brown 1980). The magnitude of the antidiuretic response
to administered neurohypophysial hormone preparations varies considerably in
different species of amphibians. It appears to be smaller in aquatic species, such
as mudpuppies and Xenopus laevis. It is absent or poorly developed in larval
forms of urodeles and anurans (Alvarado and Johnson 1965,1966; Bentley and
Greenwald 1970; Warburg and Goldenberg 1978).
Mesotocin has a diuretic effect when injected into frogs (Jard 1966; Pang and
Sawyer 1978) and several species of urodeles (Stiffler et al.1984). This unexpected
effect appears to reflect a vasodilatatory action on the afferent glomerular arte-
riole, which results in an increased GFR (Pang et al. 1982). Mesotocin has also
been observed to antagonize the antidiuretic effect of vasotocin in frogs (Morel
and Jard 1963). A possible role for mesotocin as a diuretic hormone is still open
to speculation.
Although there are sporadic reports of antidiuretic effects of vasotocin in fish
(see Chap. 7), such a physiological role is generally considered to be unlikely. The
Amphibia appear to be the first vertebrates to have utilized vasotocin as an anti-
diuretic hormone. However, vasotocin is present in all the phyletic groups of ver-
tebrates and has usually been found to be able to elicit vascular responses that
result in an increase in blood pressure. It has been suggested that amphibians first
utilized this vascular response of vasotocin to elicit an antidiuretic effect (Pang
et al. 1982, 1983 ). The ability of vasotocin to increase the permeability of epithe-
lial membranes, such as the renal tubule, to water was a subsequent evolutionary
event. Administered vasotocin can have a diuretic action in lungfish that is
thought to be due to a general vasoconstriction and an increased blood pressure
(called a type-I response). In the mudpuppy there is also a rise in blood pressure
and a small antidiuresis due to a decreased GFR. This type-II effect is thought
to be due to an increase in the vasoconstrictor responsiveness of the afferent
glomerular arteriole. The vasoconstrictor effects of vasotocin are mediated by V1
type receptors. In other amphibians the antidiuretic response to vasotocin
involves both a decline in GFR and an increased permeability of the distal renal
tubule to water (type-III response). The latter is a phyletically novel response to
vasotocin (and vasopressin) that is mediated by Vrtype receptors. In mammals,
it provides the principal mechanism for the antidiuretic action of vasopressin
(type-IV response).
Neurohypophysectomized amphibians still exhibit an antidiuresis in response
to dehydration, despite the absence of vasotocin (Bakker and Bradshaw 1977). The
amphibian kidney has a sympathetic-adrenergic innervation and access to circu-
lating catecholamine hormones. This system may provide an alternate mecha-
nism for the control of urine volume. In 1924, Richards and Schmidt showed
that adrenaline could influence the renal circulation of frogs. Administered
noradrenaline has an antidiuretic effect in bullfrogs (Gallardo et al. 1980; Pang et
al. 1982). The a-adrenergic antagonist drug phenoxybenzamine can inhibit this
response. It can also promote a diuresis in dehydrated frogs. The antidiuretic
response to noradrenaline, like that of vasotocin, is due to a decreased GFR and
an increased reabsorption of water across the renal tubule. Exposure of the skin
of toads, Bufo arenarum, to salt solutions results in a rapid antidiuresis (Petriella
et al. 1989). This effect can be inhibited by blockade of sympathetic nerve activ-

170
ity. Water excretion by the amphibian kidney appears not only to utilize vasotocin
for the control of urine flow but also the sympathetic-adrenergic system.

1.3 The Urinary Bladder

As a tetrapod innovation, a urinary bladder derived embryologically from the

cloaca, makes its phyletic debut in the Amphibia. It is a distensable sac into which
the urine passes from the cloaca and, in some species, especially those that live
in arid conditions, like the Australian leptodactylid frogs, it can hold fluid equiv-
alent to 50% of the body weight. Townson in 1799 described how frogs "have
power of absorbing the fluids necessary for their support ... through the exter-
nal skin ... a large part of them appearing to be retained in the so-called urinary
bladder, though gradually thrown off again by the skin:' The later experimental
observations of Ewer (1952a) and Sawyer and Schisgall (1956) have shown that
toads and frogs reabsorb water from their urinary bladders when they are dehy-
drated (see also Ruibal1962; Shoemaker 1964}. The urinary bladder of many ter-
restrial amphibians holds large quantities of water compared with more aquatic
species and thus affords them a useful store of water, that can be used to replace
body water at times when other supplies are limited (Bentley 1966}. Such storage
of water may be important for the normal daily activities of more terrestrial
species away from sources of water. It may allow rehydration to occur at intervals
of several days. Stille (1952) observed that toads, Bufo w. fowleri, rehydrated, on
damp beach sand, only every 5 to 6 days. Such stores of water also appear to be
important for the survival of aestivating amphibians.
Before the discovery of vasotocin, mammalian neurohypophysial peptides
were shown, when injected, to increase water reabsorption from the bladders of
toads and frogs (Ewer 1952a; Sawyer and Schisgall 1956). Vasotocin has been
shown to be particularly active in promoting water reabsorption from this organ,
being effective, in vitro, at concentrations of 10- 11 to 10- 12 M (Jard et al. 1960;
Sawyer 1960}. Mesotocin and oxytocin also increase the permeability of the
anuran bladder to water but, in Bufo marin us, they are about 200 times less potent
than vasotocin (Fig. 6.2). This reabsorption of urinary water can supplement
the role of the renal tubule in water conservation. It may also contribute to the
observed antidiuretic effect of vasotocin. In Bufo marinus, the urinary bladder
contributes about 50% of the total urinary water retained in response to injected
vasotocin (Bentley and Ferguson 1967}. In bullfrogs, it is about 20% of the total.
In the fire salamander, water reabsorption from the urinary bladder has been
observed to nearly completely account for the observed "antidiuretic" effect of
vasotocin (Bentley and Heller 1965}. Neurohypophysial peptides increase the per-
meability of the urinary bladder to water in many anurans but not that of the
aquatic toad Xenopus (Bentley 1966}. The response of the urinary bladder of the
euryhaline crab-eating frog is poor (Dicker and Elliott 1966, 1970}. It is also not
very prominent in many urodeles, especially aquatic species (Bentley and Heller
1964; Bentley 1971b). However, urinary bladders of the newt Triturus vitatus,
the salamander Aneides lugubris, the eastern spotted newt Notophthalmus

171
 Sr-----------------------~----~

c
E
~
.....
Cll
E
0
!2

Moles Peptide /I

Fig. 6.2. Water transfer across the urinary bladder (in vitro) of the toad, Bufo marinus, in the
presence of vasotocin (6), oxytocin (e) and mesotocin (0). Note: Log-dose scale. (Bentley
1969a)

viridescens, and the California newt Taricha torosa have been observed to
respond, by increasing water reabsorption, to neurohypophysial peptides
(Warburg 1971; Hillman 1974; Brown and Brown 1980). Large urinary bladders
have been described in caecilians. They probably act as sites for water storage.
However, it is unknown whether they are responsive to vasotocin.

1.4 The Large Intestine (Colon)

The Amphibia have a well-developed large intestine across which sodium is

actively transported (Cooperstein and Hogben 1959). Such transport can result
in the production of osmotic gradients along which water can move. Mammalian
antidiuretic hormone (vasopressin) can increase the osmotic flow of water across
this organ in vitro ( Cofre and Crabbe 1965, 1967), but this effect is very small, an
increase from 3.9J.1lcm- 2 h- 1 to 5J.1lcm- 2 h-I, and is probably not physiologically
significant.
While the neurohypophysis stores and secretes vasotocin, which has multiple
actions related to water metabolism, its precise physiological role is controversial

172
(J0rgenson 1993, 1994, 1997a}. Vasotocin is released into the circulation of
amphibians in response to dehydration, exposure to hyperosmotic solutions
and haemorrhage (Bentley 1969b; Rosenbloom and Fisher 1974; Eggena 1986}. Its
concentrations in the plasma are similar to those in other tetrapods. Neuro-
hypophysectomy is a difficult surgical procedure in amphibians as it is usually
accompanied by damage to the adenohypophysis and it can be incomplete. Pos-
sibly as a result of such problems, clear deficiencies related to water metabolism
have not generally been observed following neurohypophysectomy. In the toad
Bufo marinus, surgical hypothalamic lesions calculated to block the activity of
the neurohypophysis resulted in some deficiencies in their response to dehydra-
tion (Bakker and Bradshaw 1977}. Water uptake across the skin in response to
dehydration and administered hyperosmotic saline were diminished, but not
abolished. An antidiuresis still occurred in the toads with lesions following their
removal from access to water. However, the response was slower in onset than that
of intact toads and it involved only a decrease in GFR. The results were consid-
ered to be consistent with the observations of others, using Rana pipiens and B.
marinus, who attempted to ablate the neurohypophysis (Levinsky and Sawyer
1953; Middler et al. 1967; Shoemaker and Waring 1968). However, neuro-
hypophysectomy in European toads, Bufo bufo, did not result in any detectable
deficiencies in their ability to rehydrate (J0rgenson et al. 1969; J0rgenson 1993).
Possibly sympathetic-adrenergic effects on the kidney and skin are predominant
(J0rgenson 1993). They may also be able to compensate for a deficiency of vaso-
tocin in such circumstances.

2 Salt Exchange

Most amphibians spend extended periods of their lives in fresh water. At least one
species, the crab-eating frog Rana cancrivora is truly euryhaline. Some are pri-
marily aquatic, including tadpoles and larval and neotenous urodeles. Others live
on the banks of rivers, ponds and lakes and are amphibious, entering the water
regularly. Some amphibians lead a more terrestrial existence and only enter water
irregularly, such as to breed and rehydrate. While cavorting in aqueous environ-
ments, exchanges of water and solutes, especially Na+ and cl-, occur continually
across their integument. As described in the previous section, water gained by
osmosis is excreted as dilute urine containing low, but significant, amounts of such
ions. Solute concentration gradients between the body fluids and the external
bathing medium, where the salt concentration may be less than 1 mM, favour a
net loss of salt by diffusion. However, as observed by A. Krogh (Krogh 1937, 1939},
European frogs, Rana esculenta, can survive for many weeks in distilled water.
Only small changes in the salt concentrations of their body fluids were found to
occur. When they are restored to normal pond water, the frogs then accumulate
Na+and Cl- from such solutions by taking it up across their skin. This process can
take place from sodium chloride solutions as dilute as w-sM. It involves active,
metabolically dependent, transport of Na+ and Cl-. Such active Na+ transport was
demonstrated in vitro in the skin of frogs by Ussing and Zerahn in 1951. It has

173
subsequently also been demonstrated in the skin of many other amphibians.
Active Cl- transport, which was demonstrated in vivo (it appears to involve
Cl-/HC0 3- exchange) is not as readily demonstrated in vitro but has been
observed in the skin of some species, such as the South American frog
Leptodactylus ocellatus (Zadunaisky and Candia 1962).
The magnitude of the losses of salts by aquatic amphibians depends on the
permeability of their skin both to ions, and, indirectly, to water. (Excess accumu-
lations of water are excreted as dilute urine with an associated loss of salt.)
Net losses of Na+ and cl-, as a result of diffusion follow their electrochemical
concentration gradients across the skin. The magnitude of such effllux mainly
depends on the special permeability properties of the skin with respect to these
ions. It has been observed that amphibians that habitually live in fresh water have
an integument that has a lower permeability to water and salts than those species
leading amphibious or terrestrial lives (Greenwald 1972; Yorio and Bentley 1978).
In addition, most amphibians can utilize cutaneous ion "pumps" to take up salts
from bathing solutions. Krogh (1939) demonstrated that after keeping frogs in
distilled water for prolonged periods of time, the activity of such ion accumula-
tion mechanisms was enhanced. Maetz and his colleagues (Maetz 1959) also
found such an increase in the activity of Na+transport. They also found that when
the frogs were kept in 0.7% sodium chloride solutions the rate of Na+ transport
by their skin was greatly reduced. Regulatory processes that are sensitive to the
amount of salt in the frogs' environment appear to be present. Evidence for such
a control of salt accumulation across the integument has been observed in many
species of anurans and urodeles and even two species of caecilians (Stiffler et al.
1990). Only sporadic information is available about the nature of such regulation
in vivo but active Na+ transport across amphibian skin can be stimulated in vitro
by aldosterone and vasotocin.

2.1 Skin

Transcutaneous active transport of Na+ has been observed to occur across the
skin of anurans from diverse families, including Ranidae, Bufonidae, Hylidae, Lep-
todactylidae and Pipidae. It has also been demonstrated in many urodeles, includ-
ing the genera Triturus, Salamandra, Ambystoma, Siren and Amphiuma. Such ion
transport also occurs across the integument of the caecilians Typhlonectes com-
pressicauda and Ichthyophis kahtaoensin (Stiffler et al. 1990). Transcutaneous
salt transport does not appear to be present in all amphibians, suggesting that
it is not necessarily essential for their survival. For instance, it is not present
in premetamorphic bullfrog tadpoles (Alvarado and Johnson 1966) or larval tiger
salamanders (Bentley and Baldwin 1980). It is also absent in the mudpuppy
(Bentley and Yorio 1977). However, transcutaneous active Na+ transport can be
promoted in this neotenous urodele by exposing the skin to the amphotericin B.
This drug appears to increase the permeability of the apical plasma membranes
of the cutaneous epithelial cells. Normally in this species, and probably in other
aquatic larval forms, there appears to be a deficiency of sodium channels (ENaC)

174
in the apical plasma membranes of the cutaneous epithelial cells. The promotion
of metamorphic climax in amphibian larvae by thyroid hormone appears to be
associated with the generation or activation of such sodium channels and cuta-
neous Na-K-ATPase. Such larval amphibians presumably maintain their salt
balance by minerals obtained from their diets and by restricting their losses
across the integument and in urine. However, it is also possible that some larval
amphibians utilize their gills for salt accumulation (Alvarado and Moody 1970).
Various zones of the integument of amphibians may exhibit different abilities
to transport salt. Electrical measurements (in vitro) of the "short-circuit current",
which reflects active transcutaneous ion transport (usually of Na+), indicated
that the skin of Xenopus laevis, Ran a pipiens and Bufo marin us exhibited uniform
such activity, but in the tree frog Litoria (Hyla) moorei it was much greater in the
pelvic area (Bentley and Main 1972). Such differences in regional ion transport
have been observed in four other species of tree frogs (Hylidae) (Yorio and
Bentley 1977). This enhanced ion transport appears to be associated with
the pelvic patch area in such species. The pelvic skin of the toad Bufo woodhou-
seii displays a similarly enhanced ability to actively transport Na+ (Baker and
Hillyard 1992). The possible physiological significance of this activity of the
pelvic skin is unknown, but it may reflect morphological differences, such as
skin thickness, which are associated with increased osmotic permeability at such
sites.
Neurohypophysial peptides not only increase the permeability of amphibian
skin to water, but they can also promote an increase in active transcutaneous Na+
transport. Fuhrman and Ussing {1951) demonstrated that mammalian neurohy-
pophysial peptides increase Na+ transport across frog skin (in vitro) and vaso-
tocin has since been shown to be even more effective (Jard et al. 1960; Maetz 1963).
This action of these peptides on Na+ transport (the natriferic effect) has been
demonstrated in a number of anurans including Rana esculenta, R. catesbeiana,
Bufo bufo, B. marinus and Xenopus laevis (Maetz 1963; Bentley 1969a). It does
not occur in R. catesbeiana tadpoles (Alvarado and Johnson 1966). A natriferic
response has also been observed in several urodeles, including Triturus alpestris,
T. cristatus (Bentley and Heller 1964), Ambystoma mexicanum (Aceves et al.
1968), Aneides lugubris (Hillman 1974) and adult Ambystoma tigrinum (Bentley
and Baldwin 1980). It has not been observed in larval A. tigrinum (Bentley and
Baldwin 1980) or the neotenous urodeles Amphiuma means, Siren lacertina
(Bentley 1975) or Necturus maculosus (Bentley and Yorio 1977). The natriferic
effect of neurohypophysial peptides is not invariably associated with the increase
in water permeability (the hydrosmotic response) that these peptides can also
induce. Thus, in the mudpuppy there is a small hydrosmotic response but no
natriferic response (Bentley and Yorio 1977). The newt Triturus alpestris exhibits
a natriferic response to vasotocin but there is no detectable hydrosmotic effect
(Bentley and Heller 1964). The two responses involve different effector mecha-
nisms; ENaC channels for the natriferic response and, presumably, an aquaporin
for the hydrosmotic response (see Chap. 2). It is unknown if the natriferic effect
of vasotocin on amphibian skin has any physiological significance. Compared to
the actions of aldosterone (see below), this effect of vasotocin is quite transitory.
The conditions for the release of vasotocin are also inappropriate for a role in

175
sodium homeostasis. (Release is inhibited by hyposmotic conditions such as
would be expected to occur during sodium deficiency.) Possibly, it makes a local-
ized contribution to the functioning of the skin such as could involve mainte-
nance of its permeability and sensory processes that utilize electrical signals. The
latter could be important for the detection of salts in the external medium and
the selection, during dehydration, of a suitable solution for "cutaneous drinking"
(see later).
Aldosterone is secreted by amphibians, as in other tetrapods, in response to a
depletion of sodium in the body. This effect has been observed in toads (Crabbe
1961a; Garland and Henderson 1975) and larval tiger salamanders (Stiffler et al.
1986). Conversely, elevated concentrations of Na+ in their bathing media depress
the levels of aldosterone in the plasma. Adrenocorticosteroids, including aldos-
terone, have well-defined and persistent effects in stimulating active Na+ trans-
port, in vitro, across the skin of frogs and toads (Taubenhaus et al. 1956; Maetz
1959; McAfee and Locke 1961; Crabbe 1964; Crabbe and De Weer 1964; Yorio and
Bentley 1978). Injected aldosterone increases the uptake of Na+ by larval tiger sala-
manders (Alvarado and Kirschner 1963). A physiological role for aldosterone in
promoting Na+ uptake across the skin of amphibians does not appear to be in
doubt, though its precise quantitative contribution is uncertain.
Amphibian skin has a sympathetic-adrenergic innervation that supplies
mucous glands and blood vessels, and may influence the permeability and ion
transport activities of its epithelial cells (Castillo and Orci 1997). Adrenaline pro-
motes a loss of cl- from frog skin by stimulating secretion by mucous glands
(Koefoed-Johnsen et al. 1952). This response has been observed in a variety of
anurans (Castillo and Orci 1997). Noradrenaline has also been found to stimulate
Na+ transport across frog skin in vitro (Bastide and Jard 1968; Watlington 1968).
These effects of catecholamines appear to be principally 13-adrenergic ones. The
secretory response of the mucous glands may be important in maintaining the
hydration of the skin in terrestrial environments. However, the consequences of
the various cutaneous actions of catecholamines on the amphibian's salt metab-
olism are unknown.
Insulin has been shown, in vitro, to increase active Na+ transport across the
skin of Bufo marinus (Andre and Crabbe 1966). Its action appears to be syner-
gistic with that of aldosterone. It is unknown whether this effect reflects a normal
physiological interaction between the two hormones in vivo.
Prolactin has been observed to influence the permeability of the skin of urode-
les, which is reminiscent of its action on the gills of teleost fish (see Chap. 7 ). Its
general effect, which is seen in larval and neotenous amphibians, appears to
involve a reduction in permeability to water and salt (Brown and Brown 1987).
Pang and Sawyer (1974) observed that hypophysectomy results in large losses of
Na+ across the integument of mudpuppies. This deficiency could be corrected by
the administration of prolactin. The injection of prolactin into the newt Triturus
cristatus during its terrestrial phase results in a decline in osmotic permeability
and Na+ transport across their skin (Lodi et al. 1982). These conditions were nor-
mally observed in the newts when they were in their aquatic phase. In the newt
Notophthalmus (Triturus) viridescens, long-term treatment with prolactin has
been observed to increase the thickness of the skin and decrease its permeabil-

176
ity to water and Na+ (Brown and Brown 1973). An electrical analysis of the per-
meability of the skin of the Japanese newt Cynops pyrrhogaster demonstrated that
prolactin could block Na+ transport channels (ENaC ?) (Takada and Shomazaki
1988). Prolactin may have a special role in the adaptation of the skin of urodeles
to aquatic life.

2.2 The Kidney

The urine of amphibians kept in fresh water contains little salt. Thus, the ureteral
urine from Rana esculenta living in fresh water contains only about 5 mEql- 1
sodium (Jard and Morel 1963) while in urodeles, such as Triturus, the sodium
levels in the bladder urine are similar to this. Analysis of the glomerular filtrate
obtained by micropuncture of the renal tubules indicates that sodium and
chloride are progressively reabsorbed as they pass down the nephron, this occur-
ring mainly in the proximal, but also in the distal, segment (Walker et al. 1937).
When euryhaline green toads, Bufo viridis, are acclimated to hyperosmotic
bathing media containing 115 and 250mEql- 1 sodium chloride, they initially
accumulate salt (ShPun and Katz 1995, 1999). The subsequent urine flow and renal
clearances of Na+ and cl- were related to the concentration of salt present in
the external solution. The GFR was similar in the toads in either solution. Salt
excretion was regulated by changes in the renal tubular reabsorption of salt. The
kidneys of the toads contributed "efficiently" to regulation of the ions in such
media.
The role of hormones in regulating these processes in amphibians is not clear.
While from the mammalian evidence it seems likely that corticosteroids influence
sodium reabsorption and potassium excretion, this has not been directly shown
in frogs and toads. Injections of aldosterone into Bufo marinus have no consis-
tent effect on renal sodium losses (Middler et al. 1969). Mayer (1963, 1969) also
found this to be so in Rana esculenta. When larval tiger salamanders are adapted
to an external medium of distilled water or 150 mEq 1- 1 sodium chloride, the
concentrations of salt in the urine, respectively, decline or increase (Stiffler et al.
1986). The concentration of aldosterone in the plasma was found to be six-fold
higher and corticosterone was 45% greater when the salamanders were kept in
the distilled water as compared to normal pond water. In the salt solution the
plasma aldosterone concentration was depressed by 47%. The correlation
between urine Na+ levels and the aldosterone in the plasma of the salamanders
suggested that the hormone was increasing renal tubular reabsorption of salt. It
has also been observed that administration of the drug aminoglutethimide, which
reduces synthesis of adrenocorticosteroids (chemical adrenalectomy), decreased
the renal tubular reabsorption of Na+ (Heney and Stiffler 1983). The failure to
demonstrate direct effects of aldosterone on renal tubular Na+ reabsorption in
anurans is vexing.
Vasotocin increases sodium reabsorption by the renal tubule of Rana esculenta
(Jard and Morel 1963; Jard 1966), an observation similar to that of the action of
ADH in the mammalian renal tubule. As described earlier (Chap. 1), this response

177
in mammals may contribute to the maintenance of the renal medullary solute
concentration gradient that is necessary for the formation of hyperosmotic
urine. Amphibians lack the necessary renal morphology for such a process, but
the natriferic tubular response is present. Whether it normally contributes
to renal Na+ conservation in amphibians or is merely a "preadaptation" is
unknown.
Natriuretic pep tides, ANP, BNP and CNP, have been identified in the Amphibia.
Their actions have been studied in bullfrogs, Rana catesbeiana, toads, Bufo
marinus and Xenopus laevis. Their effects are similar to those that have
been observed in mammals, but the precise mechanisms mediating the responses
may differ. In bullfrogs, several natriuretic peptides had a vasodilatatory action,
reduced the force of contraction of the heart and decreased blood pressure
(Uchiyama et al. 1997). Frog ANP was found, in vitro, to induce a diuresis
and natriuresis in the kidney of Bufo marinus (Meier and Donald 1997}. Specific
binding sites, probably receptors, for natriuretic peptides have been identified
in the glomeruli of Xenopus laevis and Bufo marinus (Kloas and Hanke 1992;
Meier and Donald 1997}. (Such binding sites were also identified in the toad
urinary bladder.) Cyclic GMP mediates the effects of natriuretic peptides.
Increases in its concentration in response to the presence of natriuretic peptides
have been observed in preparations of the glomeruli, but not the renal tubules,
of bullfrogs (Uchiyama et al. 1997}. The action of natriuretic peptides on the
amphibian kidney appears to involve actions on the glomerulus. At this time
it would appear that a renal tubular response, which is seen in mammals, is
absent.

2.3 The Urinary Bladder

The urinary bladder of the Amphibia, in addition to performing the function of

a water reservoir, can decrease the sodium content of the urine. Active sodium
transport has been shown (in vitro) to take place across the urinary bladders of
frogs, Rana esculenta, and toads, Bufo marinus (Leaf et al. 1958).
Sodium transport across the urinary bladders of Bufo marin us and Rana ridi-
bunda is increased by aldosterone, either when the animals are injected 24 h prior
to measuring sodium transport in vitro, or after the tissue is directly exposed to
the steroid's action (Crabbe, 1961b,a; 1963). Other steroids, including corticos-
terone, are not as active, and at veryhigh concentrations {100 times as great) may
inhibit its action. Changes in the sodium concentration of the media bathing the
toads influences the rate of sodium transport across the bladder in a manner that
parallels that of aldosterone in the blood; a low external sodium level increases
aldosterone in the blood and stimulates sodium transport.
Leaf et al. {1958) found that oxytocin increases sodium transport across the
toad urinary bladder and vasotocin has been found to be very active in this
process in frogs {Jard et al. 1960}. In Bufo marinus vasotocin is about 100 times
more active in increasing sodium transfer across the bladder than either oxytocin
or mesotocin (Fig. 6.3).

178
 Moles Peptide/ 1

Fig. 6.3. Sodium transfer (as short-circuit current) across the urinary bladder (in vitro) of the
toad Bufo marinus in the presence of vasotocin (L:::.), oxytocin (e) and mesotocin (0 ). Note:
log-dose scale. (Bentley 1969a)

As in the anuran skin, several other hormone preparations have been shown
to promote sodium transport across the bladder. These include insulin (Herrera
1965) and adrenaline (Jard et al. 1968). Various endocrine factors may interact in
their effects on the bladder. Aldosterone can facilitate the effects of neurohy-
pophysial peptides (Fanestil et al. 1967; Handler et al. 1969). Aldosterone and
insulin, similarly, together can produce a far greater increase in sodium transport
in vitro than either can produce alone (Crabbe and Francois 1967). Such syner-
gistic endocrine interactions probably assist such ussues to attain optimal levels
of sodium transport.
The urinary bladder is the site of Na+ reabsorption in several urodele amphib-
ians, including Necturus maculosus, Ambystoma tigrinum, Amphiuma means and
Siren lacertina (Bentley and Heller 1964; Bentley 1973a). This process, measured
in vitro as the electrical short-circuit current, which could be inhibited by
amloride, was usually unresponsive to vasotocin and aldosterone. However, these
amphibians were all maintained in dilute solutions, which are conditions when
the endogenous concentrations of aldosterone in the plasma, and Na+ transport
would already be expected to be high (Stiffler et al. 1986). Responses to exoge-
nous aldosterone may then be suppressed. Aldosterone, when preinjected into
Necturus, increased the short-circuit current across its urinary bladder (measured
in vitro) (Bentley 1971b).
Sodium reabsorption from urine stored in the urinary bladders of amphibians
may contribute to the conservation of this ion in many species. It appears to be
acting as a functional extension of the distal renal tubule and, as in the kidney of
many tetrapods, can utilize aldosterone to control this process.

179
2.4 The Large Intestine (Colon)

Sodium is actively transported from the mucosal to serosal side of the colon in
anurans (Cooperstein and Hogben 1959). In the toad, Bufo marinus, this process
can be increased by aldosterone and neurohypophysial peptides ( Cofrt~ and
Crabbe 1965, 1967).
Aldosterone has been identified in the plasma of several amphibians and its
release occurs under conditions of a sodium deficiency. This adrenocorticosteroid
exhibits a typical mineralocorticoid action, which is absent in fishes, but present
in other tetrapod vertebrates. In amphibians an important target tissue is their
permeable skin. The colon and urinary bladder are additional sites of its action,
and these tissues are similarly responsive in other tetrapods. However, it is not
clear whether a renal response to aldosterone is widespread in amphibians. The
overall contribution of aldosterone to sodium and potassium metabolism in
amphibians is not clear. Adrenalectomy is a difficult operation in such animals
and reported attempts to perform this procedure are sparse. The results are com-
plicated by the simultaneous loss of the glucocorticoid action of corticosterone.
The toad Bufo arenarum has been shown to suffer an excessive loss of salt fol-
lowing adrenalectomy (Marenzi and Fustinoni 1938). Fowler and Chester Jones
(1955) destroyed the adrenocortical tissue in the frog Rana temporaria. In
summer, the frogs died within 2 days, although in winter they survived for
prolonged periods of time. The summer frogs lost large amounts of Na+ and
accumulated K+. This response is what occurs in mammals suffering from adreno-
cortical deficiency. When the summer frogs were placed in isosmotic saline they
survived longer, which suggests that their demise was due to faulty electrolyte
balance (Chester Jones et al. 1959). The site, or sites, of the excessive Na+ loss in
the adrenalectomized frogs was not determined. In larval tiger salamanders,
chemical adrenalectomy with the drug aminoglutethimide resulted in a decline
in the concentration of Na+ in the plasma and increased its excretion in urine
(Heney and Stiffler 1983). This deficiency could be corrected by the administra-
tion of aldosterone or, in larger doses, corticosterone.
The synthesis of aldosterone in amphibians is under the control of both ACTH
and the renin-angiotensin system (Du Pont et al. 1976; De Ruyter and Stiffler
1986). Adenohypophysectomy in Bufo marinus results in an excessive loss of
Na+ that did not appear to involve kidney function (Middler et al. 1969). This
salt loss could be prevented by the administration of ACTH. Hypophysectomy in
the newt Triturus cristatus also resulted in an excessive loss of Na+ (Peyrot et al.
1963). The synthesis of corticosterone is also regulated by ACTH and its loss
following hypophysectomy complicates the interpretation of such experiments.
Nevertheless, the available evidence supports the view that the adrenocorticos-
teroids, especially aldosterone, play an important role in the osmoregulation of
the Amphibia.

180
3 Nitrogen Metabolism

The main catabolic end products resulting from the deamination of amino acids
can be ammonia, urea or uric acid (see Chap. 1). They all require water for their
excretion. Ammonia, which is quite toxic, is the principal such excretory product
of ammonotelic animals, including aquatic amphibians such as Xenopus laevis
and the mudpuppy. Ammonotelic amphibians can often also form urea, but in
their normal aquatic conditions ammonia is predominant. The ammonia is prin-
cipally excreted across the skin into the surrounding water. Terrestrial amphib-
ians, with limited access to water, usually utilize urea as the main end product of
nitrogen metabolism. It is mainly excreted in the urine. A few arboreal frogs can
convert catabolic nitrogen to uric acid, which is also excreted in the urine.
However, it requires less water for this process than urea.
Urea has a relatively low toxicity and can, under various circumstances, be
accumulated in high concentrations in the tissue fluids of amphibians (see Wright
1995; J0rgenson 1997b; Withers 1998b). In euryhaline species, such as Rana can-
crivora and Bufo viridis, urea can be utilized as a "balancing osmolyte". It helps
maintain the concentrations of the body fluids at levels that are slightly hyperos-
motic to those of the external saline media (Gordon et al.1961; Gordon 1962; Katz
1973). This osmotic strategy is also used by marine elasmobranchs. These fish also
accumulate other solutes, such as trimethylamine oxide, which reduce the poten-
tial toxic effects of high concentrations of urea. However, amphibians appear to
be even more tolerant to urea than elasmobranchs, and do not appear to resort
to this strategy (Withers and Guppy 1996). Aestivating amphibians, such as the
desert spadefoot toad Scaphiopus couchi (McClanahan 1967) and the urodele
Siren lacertina (Etheridge 1990), also accumulate urea. Concentrations of urea as
high as 900 mM have been observed in the plasma of the toads. In these circum-
stances it acts as a "storage osmolyte" which is subsequently excreted in the urine
when adequate water becomes available.
Urea synthesis and excretion may be regulated in response to the amphibian's
current needs. Xenopus laevis in their normal aquatic environment are am-
monotelic. They periodically aestivate, in the mud, when the pools where they
live dry up. The aestivating toads accumulate urea at high concentrations in their
body fluids (Balinsky et al. 1967). This metabolic change is associated with an
increase in the levels of the liver enzyme carbamoylphosphate synthetase that
directs ammonia into the ornithine-urea cycle (see Fig. 1.5). This response may
be a direct result of the toxicity of rising levels of ammonia in the body or a con-
sequence of dehydration. Such increases in the ureogenic activity of the hepatic
ornithine-urea cycle occur in other amphibians, including Scaphiopus couchi,
Bufo viridis and Rana cancrivora. Such adaptation is not associated with changes
in oxygen consumption. However, increases in urea synthesis may also be
favoured by a shift to protein catabolism, as observed in Scaphiopus (Jones 1980)
and a stimulation of gluconeogenesis, as seen in Bufo viridis (Hoffman and Katz
1998). Adrenocorticosteroids promote gluconeogenesis and mobilization of tissue
proteins in vertebrates, but there appears to be no information about this hor-
monal response in such amphibians (Jungreis 1976).

181
 Renal retention of urea provides an important mechanism for its conservation
in Rana cancrivora (Schmidt-Nielsen and Lee 1962) and Bufo viridis (ShPun and
Katz 1995). Urea excretion by the kidneys in many amphibians is influenced by
the GFR and its secretion by renal tubule (Forster 1954). However, in anurans
which utilize urea as a balancing osmolyte, urea appears to be mainly conserved
by its tubular reabsorption (Carlisky et al. 1968; Schmidt-Nielsen and Lee 1962).
Urea can also be reabsorbed across the urinary bladder of the toad Bufo marin us
and this process can be increased, in vitro, by neurohypophysial peptides (Leaf
and Hays 1962). Vasotocin has been observed to increase urea absorption, in vitro,
across the urinary bladder of the crab-eating frog (Dicker and Elliott 1973). It
may be contributing to urea conservation by this euryhaline frog. The adminis-
tration of ACTH, corticosterone and aldosterone increases plasma urea concen-
tration in neotenic Mexican axolotls (Ambystoma mexicanum) (Schultheiss 1977).
It was suggested that a decreased excretion of urea could be contributing to
this effect. Increased protein utilization due to a gluconeogenic effect of the
adrenocorticosteroids could also be involved. Amphibian skin is permeable to
urea, and neurohypophysial peptides can increase this process (Andersen and
Ussing 1957). The magnitude of this response to vasotocin varies in different
species (Yorio and Bentley 1978). It could provide an extrarenal avenue for urea
excretion in aquatic conditions such as could be utilized during rehydration
following aestivation.
Uricotelism has been observed in frogs of the genus Chiromantis (family
Rhacophoridae) that live in Africa (Loveridge 1970; Drewes et al. 1977) and
Phyllomedusa (Hylidae) from South America (Shoemaker et al.1972a). These tree
frogs live, without access to water, in dry exposed situations for prolonged periods
of time. They reduce their evaporative water loss by waterproofing their skin.
Their uricotelism would be expected to further reduce their need for water. Until
the discovery of these amphibians, it had been generally assumed that the use of
uric acid as a method for disposing of catabolic nitrogen had first evolved in
reptiles. Campbell and his colleagues (1987) have suggested that uricotelism
probably arose in an amniotic amphibian ancestor of the reptiles. However, it
seems doubtful that these extant frogs are relicts of such an ancestry. They prob-
ably reflect separate evolutionary origins of this important biochemical process.

4 Reproduction

The Amphibia, in contrast to other tetrapods, produce anamniotic eggs which lack
a shell. Such non-cleidoic, fish-like eggs generally must be deposited in water. Fer-
tilization is usually external. Thus, even terrestrial amphibians generally need to
return to water to breed. However, a few frogs and urodeles, and most caecilians,
can retain eggs in the oviduct, where they undergo a period of gestation (Wake
1993 ). In anurans and urodeles such ovoviviparous and viviparous species usually
live in cool alpine areas. This reproductive strategy can thus be viewed as an adap-
tation to cold. However, as will be described below, at least one such frog lives in
hot deserts, and all the caecilians inhabit hot tropical regions.

182
 The aquatic larvae of amphibians, on hatching, undergo a period of growth
and differentiation before undergoing metamorphosis to a juvenile adult form.
Some frogs, such as the Australian leptodacylids and myobatrachids, deposit their
eggs in damp soil at the bottom of deep burrows (Main et al. 1959; Roberts 1981,
1984). They emerge from this seclusion, as juveniles, following rain. The eggs of
some such frogs are enclosed in a gelatinous capsule. Other amphibians are ovo-
viviparous or are even considered to be viviparous. Species that live in dry desert
conditions utilize various such methods of reproduction, but most are conven-
tional and, following rain, seek out ephemeral ponds and pools.
The amphibian reproductive cycle, like that in other vertebrates, is controlled
by the hypothalamic-pituitary-gonadal axis of hormones (Lofts 1984). Environ-
mental temperature and rainfall, rather than light, appear to be the principal
external stimuli that influence their reproduction. In areas with predictable
weather, reproduction is seasonal, and may also involve internal physiological
rhythms. However, in dry regions, such as occur over much of Australia, the
trigger to reproduce may be the occurrence of rain. Such "opportunistic" breed-
ing also occurs in Australian birds. The frogs appear to achieve a "tonic" repro-
ductive condition so that ovulation, oviposition and spermiation can occur
rapidly, sometimes within hours of rain falling. It has been observed that the
oviduct of amphibians can contract in response to the presence of vasotocin
(Heller 1972), and this hormone could be involved in such oviposition.
Preparative reproductive behaviour and migration to water to breed (water
drive) can be promoted in the eastern spotted newt Notophthalmus viridescens
by the administration of prolactin (Reinke and Chadwick 1939; Chadwick 1940,
1941). This effect has been observed in other newts including Triturus cristatus,
T. alpestris (Tuchmann-Duplessis 1948; Giorgio et al.1982) and the Japanese newt
Cynops pyrrhogaster (Toyoda et al. 1996). The actions of prolactin, as described
earlier, also include morphological changes in the structure and osmotic proper-
ties of the skin, which are consistent with the adoption of aquatic life. Sexual
behaviour in male rough-skinned newts, Taricha granulosa, can be stimulated by
the administration of vasotocin (Zoeller and Moore 1988). However, this effect
appears to be distinct from its actions on osmoregulation and involves local
actions in areas of the brain concerned with sexual behaviour.
Premetamorphic larval development in amphibians is assisted by the activities
of the hypothalamo-pituitary-thyroid axis, prolactin and, possibly, adrenocorti-
costeroids. Thyroid activity is low in early premetamorphic life, during which
growth is promoted and metamorphosis is inhibited by prolactin (Dickoff 1993).
Metamorphic climax is precipitated by rising levels of thyroid hormone in asso-
ciation with thyroid-stimulating hormone and hypothalamic TRH. The nature of
the involvement of adrenocorticosteroids is not clear. They may contribute to the
activity of thyroid hormone by enhancing the formation of triiodothyronine from
thyroxine and decreasing its inactivation (Galton 1990). The period of larval life
in anurans can vary from about 7 days in spadefoot toads living in the desert to
3 years in bullfrogs from colder regions in North America. A more usual period
of premetamorphic development in spadefoot toads is 30 to 40 days (Warburg
1997). A longer premetamorphic period usually results in larger juveniles, which
are better able to withstand life stresses, including desiccating conditions.

183
However, metamorphosis sometimes appears to be "facultative" and may depend
on conditions in the pond, including the food supply, pH and solute concentra-
tions. Such limnological circumstances may impinge on the hormonal processes
regulating metamorphosis. There is little information about this possibility.
The West African viviparous frog Nectophrynoides occidentalis aestivates in
burrows during periods of seasonal drought. Fertilization usually occurs in
October and drought conditions commence in November. The development of the
larvae in the oviduct is suppressed during aestivation by the secretion of proges-
terone from the ovary (Xavier and Ozon 1971; Xavier 1974). The frogs emerge the
following April and larval development continues until June. This interesting
strategy of an amphibian to adapt its reproduction to drought conditions appears
to be unique.
The larvae of some urodeles, such as the tiger salamander, achieve a size that
is similar to that of the adults. A number of other urodeles are neotenous and
retain the larval form, including external gills. They are paedomorphic and can
reproduce. These amphibians include mudpuppies, mud eels, congo eels and the
Mexican axolotl. The latter can even be artificially induced to metamorphose by
administering thyroid hormone. The integument of such urodeles, as described
earlier, generally exhibits a lower osmotic and ion permeability than adults and
a reduced or lack of response to vasotocin. Such properties of their integument
are similar to those of anuran tadpoles. As metamorphosis becomes imminent,
the skin of tadpoles begins to behave more like that of adults and displays active
transcutaneous Na+ transport (Taylor and Barker 1965; Cox and Alvarado 1983).
One of the changes that takes place at metamorphosis is an increase in the levels
of Na-K-ATPase (Taylor and Barker 1965) and the appearance of epithelial
sodium channels (ENaC). An ability to respond to vasotocin also develops.

S Accumulation of Water and Salt

Most amphibians are carnivorous, principally consuming invertebrates, though

some, such as large cane toads, sometimes even eat small mammals. Such a diet
can be expected to meet their normal need for salt, probably even when they
lead an exclusively aquatic existence. However, the water contained in such a
diet appears to be inadequate for the total needs of most terrestrial amphibians.
Feeding may be sporadic in some amphibians, and in aquatic species and those
that hibernate under water it is possible that their ability to accumulate Na+ and
cl- across their skin could be a physiological necessity.
It is generally accepted that amphibians do not drink in order to rehydrate
(Adolph 1933; Bentley and Yorio 1979). Instead, they absorb water osmotically
across their permeable skin. The tadpoles of the crab-eating frog may be an excep-
tion, as they drink the brackish water in which they live and, as occurs in teleost
fish, apparently excrete the salt across their gills (Gordon and Tucker 1965).
Aquatic amphibians, such as the urodeles Amphiuma means and Siren lacertina,
normally imbibe small amounts of the water in which they live (Bentley 1973a).
Frogs may be induced to swallow even unpalatable salt solutions when exposed

184
to severe stress (Krogh 1939; Bentley and Schmidt-Nielsen 1971). However,
normal rehydration occurs by absorption in what has been called cutaneous
drinking. As described above, the rate of such water absorption in response to
dehydration is a process that is increased by vasotocin. There are differences in
the speed of such rehydration in various amphibians. It often occurs across a spe-
cialized area of the integument called the pelvic patch that is well vascularized
and very responsive to vasotocin (see above). Amphibians have been observed to
periodically migrate and search for suitably damp surfaces from which to absorb
water (Stille 1952; Brekke et al. 1991). Some even appear to exhibit "anticipatory
cutaneous drinking" prior to any measurable dehydration (J0rgensen 1994).
Mammals, birds and reptiles utilize the renin-angiotensin system to induce
thirst in response to decreases in the volume of the body fluids. As described
above, a resulting formation of angiotensin II stimulates thirst receptors associ-
ated with the hypothalamus and induces drinking behaviour. Attempts to induce
such drinking by the administration of angiotensin II has not been successful in
any amphibians (Kobayashi et al. 1979; Kobayashi and Takei 1997). However, von
Sechendorff Hoff and Hillyard in 1991 made the fascinating observation that
when red-spotted toads, Bufo punctatus, were injected with angiotensin II they
exhibited prolonged "water-seeking behaviour." This involved persistent apposi-
tion of their pelvic patch region to proffered damp surfaces of soil. There was a
resulting water uptake. This water absorption response (WR) could be inhibited
by the prior injection of the angiotensin II antagonist drug saralasin. The injec-
tion of angiotensin II into the brain also promoted the water-absorption response
(Propper et al. 1995). Amphibians appear to utilize a hormonal mechanism to
promote cutaneous rehydration behaviour that parallels the effects of angiotensin
II on thirst and oral drinking in other tetrapods (Hillyard et al. 1998).
Angiotensin II also has a vasoconstrictor effect and can increase blood pres-
sure and the release of aldosterone. Optimal osmotic water transfer across the
pelvic patch of amphibians depends on an adequate blood flow in the region of
the pelvic patch. Captopril, a drug which blocks the conversion of angiotensin I
to II, can inhibit water absorption across the pelvic patch of dehydrated toads
and decreases the blood pressure (McDevitt et al. 1995). It was suggested that
angiotensin II may facilitate water absorption across the pelvic patch by
maintaining blood pressure during dehydration. Aldosterone has been observed
to reduce the threshold when dehydration evokes water-seeking behaviour in
green toads (Hoffman and Katz 1999). The authors suggested that angiotensin II
and aldosterone increase the frequency of water-seeking behaviour while vaso-
tocin subsequently promotes water uptake across the pelvic patch. However,
as just described, angiotensin II may also contribute to the latter response.
Aldosterone appears to act only in the initial water-seeking phase. The nature
of this adrenocorticosteroids action is unknown, but it clearly merits further
investigation.
The search for "potable" water by toads is a discriminating one (Stille 1952;
Brekke et al. 1991; Hillyard et al. 1998). They appear to utilize the skin on their
feet and ventral surface to "taste" the water. When they locate a damp surface,
toads have been observed to exhibit "seat-patch-down" behaviour when they
briefly explore its suitability for cutaneous absorption. They appear to be able to

185
discriminate between the concentrations of such solutions as sodium chloride,
potassium chloride and urea. Their sodium taste appears to be related to the rate
ofNa+ transport across the skin (von Seckendorff Hoff and Hillyard 1993}. When
this process is blocked by the drug amiloride, they lose the ability to taste solu-
tions of sodium chloride. The activity of taste bud cells in the mammalian tongue
can also be blocked by amiloride. The enhanced rate of Na+ transport, which has
been observed in the pelvic patch of anurans and which can be further stimu-
lated by vasotocin, may be contributing to such a cutaneous sense of taste.
Apart from accumulating salt from their diets, amphibians can take up Na+and
Cl+ across their skin from solutions as dilute as w-s M. The ability of the skin to
limit losses of such ions from the body fluids is not in doubt. However, the phys-
iological importance of skin as a conduit for salt accumulation is not clear. Krogh
in 1939 remarked that "it (cutaneous salt uptake) may be of vital importance to
the frogs in winter when about 7 months are spent under water without food".
He (Krogh 1937} maintained fasting European frogs in distilled water, which was
constantly changed, for periods of up to 12 months. Most survived, but they dis-
played a slow decline in serum Ct concentrations. In 1972, McAfee repeated these
experiments using North American leopard frogs (Rana pipiens) and over a
period of 60 days could not detect any change in the concentration of Na+ in the
plasma or the whole body content of this ion. I maintained three species of
anurans (Rana pipiens, Bufo marin us and Xenopus laevis) for 15 days in tap water
containing 0.25mEql- 1 Na+ and amiloride (10-5 M) (Bentley 1973b). The latter
drug blocks the transcutaneous uptake of Na+. There was a small decline in the
serum Na+ concentration in the B. marinus, but no significant change in the levels
of this ion in the other two species. The skin of B. marin us subsequently displayed
what appeared to be a compensatory increase in transcutaneous Na-dependent
short-circuit current. Such a change was not observed in the behaviour of skin
from the other two species. It should be recalled that B. marin us normally lives a
mainly terrestrial life, while R. pipiens is amphibious and X. laevis is completely
aquatic. Prolonged exposure to distilled water can result in a rise in the concen-
trations of aldosterone in the plasma in amphibians. This hormone is probably
mediating the increased salt transport in B. marinus. The affinity constant (Km)
for the transcutaneous Na+ transport has been observed to be lower in aquatic as
compared to more terrestrial species of amphibians (Greenwald 1972}. Possibly
this difference reflects an adaptation of this process to life in a salt-poor envi-
ronment. However, on a short-term basis, the importance of such a mechanism
for the accumulation of salt is questionable, except in amphibians hibernating
under water. Active transport of Na+ occurs across many epithelial membranes.
Not all of these are primarily concerned with the accumulation of salt. The process
may have other roles, including the maintenance of the integrity of epithelium
itself, the cotransport or exchange of other solutes, acid-base balance and even
participation in sensory processes. The active transport of Na+ across the skin
appears to be important for the accumulation of salt in some, but probably not
all, amphibians.

186
Chapter 7

The Fishes

The fishes, or Pisces, are aquatic vertebrates that breathe with the aid of gills. They
are thought to have originated 500 million years ago, a time that predates the
origin of tetrapods by some 200 million years. It is uncertain whether the trans-
formation from an invertebrate ancester took place in fresh water or in the sea,
but subsequently, fish have adopted both of these environments, as well as inland
lakes and springs where the solute concentrations of the waters may even exceed
those in the sea. The Pisces contains about 23 000 species, more than all of
the tetrapods, which occur in several widely divergent evolutionary classes. The
principal of these are: (see Table 1.1) the Agnatha (the jawless lampreys and the
hagfishes), the Chondrichthyes (sharks, rays and chimaeras) and the Osteichthyes
(bony fishes). The teleostean fishes, which are a group of the latter bony fish, are
today the predominant group in both fresh water and the sea; there is more infor-
mation about the physiology of these than for the other classes of fish. From the
biological viewpoint, however, further information about osmoregulation in the
sparser relict fishes would probably be even more interesting, especially as it could
aid our understanding of the evolution of osmoregulation in vertebrates. Such
archaic fish include the lungfishes, the coelacanth, the sturgeons, the bowfin and
garpike, and the lampreys and hagfishes. At present, physiological information
about these fishes is somewhat limited.
The sharks and rays and the bony fishes probably originated in the sea (see
Halstead 1985), but they have subsequently migrated into fresh water. While con-
temporary species of some of the main orders within these groups of fish may
today live solely in fresh water (the lungfishes and bichir) or the sea (the co-
elacanth), in the course of geological time some representatives of all such
evolutionary divisions have occupied both habitats (see Darlington 1957). The
dominant teleosts are thought to have originated in the sea, but some sub-
sequently moved into fresh water and a number of these have even returned to
the sea. Darlington ( 1957) gives a fascinating description of the dispersal of fresh-
water fishes throughout the world, and this has often involved several successive
migrations between the sea and fresh water. The freshwater catfishes of Australia,
for instance, moved into the antipodean rivers from the sea, but their immediate
marine ancestors previously originated from freshwater ancestors that probably
lived in Asia. When one considers the complexities of such transformations, it is
not surprising to find considerable diversity in the detailed pattern of osmoreg-
ulation of fishes, though the basic blueprint remains remarkably uniform.
Most contemporary species of fish have only a limited ability to move between
fresh water and salt solutions like sea-water. Such osmotically conservative fishes
are stenohaline, while others, which can adapt more readily to either type of

187
solution are euryhaline. As emphasized by Fontaine and Koch (1950), such a
classification is not rigid, some fish being "more or less" stenohaline while others
are "more or less" euryhaline. Thus, the freshwater goldfish and the marine perch
can both live in salt solutions about one-third the concentration of the sea (Lahlou
et al. 1969a; Motais et al. 1966). Some euryhaline fishes can withstand direct
transfer from fresh water to sea-water, while others, such as the lamprey, once
having migrated into rivers, will die if they are then replaced in the sea (Hardisty
1956; Morris 1960). Euryhaline fishes are often migratory breeders; some, like
lampreys and salmon, move from the sea into rivers, where they produce their
eggs, while others, like the eel, return to the sea to breed. Many euryhaline fishes
occupy estuaries and certain inland lakes and streams where the salinity may vary
considerably during different seasons. The osmotic adjustments which must be
made by such fishes would seem to offer a situation for endocrine coordination.
In natural conditions, adaptation to solutions of differing osmotic concentration
probably can take place gradually, as when such water is evaporated from an
inland lake or fish migrate through estuarine areas between rivers and the sea
(Fontaine and Koch 1950). Such situations would seem to be particularly suitable
to the relatively long-term actions that are characteristic of many hormones.
Fish can live in solutions with a wide range of osmotic concentration. As
described above, fish that normally live in the sea or fresh water can often toler-
ate solutions of intermediate concentration. Others can live in waters with a solute
concentration considerably higher than that of sea-water; Oreochromis mossam-
bica may survive in a salinity of 6.9%, while the cyprinodont Cyprinodon varie-
gatus has been found in saline waters with a concentration of 14.2% (see Parry
1966). Such osmotic tolerance presumably constitutes a rather special physiolog-
ical adaptability about which we have little knowledge.
Fishes contain an amount of water that is equivalent to 70 to 75% of their body
weight, which is similar to the water content of most other vertebrates. The dis-
tribution of this water in the body varies somewhat in different species (Thorson
1961). The plasma volume of agnathans and chondrichthyeans constitutes about
5% of their body weight, which is similar to that of the tetrapods, but in
osteichthyeans it is, according to Thorson (1961), about half as large. However, as
the number of species of bony fishes is vast and the measurements have been
made on comparatively few, it remains to be seen whether such a difference is a
general characteristic of these animals.
The solute content of the plasma in representatives of the main groups of fishes
has been measured (Table 7.1). The bony fishes that live in the sea generally have
higher solute levels than those of fish in fresh water. Euryhaline fish, like the floun-
der, salmon and eel, have a plasma osmolarity that is about 20% greater in the sea
than in fresh water, and this is the result of an elevated sodium chloride con-
centration. Such marine fish are considerably hyposmotic, two- to threefold less,
to the sea-water that bathes them. The only exception among the Osteichthyes
appears to be the relict crossopterygian Latimeria (arguably a group that once
also may have lived in fresh water) whose plasma is hyperosmotic to sea-water,
due mainly to a retention of urea. It is interesting that the closest living phyletic
relatives of this fish are the lungfishes, and one of these, Protopterus, can also tol-

188
Table 7.1. Osmotic constituents in the plasma of various fishes

Habitat Sodium Potassium Urea Osmolarity

mEqJ-' mEql- ' mM mosmolJ-'

Sea-water 470 12 1070

Osteichthyes
Latirneria chalurnnae' SW* 181 355 1181
(Coelacanth)
Protopterus aethiopicusb FW* 99 8 238
(African lungfish)
Carassius auratus' FW 115 3.6 259
(Goldfish)
Opsanus taud sw 160 5.2 392
(Toadfish)
Platichthys flesus' FW 157 5 304
(Flounder) sw 194 5 364
Anguilla anguillar FW 155 2.7 323
(European eel) sw 177 2.8 371
Salrno salaF FW 181 1.9 340
(Atlantic salmon) sw 212 3.2 400

Chondrichthyes
Raja clavatah sw 289 4 444 1050
(Thornback ray)
Squalus acanthias'·i sw 287 5.4 354 1000
(Spiny dogfish)
Chimaera rnontrosa' sw 360 10 265
(Rabbitfish)
Potarnotrygonk FW 146 1.1 308
(Freshwater stingray)

Agnatha
Myxine glutinosa 1 sw 549 11 1152
(Hagfish)
Larnpreta fluviatilism FW 120 3 270
(River lamprey)

* SW = sea-water; FW =fresh water.

References: • Pickford and Grant (1967). b Smith (l930a). ' Maetz (1963). d Lahlou et al.
(l969b). ' Lange and Fugelli {1965). r Sharratt et al. (l964a). g Parry (1961). h Murray and Potts
(1961). 1 Filnge and Fugelli (1962). i Burger (1965). k Gerst and Thorson {1977). 1 Bellamy and
Chester Jones (1961). m Robertson (1954).

erate large amounts of urea in its body fluids. The marine chondrichthyean fishes,
like the relict crossopterygian Latimeria, which lives in sea-water, also maintain
their body fluids slightly hyperosmotic to sea-water by retaining urea as well as
some sodium chloride (Smith 1936). Chondrichthyeans that live in fresh water,
like the stingray, Potamotrygon, have a much lower plasma concentration due to
a reduction in the levels of both urea and sodium (Table 7.1). The agnathans
exhibit both types of osmotic constitution, the lampreys are hyposmotic to sea-

189
water, while the hagfishes are slightly hyperosmotic. The latter group, however,
does not retain urea for this purpose, but has high salt concentrations in its extra-
cellular fluids.
We can predict the osmotic stresses on the various fishes from the osmotic
concentrations in their body fluids. In fresh water, all fishes tend to gain water by
osmosis while at the same time they may be expected to lose solutes by diffusion.
In the sea, chondrichthyeans, Latimeria and the hagfishes, all gain water by
osmosis, and (except for the latter) may be expected to accumulate sodium
by diffusion. The marine bony fishes and lampreys, which are hyposmotic to
sea-water, lose water osmotically and gain sodium. Measurements of water and
solute balance in the different groups of fishes indicate that such osmotic changes
are occurring, but they differ widely and are adequately compensated for by
physiological adjustments.

1 The Piscine Endocrines

The vertebrate endocrine glands and their secreted hormones make their
phyletic debut in the fishes (see Chap. 2). They possess hormones similar to those
present in tetrapod vertebrates. Notable differences in the fishes are the absence
of parathyroid glands but the presence of what appear to be two additional con-
tributors to the endocrine armoury: the corpuscles of Stannius and the uroph-
ysis. The secreted hormones in the fishes have structures that are homologous to
those in other vertebrates. However, growth hormone and prolactin have not been
identified in the pituitaries of hagfishes and lampreys (superclass Agnatha), but
a novel pituitary hormone, somatolactin, is present in many bony fish. The precise
chemical structures of their hormones, especially peptides, polypeptides and
proteins, often display considerable differences from those in other species of fish
and the tetrapods. These differences appear to reflect the evolution of the hor-
mones among the vast number of piscine species during the long periods of time
that have elapsed since their primaeval origin. The receptors for such hormones
in fish display many differences in their interactions with homologous hormones
from other species. Such differences apparently reflect an evolution of their chem-
ical structures that parallels that of the hormones. Although the piscine hormones
and their receptors may make contributions to osmoregulation similar to those
in other vertebrates, there are also some remarkable differences. Information
about the particular roles of hormones in the osmoregulation of fishes is often
meagre, and generalizations are often not possible. The fishes are a very diverse
group of vertebrates containing vast numbers of species. They can be difficult to
obtain and maintain under experimental conditions. They are also often highly
prone to stress in the laboratory. However, observations on the actions and phys-
iological roles of hormones in fish can provide important insights into the evo-
lution of osmoregulation in vertebrates.

190
1.1 Neurohypophysial Hormones

The neurohypophysis of fish lacks the distinct neural lobe that is present in ter-
restrial vertebrates. However, it contains homologous peptide hormones, though
usually they are stored in smaller quantities. As in non-mammalian tetrapods,
vasotocin is present in all the main phyletic groups extending from the Agnatha
to the Chondrichthyes and Osteichthyes (Fig. 2.5). In lampreys and hagfish,
vasotocin appears to be the only such hormone present, suggesting that it is the
primaeval hormone in this family of peptides. Chemically related peptides have
been identified in invertebrates, including molluscs (Van Kesteren et al. 1992a,b).
The Agnatha may have acquired this gene from such an ancestor. The biosynthetic
precursor of vasotocin, provasotocin, in lampreys is more similar to that in other
vertebrates than to the prohormone in hagfish (Suzuki et al. 1995). This observa-
tion supports the suggestion that the lampreys are part of the main phyletic line
of vertebrates. Most other fish possess at least two different, but homologous, such
peptide hormones (Acher 1996). Lungfish (Dipnoi) have vasotocin and, like many
tetrapods, also mesotocin. However, most other bony fish possess a novel such
peptide, which differs from mesotocin by the presence of a serine residue, instead
of glutamine, at position 4 in the molecule (Heller et al.1961). It is called isotocin.
A plethora of such "neutral" oxytocin-like peptides have been identified in the
cartilaginous fish. As described in earlier chapters of this book, vasotocin con-
tributes to osmoregulation in non-mammalian tetrapods by an ability to exert
an antidiuretic effect. The evidence for such an effect is equivocal in fishes, but it
could have other roles. It has been suggested that the considerable diversity of
neurohypophysial peptides in cartilaginous fish may reflect the lack of a vital
specific effect in these fish (Acher et al.1999). However,Acher has made the inter-
esting suggestion that they could be contributing to the regulation of urea levels
in such ureosmotic fish.

1.2 Adrenocorticosteroids

Adrenocortical tissues have been identified in all the phyletic groups of the
fishes (Henderson 1997). These tissues usually lie adjacent to the kidneys and may
be present on their ventral surfaces. In teleost and agnathan fish, presumptive
adrenocortical tissue may also be situated along the posterior cardinal veins. In
these fish it can be intermixed with chromaffin tissue that secretes adrenaline and
noradrenaline. In lungfish, aldosterone is a major secretion of adrenocortical
tissue. It also produces cortisol and corticosterone in these fish (Idler et al. 1972;
Joss et al. 1994). This mixture of corticosteroids is similar to that seen in amphib-
ians. It is possible that small amounts of aldosterone are produced in some teleost
fish. However, the principal such steroid in the plasma of the Teleostei, Holostei
and Chondrostei is cortisol. Corticosterone is also usually present, and sometimes
small amounts of cortisone. While the primary physiological role of cortisol
is that of a glucocorticoid in most vertebrates, this hormone also makes an
important contribution to the salt metabolism in fishes. Sharks and rays

191
(Elasmobranchii) secrete a novel corticosteroid, !a.-hydroxycorticosterone, from
their interrenal glands (Table 2.3; Idler and Truscott 1972). This steroid has not
been found in any other group of vertebrates. It is not even present in other
cartilaginous fish, such as the Holocephali (chimaeroids). The latter fish secrete
cortisol. Corticosterone and cortisol have been identified in the plasma of a
hagfish,Myxine glutinosa (Phillips et al.l962b; Idler and Truscott 1972). However,
adrenocorticosteroids could not be identified in another agnathan fish, the
lamprey Lampetra jluviatilis (Buus and Larsen 1975). The synthesis of adreno-
corticosteroid hormones in fishes can be increased by ACTH and angiotensin II
(Henderson 1997). Urotensin I, which has structural similarities to mammalian
corticotropin-releasing hormone, also promotes cortisol synthesis in teleosts
(Arnold-Reed and Balment 1989, 1994). In tetrapods, the natriuretic peptides
usually inhibit the synthesis of corticosteroids but in flounder a stimulation has
been observed (Arnold-Reed and Balment 1994).

1.3 The Renin-Angiotensin System

A distinct renin-secreting juxtaglomerular apparatus, such as that in mammals,

has not been identified in the kidneys of most fish. However, a comparable struc-
ture has been observed in elasmobranchs (Lacy and Reale 1990). Granulated
cells, like those containing renin in other species, have been found in many bony
fish, where they are associated with the afferent glomerular arteriole. They include
the Teleostei, Dipnoi, Chondrostei and Holostei (Nishimura 1978, 1987). In 1942,
Friedman and his associates found renin activity to be present in the kidneys
of freshwater but not in marine teleosts. However, it has subsequently also been
identified in marine species, though its concentrations are lower than in the
freshwater fish (Chester Jones et al. 1966; Sokabe et al. 1966; Capelli et al. 1970).
Teleost renin can interact with the plasma substrate angiotensinogen from all
non-mammalian tetrapods, to produce angiotensin (Nolly and Fasciola 1973).
Elasmobranch renin can even interact with mammalian angiotensinogen
(Henderson et al. 1981). Renin activity has also been found in the corpuscles of
Stannius, which abut the kidney, in eels (Chester Jones et al. 1966). The chemical
structures of angiotensins in fish usually differ in a characteristic way from those
of tetrapods (Fig. 2.6). "Fish angiotensin" typically contains asparagine, instead
of aspartic acid, at position 1 in the molecule. An interesting exception is
the bowfin (Holostei), which has the "tetrapod-type" peptide (Takei et al. 1998).
Elasmobranch angiotensin is unique as it contains proline, instead of valine,
at position 3. This amino acid substitution could be influencing its tertiary
structure and activity (Takei et al. 1993). The Agnatha appear to lack the
renin-angiotensin system.

192
1.4 Natriuretic Peptides

The fishes possess at least four different types of natriuretic peptides. Two of
these are homologous to tetrapod ANP and CNP (Fig. 2.9). However, they lack a
homologue to BNP. A different type of natriuretic peptide has been found in the
ventricular heart muscle of teleosts and is called ventricular natriuretic peptide
(VNP) (Takei et al. 1994a, b, c). A fourth distinct type of such peptide has been
identified in salmon, Salmo salar (Tervonen et al. 1998). It is formed only in the
heart, and its structure suggests that it could be an ancestor of ANP and BNP. This
cardiac peptide (CP) contains 29 amino acids residues and has been identified in
the plasma of 9 genera and 15 species of teleosts (Tervonen 2000). CNP has been
identified in the heart and brain of several elasmobranchs (Schofield et al. 1991;
Suzuki et al. 1992). It is, apparently, the sole such natriuretic peptide present in
these fish, and it has been suggested that it also may be a primordial form of these
hormones. Immunohistochemical observations indicate that natriuretic peptides
are present in the heart and brain of hagfish (Reinecke 1989; Donald et al. 1992).
However, at this time, their precise chemical nature does not appear to have been
described.

1.5 Catecholamines

The hormones adrenaline and noradrenaline are described chemically as cate-

cholamines (Fig. 2.8). Both may be present in the plasma of fish, where they also
function as neurotransmitters in sympathetic-adrenergic neurons (Randall and
Perry 1992). They are secreted by chromaffin tissue. Some of the catecholamines
in the plasma may originate as an overflow from adrenergic nerves. The chro-
maffin tissue in fish may be dispersed, as observed along the posterior cardinal
veins in the "head" kidney of teleosts. In elasmobranchs, this tissue forms paired
clusters along the surface of the kidneys. Chromaffin tissue is present in the heart
of agnathans. In bony fishes, chromaffin tissue often intermingles with adreno-
cortical tissue. In elasmobranchs, noradrenaline quantitatively predominates over
adrenaline, while in teleosts the latter tends to be more plentiful. The secretion of
these hormones occurs in response to such stimuli as hypoxia, hypercapnia,
metabolic acidosis, intense exercise and severe stress. Release may be mediated
by autonomic preganglionic sympathetic nerves, which secrete acetylcholine. It
may also occur in response to direct stimulation of the endocrine tissue. Circu-
lating concentrations of these hormones vary in different species of fish (Reid and
Perry 1994) and at different times of the day and year (Le Bras 1984). There are
several types and subtypes of adrenergic receptors (Chap. 2). For instance, a- and
P-adrenergic receptors, a 1-, az-, P1 - and so on.

193
1.6 Thyroid Hormone

Thyroxine (T4 ) and triiodothyronine (T3 ) are secreted by the thyroid gland (Fig.
2.8). This tissue has been identified in members of all the main phyletic groups
of fishes, including hagfish. Homologous tissues and thyroid hormone-like activ-
ity have even been identified in protochordates, such as the lancelet (amphioxus).
Calorigenic effects of thyroid hormone do not appear to be manifested in fish.
However, they may contribute to the ability of some fish to adapt to solutions of
differing osmotic concentration (see Fontaine 1956). They also can exhibit mor-
phogenetic actions, such as may be involved in the proliferation of salt-secreting
chloride cells (Subash Peter et al. 2000).

1.7 Urotensins I and II

Urotensins I and II (Fig. 2.10) are peptides that were first identified in spinal cord
neurons in teleosts. However, they have since been found in most of the other
groups of bony fish and elasmobranchs but not hagfish or, apparently, lungfish
(Onstott and Elde 1986). In teleosts, these neurons aggregate in the caudal region
to form the urophysis. This tissue has a neurohaemal junction with the caudal
veins, which lead to the kidney and urinary bladder. The possibility that the
urophysis may be involved in osmoregulation is largely based on observations of
changes in its structure following transfers between fresh water and sea-water
(see Larson and Bern 1987). Changes in the concentrations of the biologically
active peptides stored in the urophysis have also been observed in such circum-
stances. Urotensin I, like its homologue, corticotropin-releasing hormone, has
been observed to promote secretion, in vitro, of ACTH from the pituitary of a
teleost, the white sucker, Catastomus commersoni (Fryer et al. 1983). It has also
been shown (in vitro) to directly stimulate the secretion of cortisol from adreno-
cortical tissue in trout (Arnold-Reed and Balment 1994). Urotensin II can stimu-
late Na+ transport across the isolated intestine and urinary bladder of the marine
goby, Gillichthys mirabilis (Loretz and Bern 1981; Loretz et al. 1985). It has also
been found to stimulate Cl- transport across the opercular skin of this fish
(Marshall and Bern 1981). Both urotensin I and II are vasoactive, which has
contributed to the suggestion that the latter may be involved in cardiovascular
regulation in fish (Conlon et al. 1996; Platzack et al. 1998). Such responses could
influence osmoregulation. A homologous radioimmunoassay for urotensin II has
recently been developed (Winter et al. 1999). It was found that in flounder the
plasma concentrations of this peptide were generally higher when the fish were
adapted to sea-water than to fresh water. When flounder adapted to sea-water are
transferred to fresh water there is an transitory decline, for at least 72 h, in its
concentrations in the plasma (Winter et al. 2000). This technique is an important
advance, as it may provide a basis for establishing a role for this putative hormone
in piscine osmoregulation.

194
1.8 The Growth Hormone/Prolactin Family

The adenohypophysis of fishes can secrete growth hormone and prolactin,

which are structurally homologous to these hormones in tetrapods. They have
not been directly identified in the Agnatha, though immunocytochemical obser-
vations suggest that they may be present in lampreys (Wright 1984). Prolactin and
growth hormone can contribute to the adaptation of some euryhaline teleosts to
their transition between life in fresh water and the sea. The chemical structures
of the hormones exhibit marked differences in their amino acid sequences to
those in other vertebrates. Thus, salmon growth hormone and prolactin have a
homology of only about 35o/o to the hormones that are present in humans.
However, in lungfish, the homology to the human hormones is about 60o/o.
Prolactins in teleost and holostean (the bowfin) fish contain only two disul-
phide bridges, compared to three in the tetrapods. However, prolactin in lungfish
(Dipnoi) and sturgeon (Chondrostei) have three such bonds (Noso et al.1993a,b).
The Teleostei appear to have followed a separate line of evolution with respect to
the structure of prolactin. They have also utilized this hormone in their osmoreg-
ulation (see later). Whether these two events are related is unknown. The teleost
Oreochromis niloticus (tilapia) possesses two different prolactins, which have a
homology in their amino acid sequences, of only 69o/o (Specker et al. 1993). Little
is known about prolactin in elasmobranchs. Its presence was originally identified
by its biological activity. Like other vertebrate prolactins, it can promote a "water
drive" response in newts (see Chap. 6).
Most of the actions of growth hormone in vertebrates are mediated by insulin-
like growth factor-! (IGF-1). This polypeptide (see Chap. 2) is induced, mainly in
the liver, by growth hormone. Several IGF-Is have been identified in teleosts (Chen
et al. 1994; Duan 1997). Their structures are highly conserved and remarkably
similar to those in other vertebrates. Although IGF-1 has not been identified in
the plasma of agnathans, an IGF-1 gene has been found in hagfish (Nagamatsu
et al. 1991).
Somatolactin is a novel member of the growth hormone/prolactin family
which was first identified in the pituitary glands of flounder (Ono et al. 1990). It
is formed in the pars intermedia and has since been identified in many other bony
fish (Rand-Weaver et al. 1992; Do res et al. 1996; Amemiya et al. 1999 ). It is released
into the circulation in response to a variety of potentially stressful stimuli such
as external acid conditions, low environmental calcium levels and changes in
osmotic concentrations of the bathing media (Rand-Weaver et al. 1993; Kakizawa
et al. 1993, 1996). Its physiological function is unknown.
Many fish can adapt to life in either fresh water or the sea. Migrations, such as
are often associated with breeding, involve the movement of the fish from the sea
into rivers and back into the sea again. Salmon, trout and lampreys breed in fresh
water, where their young undergo initial growth and development before return-
ing to the sea. Others, like eels, breed in the ocean but subsequently spend a large
part of their life in fresh water. Some species, like the rainbow trout, Oncorhynchus
mykiss, and the marine lamprey, Petromyzon marinus, have landlocked popula-
tions that have discarded such migratory habits, and undergo their entire life cycle
in fresh water. Certain other species like the flounder, killifish and toadfish occupy

195
coastal waters near the mouths of rivers and streams, where they experience vari-
ations in the salinity of the water in which they live. There is not only a variety
of euryhaline fishes, but they exhibit diverse morphological development and
physiological conditions associated with different stages of their life period. These
include the juvenile freshwater salmonid parr and premigatory smolt, and silver
eels, as well as the adult fishes in various stages of their breeding cycle. Many such
fish cannot withstand direct transfers from fresh water to sea-water during all
stages of their development, or even at any season of the year. When such a migra-
tion is made, several days are required to adjust completely to the new osmotic
conditions.
Conte, Wagner and their collaborators (Conte and Wagner 1965; Conte et al.
1966) made some interesting observations of the migratory behaviour, and ability
to adapt to sea-water, of steelhead trout and coho salmon. Populations of these
fish breed and undergo their initial development in the rivers of the northwest of
the United States. When very young juveniles of these salmonids are placed in
sea-water they die, but subsequently, as they grow larger, they can adapt to such
solutions. It is well known that this often occurs at about the time when they
metamorphose from a parr to a smolt, and this also corresponds to their seaward
migration. It was found that it is not necessarily this metamorphosis per se that
results in their ability to adapt to sea-water, but their size also contributes. When
they attain a length of about 15 em, they can adapt to sea-water and indeed in the
juvenile parr coho salmon studied, this was usually seen 6 or 7 months before they
metamorphosed into smolts. This suggests that surface area relative to the body
weight may be important, and that physiological and morphological features may
develop that are associated with the general growth rate, rather than any sudden
metamorphic transformation. Hoar (1951) found that the chloride-secreting cells
in the gills of Pacific salmon underwent a period of rapid development before
migration. This is consistent with the observations of Conte and Lin (1967), who
found an increased rate of branchial cell renewal during salt water adaptation in
young salmonids.
When fish are transferred from fresh water to sea-water, or from sea- to fresh
water, a number of changes take place in the osmotic composition of their body
fluids. Initially, the changes are usually more pronounced than are subsequently
maintained. This period of equilibration lasts for about 48 h in eels and flounder
(Keys 1933; Lahlou 1967) transferred from fresh water to sea-water, but may be
as long as 170 h in the steelhead trout (Houston 1959). Some of the changes which
occur in the steelhead trout during this time are shown in Fig. 7.1. Initially,
there is a marked increase in the concentration of chloride in the plasma and the
tissues, while the overall chloride space increases. After the rather abrupt initial
increases, these levels start to decline after about 24h, and eventually reach equi-
librium 4 or 5 days later. The salt concentration in the plasma of such sea-water-
adapted fish, however, remains somewhat elevated, compared to fish in fresh
water.

196
 (15)

.;
:2
.2
.c
u
CJ
E
1/)
CJ
0.::

2
en
.._
-"'
~
E
.,-
"t:l
.§ (15)

:;:
u
"'
~
1/)
1/)
;::

Water h in Sea Water

Fig. 7.1. Changes in plasma and muscle chloride concentrations in trout (Oncorhynchus mykiss)
after transfer from fresh water to sea-water. (Houston 1959, by permission of the National
Research Council of Canada)

2 Water Exchanges

The skin and gills of fishes are continuously bathed by the environmental solu-
tions and are avenues for movements of water in or out of the animal. The direc-
tion of any net transfer depends on the direction of the osmotic gradient.
The relative surface areas of the skin and gills vary considerably in different
fishes; in the toadfish, Opsanus tau, the gills have an area ten times larger than

197
that of the skin, while in the mackerel, Scomber scombrus, it is 60 times greater
(see Parry 1966). The toadfish has been shown to have a very low permeability to
water and sodium (Lahlou and Sawyer 1969), and this may partly reflect its rela-
tively small branchial surface.

2.1 The Skin and Gills

The skin of fishes is a thick, complex, poorly vascularized structure, which is

liberally supplied with mucous glands and often covered with scales. It has the
appearance of being a substantial barrier to diffusion, but there are few direct
measurements of its permeability. In 1939, Krogh, after considering the available
evidence, concluded that the gills, rather than the skin, are the principal avenue
for exchanges of water and solutes across the integument of fish. Parry (1966)
agreed with this conclusion. Motais and his colleagues (1969) measured the
movements of tritiated water across the gills of several freshwater and marine
fish (Anguilla, Carassius, Platichthys and Serranus) and found that virtually all
the water that was exchanged occurred across the gills. However, the permeabil-
ity of the gills of these teleosts was still found to be low compared to other epithe-
lia, such as amphibian skin and urinary bladder. The permeability coefficient for
water of the gills of rainbow trout, in sea-water, is at least 30 times less than
that of the toad urinary bladder (Isaia 1984). Water movements across the gills
of teleosts have been found to be much less when they are bathed by sea-water
instead of fresh water. The change in permeability occurs very rapidly following
transfer to sea-water. It has been suggested that it could be a direct effect on the
epithelial cells covering the gills (Motais et al.l969; Isaia 1984), such as occurs
when the urinary bladders of toads are bathed (in vitro) with hyperosmotic solu-
tions (Bentley 1961, 1965). The gills of fish are well vascularized. The magnitude
of the flow and the pathways of distribution of blood in the gills can be regulated
by adrenaline and noradrenaline originating both from sympathetic nerves and
endocrine chromaffin tissue (Nilsson 1984). Changes in the distribution of blood
within the gills can result in the recruitment of additional respiratory lamellae.
It is possible that other vasoactive hormones, such as angiotensin II, natriuretic
peptides and vasotocin, could be contributing to changes in the distribution of
blood. The vascular actions of adrenaline on the gills appear to be insufficient to
account for the observed changes in permeability to water. A more direct effect
of this catecholamine on the cell membranes of the gill epithelial cells appears to
be occurring. Such a response results in an increased permeability to water (Pic
et al. 1974; Isaia 1979). Other hormones, such as prolactin, may also contribute to
changes in the permeability of the gills to water.
Information about the permeability of the skin and gills of cartilaginous and
agnathan fish is sparse compared to bony fish. The skin of dogfish, Scyliorhinus
canicula, is about three-times more permeable to water than that of the mud-
puppy, Necturus maculosus, which is an aquatic amphibian (Payan and Maetz
1970). However, it is less permeable than that of the leopard frog Rana pipiens.
The gills of dogfish have a similar permeability to water as those of rainbow trout.

198
Cartilaginous fish, in contrast to marine teleosts, maintain their body fluids
at concentrations that are nearly isosmotic to sea-water. Thus, limiting the
permeability of the gills to water would not appear to be of paramount physio-
logical importance in such fish. Marine myxinoid agnathans also maintain their
body fluids at near-isosmotic concentrations with sea-water. The integument
of Pacific hagfish has been found to be very permeable to water (McFarland
and Munz 1965). However, as the osmotic gradient between the body fluids and
sea-water is low, little net transfer of water occurs. Hagfish appear to gain water
across their integument that is equivalent to less than 0.5% of their body weight
each day (Morris 1965). Agnathan fish living in fresh water accumulate greater
amounts of water across their integument. The migratory river lamprey, Lampe-
tra fluviatilis, takes up water at about the same rate as goldfish. It is equivalent to
about 33% of their body weight each day (Bentley and Follett 1963). Measure-
ments of osmotic water movement across the skin, in vitro, of the river lamprey
(osmotic gradient 210mosmoll~ 1 ) indicate that it occurs at the rate of about
2.5111 em~2 h ~I (Bentley 1962a). This value is similar to the estimate, in vivo, of the
rate of water uptake that occurs across the entire integument, i.e. skin and gills
(Wikgren 1953). The relative osmotic permeability, in fresh water, of the entire
integuments of eels: river lampreys: frogs have been estimated to be 1 : 20: 60
(Wiikgren 1953).

2.2 The Gut

Fishes living in fresh water drink little water, but teleosts in the sea must swallow
sea-water in order to compensate for their osmotic losses (Smith 1930b). Indeed,
if marine teleost fish are prevented from drinking, they rapidly die from dehy-
dration. The rate of drinking appears to relate directly to the fish's needs, for, as
the concentration of the external media increases, so does the amount that the
fish drinks; eels in sea-water drink 325111 (100 gt1 h~\ but if they are placed in a
solution twice as concentrated as the sea, they drink 800111 (100 gt 1 h~ 1 (Maetz
and Skadhauge 1968). The quantity of sea-water swallowed by marine teleosts
each day varies from volumes equivalent to So/o of the body weight in the floun-
der to 12% in the sea-water perch (Table 7.2). These quantities are presumably
largely dictated by the osmotic water loss of the fishes, a factor influenced by their
surface area, as well as the precise properties of the skin and gills. There are few
determinations of drinking rates in non-teleost fishes; the lamprey drinks when
placed in 50% sea-water and myxinoids have been observed to drink, but this
water does not appear to be absorbed (McFarland and Munz 1965; Morris 1965).
Marine chondrichthyeans do not usually appear to drink (Smith 1931).
Drinking by fish principally depends on their osmotic circumstances. However,
some water may be imbibed during feeding and, as observed in amphibians,
be induced by stressful conditions. Hirano (1974) observed that euryhaline
Japanese eels, Anguilla japonica, adapted to fresh water, started drinking imme-
diately when they were transferred to sea-water. They then ceased drinking as
soon as they were returned to fresh water. Haemorrhage resulted in drinking in

199
Table 7.2. Rates of drinking of various fish in fresh water (FW) and sea-water (SW)

ml (100gt1 body
weight day- 1

Osteichthyes
Carassius auratus FW 2 Lahlou et al. (1969a)
(Goldfish)
Tilapia mossambica FW 6 Potts et al. (1967)
sw 27
Anguilla anguilla FW 3 Maetz and Skadhauge (1968)
(European eel) sw 8
Anguilla japonica FW Not detectable Oide and Utida (1968)
(Japanese eel) sw 8
Platichthys flesus sw 5 Motais et al. (1969)
(Flounder)
Salmo gairdneri sw 8 Oide and Utida (1968)
(Trout)
Serranus scriba sw 12 Motais and Maetz (1965)
(Sea-water perch)
Chondrichthyes sw nil. Smith (1931)
Agnatha
Lampetra fluviati/is SW (SOo/o) 15 Morris (1960)
(River lamprey)
Myxine glutinosa sw 6.s• Morris (1965)
(Hagfish)

• Drinking was irregular; most fish did not drink. There was no evidence of absorption from
the gut.

the freshwater eels. As observed in many tetrapod vertebrates, the injection of

angiotensin I or II can induce drinking in many fish. However, this response is
not seen in all fish. The differences have been related to the usual osmotic con-
ditions in the environments that the particular fish occupies (Kobayashi et al.
1983; Kobayashi and Takei 1997). Fish that are habitually stenohaline and live
exclusively in either fresh water or sea-water generally do not respond to admin-
istered angiotensin. The drinking response of fish to this hormone has been
viewed as an emergency one which is not present in species that live in a pre-
dictable osmotic environment. However, there are exceptions, and some teleosts
that have been described as "more or less" stenohaline have been found to respond
to angiotensin. Such fish may be exposed to changes in external osmotic concen-
trations, such as may occur near the mouth of rivers or when they become trapped
in tidal pools. Euryhaline species, such as eels, killifish and flounder, all respond
to the injection of angiotensin by drinking. Two agnathans, the freshwater Arctic
lamprey and the hagfish, Eptatretus burgei, which is marine, and two species of
elasmobranchs were found to be unresponsive. Somewhat unexpectedly, it has
been found that in another elasmobranch, the dogfish Scyliorhinus canicula,
angiotensin II induces drinking (Hazon et al. 1989). Acute decreases in the
blood pressure of these dogfish also resulted in drinking, apparently reflecting
an activation of the renin-angiotensin system. The latter response has also
been observed in European eels (Tierney et al.1995). The drinking responses to

200
reduction in blood pressure can be inhibited by the drug captopril, which blocks
ACE and the conversion of angiotensin I to II. The infusion of atrial natriuretic
peptide to Japanese eels has been observed to inhibit drinking (Tsuchida and
Takei 1998). The response, which did not result in changes in blood pressure, was
accompanied by a decrease in the plasma levels of angiotensin. It is possible that
the ANP may modulate the drinking response, especially during the early adap-
tation of such euryhaline fish to sea-water.
About 75% of the sea-water that is imbibed by teleost fishes is absorbed into
the body fluids. The intestine absorbs water, but as this is a consequence of the
absorption of sodium, a large amount of salt is also absorbed. Most of the diva-
lent ions appear to be retained in the gut, though some are absorbed and later
excreted by the kidney. The bulk of the salt is sodium chloride, which is excreted
through the gills (Keys 1931) leaving osmotically free water in the body. The
amounts of sodium (and chloride) absorbed across the gut of fishes kept in sea-
water amounts to 100 ~Eq (100 gt 1 h- 1 in the flounder, Platichthys flesus (Maetz
1969), 280 ~Eq (100 gt 1 h- 1 in the sea perch, Serranus scriba (Motais and Maetz
1965) and 170 ~Eq (lOOgt 1 h- 1 in the eel, Anguilla anguilla (Maetz and Skadhauge
1968). This is equivalent in a day to 100 to 200% of the total sodium present in
the fish.
Water absorption from imbibed sea-water takes place from the anterior and
posterior intestine of marine teleosts. The fluid that enters the intestine
approaches isosmoticity with the plasma. Water absorption then occurs as a result
of a favourable concentration gradient that is established by the absorption of
sodium chloride (Loretz 1995). It was once considered likely that the dilution
of imbibed sea-water occurred solely in the stomach as a result of the movement
of body water by osmosis and secretion (Smith 1930b ). This water was assumed
to be subsequently reabsorbed in the intestine. This recycling process would be
expected to occur at a metabolic cost. Such a dilution of sea-water has been
observed in vitro in the stomach of eels (Sharratt et al.1964b). There was a simul-
taneous movement of Na+ from the stomach to the plasma. However, the process
of dilution of such sea-water has since been shown to commence in the oesoph-
agus (Hirano and Mayer-Gostan 1976). The oesophagus of freshwater eels has a
very low osmotic permeability to water but in the sea-water-adapted fish, sodium
chloride and water readily cross the mucosa into the plasma. The absorption
of sodium chloride from the oesophagus involves its diffusion down a concen-
tration gradient. There is, in addition, a linked Na-Cl cotransport (Hirano and
Mayer-Gostan 1976; Kirsch and Meister 1982; Parmalee and Renfro 1983;
Nagashina and An do 1994). The precise nature of this salt transport has not been
defined. However, the process can be partly inhibited by the sodium channel-
blocking drug amiloride and also ouabain, which inhibits Na-K-ATPase.
This oesophageal desalination process has been observed in several teleosts,
including flounder, plaice and cod (Loretz 1995). When freshwater-adapted eels
were treated over a period of 7 days with cortisol, the permeability of the oesoph-
agus to Na+ increased (Hirano 1980). When sea-water-adapted eels were treated
with prolactin, the permeability to Na+ decreased. Such responses would be
physiologically apt for such fish adapting to, respectively, a life in sea-water or
fresh water.

201
 The absorption of water from the intestine of eels is dependent on the active
absorption of Na+ (Skadhauge and Maetz 1967; Skadhauge 1969). This process in
teleost fish depends on the activity ofNa-K-ATPase (Smith 1964, 1967; Oide 1967).
This enzyme mediates the extrusion of Na+ across the basolateral surfaces of the
intestinal mucosal cells. Its activity increases in fish adapted to sea-water. If the
adenohypophysis is removed, from eels and killifish, this increase in enzyme
activity fails to occur. However, it can be restored by the administration of ACTH
(Hirano 1967; Hirano and Utida 1968; Pickford et al. 1970b). The absorption of
Na+ from the intestine of teleosts commences with its entry into the mucosal cells,
across their apical plasma membranes (Loretz 1995}. The latter process involves
the activity of at least two cotransport proteins that mediate a coupled ion trans-
port of Na+-K+-2cl- and Na+-cl-. The Na+ is extruded across the basolateral
surface by the Na-K-ATPase, and the Cl- by a cl-/HC0 3- exchange mechanism and
a linked K+-cl- co transport. Atrial natriuretic peptide has been shown to inhibit
the Na+-K+-2cr- cotransport across the intestine of winter flounder (O'Grady et
al. 1985). It has also been shown to inhibit such salt transport across the intestine
of sea-water-adapted eels (Ando et al. 1992} and the goby Gillichthys mirabilis
(Loretz 1996}. Thus, at least three different hormones, angiotensin II, cortisol and
ANP, may contribute to the process by which teleost fish regulate salt, and ulti-
mately water, absorption from the gut.

2.3 The Kidney

The urine produced by the kidneys of fish living in fresh water is the primary
route for the excretion of the excesses of water that are gained across the integu-
ment. In sea-water the kidneys are an important avenue for excretion of divalent
ions that are gained as a result of drinking.
The kidneys of fish (Dantzler 1989) are mesonephric, though non-functional
remnants of the pronephros are sometimes still present. A venous renal portal
system, which supplies the tubules, is usually present. There is an arterial blood
supply to the glomeruli. The nephrons of different species of fish have quite
diverse structures. In freshwater and euryhaline teleost fish, the glomeruli are
usually quite large and numerous, but in marine stenohaline teleosts they are
reduced in size and number. About 30 species of teleosts are aglomerular, includ-
ing a few freshwater species, where the condition is apparently secondary to a
marine ancestry. The renal tubules have multiple separate segments. Freshwater
teleosts have a distinct distal segment that is almost impermeable to water but it
is an important site for the reabsorption of Na+. This segment is not present in
marine stenohaline teleosts. The proximal renal tubules may be subdivided into
segments, usually two. The second segment can be the site of a tubular secretion
of a solution of sodium chloride, which may equal the volume of the glomerular
filtrate. In aglomerular species it is the primary site of formation of the renal
tubular fluid. The proximal tubules are separated from the distal ones by a short
intermediate segment. These tubules lead into the collecting duct system and the
archinephric duct. Over 90% of the sodium chloride and as little as 25% of the

202
water in the tubular fluid is reabsorbed in the tubular-collecting duct system. The
kidney structures of marine elasmobranchs and hagfish (Agnatha) have special
features, which will be described later.
Teleost fish living in fresh water form a copious dilute urine containing low con-
centrations of sodium chloride (Table 7.3). In sea-water the volume is much less
and the concentration approaches isosmoticitywith the plasma. A reabsorption of
sodium chloride still occurs from the renal tubules of marine teleosts, the excess
salt being excreted by the chloride cells in the gills. Tubular secretory processes are
also important for the excretion of divalent ions in marine teleosts. The initial
determinant of the urine volume, except in aglomerular fish, is the glomerular fil-
tration rate (GFR). The basal filtration is dictated by the blood pressure and the
opposing osmotic pressure of the plasma proteins. Changes in urine volume
mainly reflect the GFR. In lampreys (Agnatha) the rate of filtration across individ-
ual glomeruli can be adjusted (Brown and Rankin 1999). However, in teleosts,
increases and decreases in the GFR are due to changes in the numbers of function-
ing glomeruli. This mechanism is described as glomerular recruitment or
glomerular intermittency. Non-filtering glomeruli may still be perfused with
blood, but the pressure is insufficient for filtration to occur. Such changes in the
GFR appear to be due to constriction or dilatation of the afferent and efferent
glomerular arterioles. However, local shunting of blood to different regions of the
kidneys could still be occurring. There are several hormones that are vasoactive
and could be contributing to changes in glomerular activity. They include vaso-
tocin, catecholamines, angiotensin II, natriuretic peptides and possibly urotensins.
Adrenergic nerve stimulation may also be contributing to changes in GFR. These
possibilities will be discussed later. None of them has established physiological
roles in this process in fish. However, most of them have been shown, when admin-
istered pharmacologically, to be able to induce changes in GFR.
There is little evidence to indicate that the reabsorption and secretion of water
and solutes in the renal tubules of fish are directly influenced by their hormones.
It has been suggested that in fresh water prolactin may decrease the permeabil-
ity of the renal tubule to water (Nishimura and Imai 1982). It is possible that renal
tubular permeability and transport processes may respond directly to the local
concentrations of water and solutes. Such concentrations could be influenced by
the rates of delivery of fluid to the tubular mechanisms and reflect the GFR
(glomerular-tubular balance).
Neurohypophysial hormones, especially vasotocin, when administered to fish,
can change the GFR (Sawyer et al. 1982; Pang et al.1983). In high doses, such pep-
tides invariably produce a diuresis (Maetz et al. 1964; Chester Jones et al. 1969;
Sawyer et al. 1976; Logan et al. 1980; Uchiyama and Murakami 1994). The fish
include goldfish, eels, lungfish and lampreys. The response appears to reflect an
increased blood pressure and glomerular recruitment. However, in lower doses,
vasotocin may result in an antidiuresis, due to a decrease of the GFR (Babiker and
Rankin 1973, 1978; Henderson and Wales 1974; Amer and Brown 1995). It is gen-
erally accepted that vasotocin lacks any action on the permeability of the fish
renal tubule to water. However, indirect observations on the ability of vasotocin
to induce the formation of cAMP in nephrons of rainbow trout suggest that it has
some action at this site (Perrott et al. 1993).

203
 Table 7.3. Composition of the urine of fishes

N
0 vol. GFR Tubular Sodium Total Osmolarity
*"" (mlkg- ' h -') H 20% cone. (!J.Eqkg-'h- 1) (mosmoll- 1)
reabsorption (mEql- 1)

Osteichthyes
Protopterus aethiopicus' FW 4.9 14 69 5.5 27 17
(African lungfish)
Amia calvab FW 5.3 8.3 36 9.6 51 31
(Bowfin)
Carassius auratus' FW 13.7 20.4 33 11.5 158 36
(Goldfish)
Esox luciusd FW 0.6 3.1 77 <0.5 z0.5 37
(Pike)
Opsanus tau' sw 0.18 aglom. - 73 13 356
(Toadfish)
Platichthys flesus 1 FW 1.8 4.2 57 30 43 90
(Flounder) sw 0.6 2.4 75 60 36 275
Anguilla anguillag FW 3.5 4.7 25 19 56
(Eel) sw 0.6 1 40 6.5 4
Salmo gairdnerih,;,; FW 4.0 6.5 38 9.3 37
(Trout) sw 0.03 0.4 93 220 (Cl)
Chondrichthyes
Squalus acanthiask,I sw 0.18 3.0 94 339 61 780
(Spiny dogfish)
Pristis microdonm FW 10.4 19 45 "Traces, 54
(Freshwater sawfish)
Agnatha
Lampetra fluviatilisn FW 13.7 21 34 15 106
(River lamprey)
Myxine glutinosa• sw 0.22 - - 480 72 1000
(Atlantic hagfish)

FW = fresh water; SW = sea-water.

' Sawyer (1966). b Butler and Youson (1988).' Maetz (1963). d Hickman (1965).' Lahlou eta!. (1969b). 1 Lahlou (1967). g Sharratt eta!. (1964a). h Holmes
and McBean (1963).; Fromm (1963).; R.M. Holmes in W.N. Holmes and McBean (1963). k see B. Schmidt-Nielsen (1964). 1 Burger and Hess (1960).
m Smith (1936). n Bentley and Follett (1963). o Morris (1965).
 The acute transfer of fish from fresh to brackish water has often been found
to result in a depletion of the storage of vasotocin in the neurohypophysis. This
effect has been observed in many species, including flounder, rainbow trout,
medaka and Japanese lampreys (Haruta et al. 1991; Hyodo and Hirano 1991;
Perrott et al. 1991; Uchiyama et al. 1994). Such observations suggest that changes
in the release and I or synthesis of vasotocin are occurring. However, until the
development of a specific radioimmunoassay for vasotocin became available, it
was not possible to measure the concentrations of this peptide in the plasma. Such
an assay was introduced in 1994 (Warne et al. 1994). The concentrations of vaso-
tocin the plasma of eels, flounder and trout were found to be between 10-12 and
2 x 10- 11 M, which is a little lower than those usually observed in tetrapods. No
consistent differences were observed in the concentrations of this peptide in the
plasma in such fish following adaptation to fresh or sea-water. However, the infu-
sion of hyperosmotic sodium chloride solutions into sea-water-adapted flounder
resulted in a 60% increase in the concentration of vasotocin in the plasma
(Warne and Balment 1995). No change in the concentration of the hormone was
observed following haemorrhage. Atransient increase in the release of vasotocin
was also observed in rainbow trout transferred from fresh to brackish water
(Kulczykowska 1997). It is possible that vasotocin contributes to the initial
adjustment of the GFR and urine flow in some fish, following sudden exposure
to hyperosmotic conditions. However, vasotocin may have other functions in
fish.
The transfer of euryhaline teleosts from fresh to sea-water usually results in a
decline in blood pressure. In European eels there is then a rise in the concentration
of renin in the plasma (Henderson et al. 1976). Such a response would appear also
to initiate a rise in angiotensin II. The administration of large doses of angiotensin
II to American eels results in an increase in blood pressure (Nishimura and Sawyer
1976). In fresh water there is an associated rise in GFR and urine volume. However,
in rainbow trout maintained under experimental conditions where normal blood
pressure was maintained, angiotensin II was found to induce an antidiuretic effect.
This response reflects a decrease in the number of filtering glomeruli (Brown
et al.1980; Gray and Brown 1985; Kenyon et al.1985). Such an effect of the renin-
angiotensin system could be contributing to the decreased urine flow that occurs
when euryhaline teleosts enter sea-water.
Administered natriuretic peptides can influence the urine flow in fish. Such
effects may reflect their vascular action, changes in the GFR and an increased
excretion of sodium (natriuresis). The latter effect could be a primary effect of
such hormones and will be discussed later. Natriuretic peptides can induce an
increase in blood pressure and a diuresis in freshwater and sea-water-adapted
rainbow trout (Duff and Olson 1986; Olson and Duff 1992). This effect appears to
be an indirect one due to the activation of a-adrenergic neural mechanisms. A
diuretic and natriuretic response has been observed in marine aglomerular toad-
fish (Lee and Malvin 1987). Eel atrial natriuretic peptide induces an antidiuresis
in Japanese eels adapted to sea-water but not fresh water (Takei and Kaiya 1998).
The natriuretic peptides have multiple interrelated actions and their possible con-
tributions to changes in the urine flow of fish are not clear. Their concentrations
are usually higher in the plasma of fish adapted to sea-water than those in fresh

205
water (Westenfelder et al. 1988; Evans et al. 1989; Freeman and Bernard 1990;
Smith et al. 1991}. The effects of natriuretic peptides on the kidney would appear
to be more apt in a marine than freshwater environment.

3 Salt Exchanges
Fishes may gain salts from, or lose them into, the fluids that bathe them. The
principal exchanges involve sodium and chloride and, to a much lesser extent,
potassium.
On simple physico-chemical grounds, a net loss of sodium and chloride would
be expected to occur across the integument of fishes into fresh water, while a gain
of these ions may be expected to take place from sea-water. In addition, accumu-
lation of salts occurs as a result of drinking and feeding. Earlier experiments,
especially those of Krogh (1939}, indicated that such movements of sodium chlo-
ride do indeed take place, but the technical methods then available did not allow
a prompt assessment of the relative magnitude of the various exchanges to be
made. The subsequent ready availability of radioisotopes considerably facilitated
such measurements. In 1950 Mullins used 24 Na to measure the total rate of salt
exchange in sticklebacks, Gasterosteus aculeatus. The isotopes were placed in the
external bathing fluids (alternatively, they can be injected into the fish}, and the
amounts accumulated by the fish were measured at intervals. If the fish are in salt
balance, the total influx and efflux of the ion will be similar and can be taken to
indicate the total rate of its turnover by the fish. This has been called the rate
constant (K) for the ion and is often expressed as the percentage of the total
(exchangeable) amount of that ion in the body that moves in (KJ or out (K 0 ) of
the fish each hour. This provides a relatively simple and accurate method for
comparing the permeability of different fish to salt in various circumstances.
Sticklebacks in sea-water were found to exchange 20% of their total exchangeable
sodium each hour, while in fresh water only about 1% was moved. Potassium
was exchanged far less rapidly; in sea-water only 0.4 mEq kg- 1 h- 1 was transferred
(compared to 11 mEqkg- 1 h- 1 for sodium}, but this increased about three-fold in
fresh water.
When the rate constants for sodium were measured in other fishes in sea-water
they were found to vary greatly, though the movement of this ion in fresh water
is always small (Table 7.4}. In sea-water, Tilapia mossambica exchange 66% of
their total sodium each hour, but in the toadfish, Opsanus tau, only 16% is moved
in this time. Marine chondrichthyeans and hagfish exchange sodium far less
rapidly than teleosts: less than 1% each hour.
Differences in the total ion exchange of different fish are due to several factors,
probably the most prominent being their relative surface areas. Nevertheless,
other factors also can result in differences in the rates of exchange, and these
include the specific permeability of the gills and skin, the amounts of salt that
may be accumulated through the gut as a result of feeding and drinking, and that
which is unavoidably lost in the urine. As will be seen the latter is usually of minor
importance.

206
Table 7.4. Total sodium fluxes* in fish bathed in various media

Total Na K (%of total Weight/g

flux j.tequiv exchangeable
(lOOgt 1 h- 1 Na h- 1)

Osteichthyes
Carassius auratus'·b FW 27 <1 90-220
(Goldfish) 190mM Na Cl 553 8
Opsanus tau' 10%SW 52 <1 200-700
(Toadfish) sw 805 16
Blennius pholisd 10% sw 50 8 2.5-7
(Blenny) sw 2700 45
Platichthys flesus' FW 43 <1 60-390
(Flounder) sw 2600 45
Anguilla anguillar FW 4 <0.1 60-120
(Eel) sw 1321 33
Fundulus heteroclitus8 ·h FW 60 <0.1 9-20
(Killifish) sw 2020 35
Gasterosteus aculeatus' FW 60 1-2
(Stickleback) sw 1000 20
Tilapia mossambicai FW 200 3 0.5-3
sw 6000 66
Serranus scribak sw 3100 Approx. 60 30-80
(Sea-water perch)
Chondrichthyes
Scyliorhinus caniculus' sw 59 0.5 40-380
(Spotted dogfish)
Squalus acanthiasm sw 90 0.9 4000
(Spiny dogfish)
Hemiscyllium plagiosum" sw 75 0.74 155-1100
(Lip shark)
Agnatha
Myxine glutinosa 0 sw 40 <0.1 Approx. 25-50
(Hagfish)

* Given from measurements of outflux.

• Bourguet et a!. (1964). b Lahlou et al. (l969a). ' Lahlou and Sawyer (1969). d House (1963).
' Motais and Maetz (1965); Motais eta!. (1966). r Maetz eta!. (1967a). 8 Maetz et a!. (l967b).
h Potts and Evans (1967).' Mullins (1950).; Potts et a!. (1967). k Motais and Maetz (1964).
1 Maetz and Lahlou (1966). m Burger and Tosteson (1966)." Chan eta!. (l967b). o Evans and
Hooks (1983).

3.1 The Skin and Gills

As described in the previous section, the skin is generally considered to be rela-

tively impermeable to the movements of solutes, as well as water, the principal
exchanges taking place through the gills. However, in some teleost fish there are
areas of the skin on the head, including the lining of the operculum, that are the
site of cells which can contribute to ion exchanges (Burns and Copeland 1950;
Karnaky and Kintner 1977; Marshall1977}. We must, however, await precise mea-
surements of cutaneous permeability in different species of fish.

207
 Gills in Sea- Water. The flounder, Platichthys Jlesus, in sea-water exchanges
about 2600J.LEq sodium (100gt 1 body weight each hour (Table 7.4}. This repre-
sents 40% of its total exchangeable sodium. About 25% of this sodium is absorbed
through the gut (Motais and Maetz 1965) so that 75% of the total sodium accu-
mulated by these fish takes place through the gills. In the sea perch, Serranus
scriba, 90% of the sodium taken up from the sea-water takes place through the
gills. The extrabranchial gains of sodium, which occur as a result of drinking, are
extruded through the gills, urinary losses making up less than 0.1% of the total.
The gills of such fish in sea-water are thus the site of considerable sodium
exchange, with the efflux exceeding the influx by an amount which is about equiv-
alent to that gained through the gut.
Keys (1931} used a perfused heart-gill preparation of the eel to demonstrate
an active extrusion of chloride by the branchae into the external sea-water.
Isolated gills of eels have also been shown to secrete chloride actively into the
sea-water that bathes them (Bellamy 1961}. Such an extrarenal mechanism for
excretion of sodium chloride provided the channel that Homer Smith concluded
must be present in marine teleost fish in order that they can drink sea-water and
maintain a positive water balance. Such active salt excretion appears to be charac-
teristic of marine teleost fish and probably the lampreys (see Morris 1960}, but has
not been clearly demonstrated in chondrichthyeans. Some of the latter, however,
possess an alternative channel for extrarenal salt excretion, the rectal gland.
Immediately following the original demonstration, by Keys, of chloride secre-
tion by fish gills, a histological search was made for a structural element which
could be involved in this process. Keys and Willmer {1932) found some large and
prominent epithelial cells at the base of the gill leaflets in the eel (Fig. 7.2). As
these were not initially seen in freshwater teleosts or marine chondrichthyeans,
it was concluded that they may be concerned with the extrusion of chloride and
were termed chloride-secreting cells. They are now usually called chloride cells or,
sometimes, ionocytes (see Chap. 1). These cells are rich with mitochondria and
have a complex plasma membrane and intracellular tubular system. Na-K-ATPase
is present on their basolateral borders. This enzyme maintains a low concentra-
tion of Na+ in the cells, thus allowing a linked diffusion of Na+ and cl- to occur
into the cell across its basal surface (Silva et al. 1977}. This process is now known
to be mediated by the Na+-K+-2cl- cotransport protein. The accumulated cl-
diffuses out of the cell, down its electrochemical gradient, across the apical surface
of the chloride cell. The Na+ crosses the gills in the same direction, also following
its electrochemical gradient, but through paracellular pathways (Marshall and
Bryson 1998; Fig 1.2).
Chloride cells have been identified in most fishes, including freshwater teleosts,
lampreys, elasmobranchs and even hagfish. However, their number and morpho-
logical development varies. They appear to have reached the epitomy of their fre-
quency in marine teleosts. In euryhaline fish they may proliferate, differentiate
and hypertrophy prior to their migration into sea-water. Conte and Lin in 1967
made the first such observations on the proliferation and renewal of chloride
cells in the gills of young salmon in sea-water. The enzyme Na-K-ATPase has been
identified in the gills of killifish (Epstein et al. 1967} and Japanese, European and
North American eels (Utida et al. 1966; Jampol and Epstein 1970; Motais 1970}.

208
Fig. 7.2. Diagramatic representation of the gill leaflets of the European eel (Anguilla anguilla)
showing the chloride-secretory cells. a Respiratory epithelium; b blood vessels; c chloride-
secretory cell. (After Keys and Willmer 1932)

The activity of this enzyme increases considerably when these fish are adapted to
sea-water. When euryhaline teleosts are transferred from fresh water to sea-water,
this increase in the levels of Na-K-ATPase in the gills usually occurs over a period
of 3 to 7 days. However, in some species, such as killifish, Fundulus heteroclitus,
there may also be a more rapid response, taking 0.5 to 3h (Towle et al. 1977;
Mancera and McCormick 2000). The increase in the enzyme's activity, as well as
salt extrusion from the gills, can be inhibited in European eels by the adminis-
tration of actinomycin D (Maetz et al. 1969; Motais 1970). The effect was also
observed in the killifish. This drug blocks the formation of mRNA. This mRNA
could be mediating the synthesis of new subunits of Na-K-ATPase or factors
involved in its activation (Mancera and McCormick 2000). The activity of Na-K-
ATPase is four to five times greater in teleosts that live in sea-water as compared
to fresh water (Kamiya and Utida 1969; Jampol and Epstein 1970). Its concentra-
tion in the gills of marine elasmobranchs is about the same as that in freshwater
teleosts.

209
 While chloride cells are clearly involved in the extrusion of Cl- from the gills
of marine teleosts (Foskett and Schaffey 1982), their possible role in the absorp-
tion of salt in fresh water is not clear. In fresh water the branchial chloride cells
of euryhaline teleosts "dedifferentiate" and become reduced in size and possibly
number. Sodium chloride is accumulated across the gills of such fish from very
dilute solutions. However, the quantity of salt is very much less than that which
is extruded by the fish when they are in sea-water. The lower levels of Na-K-
ATPase in the gills of freshwater fish is consistent with this difference in salt trans-
port. In sea-water-adapted teleosts, the Cl- follows its electrochemical gradient
through the chloride channels that are present in the apical plasma membrane of
the chloride cells (Fig. 1.2). In fresh water, Na+ and/or cl- are accumulated across
this membrane. Several processes may be involved in this uptake, including cl-
/HC03- and Na+/H+ or NH/ exchange transport proteins. However, it is currently
considered more likely that the Na+ enters the cell through specific sodium chan-
nels and follows an electrochemical gradient established by a vacuolar (V)-type
H+-ATPase. This enzyme extrudes protons across the apical plasma membrane
(Fig. 1.2). Conclusive evidence that Na+ and Cl- uptake across the gills of fresh-
water teleosts involves chloride cells is lacking. Pavement epithelial cells, which
predominate on the lamellar and interlamellar surfaces of the gills, could also be
involved.
Several hormones have been observed to influence the movements of salt
across the gills of fish.

Cortisol. In 1967, Ian Chester Jones and his collaborators removed the adreno-
cortical tissue from European eels (Chan et al. 1967a; Henderson and Chester
Jones 1967; Mayer et al.1967). (This surgical operation does not appear to be pos-
sible in other teleosts.) In the sea-water-adapted eels, an excessive accumulation
of Na+followed but the administration of cortisol restored normal concentrations
of this ion. In freshwater eels, the Na+ levels became depleted, but could also be
restored by the injection of cortisol. This adrenocorticosteroid thus appeared to
be contributing to the salt balance of the eels in both fresh water and sea-water.
Hypophysectomy results in a loss of salt by many teleosts living in fresh water.
This absence of the pituitary glands results in the lack of several hormones that
can contribute to osmoregulation. In freshwater eels there is a loss of Na+, which
can be reduced by the administration of ACTH (Chan et al. 1968). This effect
appears to reflect the ability of this hormone to promote the secretion of
cortisol. Hypophysectomy in euryhaline killifish reduces the activity of Na-
K-ATPase in the gills (Epstein et al. 1967). This deficiency can be corrected by the
administration of cortisol (Pickford et al. 1970b).
It has been observed that when North American eels are transferred from fresh
water to sea-water there is a rise in plasma cortisol concentration (Fig. 7.3)
(Forrest et al. 1973a,b ). Over a period of several days there is also a closely related
increase in branchial Na-K-ATPase. The administration of cortisol to freshwater
eels has been shown to increase the levels of Na-K-ATPase in the gills (Epstein et
al; 1971; Kamiya 1972). This enzyme was found to be present in the chloride cells.
Cortisol has also been shown to increase Na-K-ATPase activity in branchial chlo-
ride cells in tilapia in fresh water (Dang et al. 2000). In brown trout, cortisol

210
 1200
;:....

.
... 01
z8 800
:::.

=-~
.a >
w 400

~ ~ =
12 ,
260 ! \Plasma cortisol ;6
~i
~ > ~:--·~ 8 8 n
=l
220 ,:::·;...--
_j ~ .----·--<:::;_,___ 3 0
.::a
ii: E 180 .7/ Plasma Na• •.---- \. / • ~''-· 4
'" ~
r • ''~.
~·~~~--~~~_L_i_ _L_L_~-L--N'-~o
140 '1, zh 2 3 4 5 6 7 8 9
Fresh Sea-water
water Days In sea-water adapted

Fig. 7.3. A diagram showing the effects of adaptation of North American eels (Anguilla rostrata)
to sea-water following transfer from fresh water. Upper section Changes in the concentrations
of Na-K-ATPase in the gills and the efflux of Na•; lower section changes in plasma concentra-
tion of cortisol and the plasma Na• concentration. (After Forrest et al. 1973a,b)

increases the concentrations of mRNA for the a-subunit of Na-K activated ATPase
(Madsen et al. 1995).
Cortisol receptors have been identified in the gills of North American eels
(Sandor et al. 1984) as well as in brook trout, steelhead trout and rainbow trout
(Chakkraborti et al. 1987; McLeese et al. 1994; Shrimpton and McCormick 1999).
They have been localized in the chloride cells of chum salmon fry (Uchida et al.
1998).
Cortisol has been observed to increase the numbers and differentiation of
branchial chloride cells (Thompson and Sargent 1977; Dang et al. 2000). It has
been suggested that the primary effect of cortisol in sea-water is to promote the
proliferation and differentiation of chloride cells (Foskett et al. 1983; Foskett
1987).
In fresh water, cortisol appears to be necessary to maintain the integrity of the
branchial sodium chloride transport system. In Japanese eels in fresh water the
administration of cortisol has been found to stimulate the differentiation and pro-
liferation of two freshwater types of chloride cells (Wong and Chan 2001). These
changes were associated with increases in Na-K-ATPase activity. Cortisol also
appears to contribute to maintaining levels of the vacuolar H+-ATPase that is
present in the apical plasma membranes of the branchial epithelial cells. The
chronic administration of cortisol has been found to increase the activity of this
enzyme in freshwater- but not sea-water-adapted rainbow trout (Lin and Randall
1993).

Growth Hormone and IGF-1. In 1956, D. C. Smith observed that the adminis-
tration of growth hormone to brown trout enhanced their ability to adapt and
survive when they were transferred from fresh water to sea-water. This important

211
observation was confirmed, much later, in other salmonids (Komourdjian et al.
1976; Clarke et al. 1977; Bolton et al. 1987). The concentrations of growth hormone
in the plasma of young Atlantic and coho salmon have been observed to increase
at about the time of their transformation from the juvenile parr stage to the
subadult premigratory smolt (Prunet et al. 1989; Young et al. 1989). This hormone
is released into the plasma of rainbow trout and coho salmon when they are trans-
ferred from fresh water to sea-water (Sweeting and McKeown 1987; Sakamoto et
al. 1990). The administration of growth hormone to brown trout and Atlantic
salmon has been shown to increase the numbers of chloride cells (Madsen 1990b;
Prunet et al. 1994). There is also an increase in the activity of branchial Na-K-
ATPase. Such effects are not confined to salmonids. In euryhaline tilapia, Ore-
ochromis mossambica, the injection of growth hormone also increases the levels
of this enzyme in the gills (Sakamoto et al. 1997). These effects of growth hormone
in fish are reminiscent of those of cortisol. In brown trout, the administration of
both of these hormones enhanced the salinity tolerance in a manner that may be
synergistic (Madsen 1990b). Growth hormone has been observed to increase the
numbers of cortisol receptors in the gills of juvenile Atlantic salmon (Shrimpton
and McCormick 1998). This effect could be the basis for the interaction of the two
hormones.
Many of the effects of growth hormone in tetrapods are mediated by IGF-I.
This growth factor is present in the plasma of fish. Administration of IGF-I to
rainbow trout improves their adaptation to sea-water (McCormick et al. 1991).
When these fish are adapted to sea-water there is an increased expression of the
IGF-I gene in the gills and kidney but not the liver (Sakamoto and Hirano 1993).
Administered IGF-I can increase Na-K-ATPase in the gills of coho salmon
(Madsen and Bern 1993), Atlantic salmon (McCormick 1996) and brown trout
(Madsen et al. 1995; Seidelin et al. 1999). In the latter study, the effects were found
to be additive to those of cortisol, which suggests that they may have separate
sites of actions.

Prolactin. In 1956, C. E. Burden found that removal of the pituitary gland of

the euryhaline killifish, Fundulus heteroclitus, resulted in their death within 10
days if they were kept in fresh water. However, when they were in sea-water they
survived. Their death in fresh water is accompanied by an excessive loss of salt
from the body. A similar observation has been made in many, though not all,
teleosts in fresh water (Schreibman and Kallman 1969). Pickford and Phillips in
1959 found that the fatal effects of hypophysectomy in killifish, in fresh water,
could be overcome by injecting them with prolactin. No other pituitary hormones
were effective. Ball and Ensor (1965; 1969) demonstrated that in mollys, Poecilia
latipinna, the loss of Na+ which followed hypophysectomy was prevented by
administered prolactin. Sticklebacks, Gasterosteus aculeatus, normally migrate
from the sea into rivers in the spring (Lam and Hoar 1967; Lam and Leatherland
1969). If these fish are taken from the sea in winter and placed in fresh water, they
die. However, if they are first injected with prolactin, they survive. This hormone
is normally released from the pituitary gland during the spring migration. The
effect of prolactin is due to an inhibition of salt loss from the gills in fresh water
(Maetz et al. 1967a,b; Ensor and Ball1972; Lam 1972). The precise mechanism of

212
this effect is still unknown, but it appears to involve a decrease (dedifferentiation)
in the size, but not the number, of chloride cells in gills and cutaneous epithelium
(Foskett et al. 1983; Herndon et al. 1991). Prolactin is present in the plasma in
higher concentrations in teleosts in fresh water than in salt water (Young et al.
1989; Auperin et al. 1994a; Yada et al. 1994). Receptors for this hormone have also
been identified in the gills (Auperin et al. 1994b). In tilapia in sea-water the
branchial extrusion of Na+ is reduced by 75% following the injection of prolactin
(Dharmamba et al. 1973; Dharmamba and Maetz 1976). This effect suggested that
an inhibition of the activity of Na-K-ATPase could be occurring. Prolactin has
been shown to have such an effect on this enzyme not only in tilapia but also kil-
lifish and mullet (Pickford et al. 1970a; Gallis et al. 1979; Sakamoto et al. 1997).
Prolactin has also been shown to inhibit the effect of IGF-I on the induction of
mRNA for the a-subunit of Na-K-ATPase (Seidelin and Madsen 1999). It is also
possible that prolactin reduces the diffusion permeability of the gills to Na+, but
the nature of such a process is unknown.

Natriuretic Peptides. In tetrapods, the primary nature of the effects of the

natriuretic peptides are to compensate for the expansion of the volume of the
extracellular fluids. Such adjustments involve cardiovascular changes and salt
excretion by the kidneys. Indeed, as described earlier, it has been suggested that
the primaeval role of these hormones was to limit the expansion of the extracel-
lular fluids in marine fish. As such extant fish principally utilize the gills for salt
excretion, there has been considerable interest regarding possible effects of these
hormones at this site. Receptors for natriuretic peptides have been identified in
both the vasculature and epithelial cells of the gills of teleosts. The receptors in
the branchial blood vessels of toadfish were found to be predominantly of the C-
type, which are not linked to guanylate cyclase (Olson and Duff 1993; Donald et
al. 1994). These receptors are associated with the afferent and efferent gill arter-
ies and the blood vessels of the respiratory lamellae. Receptors for natriuretic pep-
tides have been studied in vitro in preparations of gill epithelial cells from
European eels (Broadhead et al. 1992). These receptors appeared to be linked to
guanylate cyclase and were presumably of the A or B type. It has been suggested
that natriuretic peptides may increase the blood flow in the gills (Evans et al.
1989). Such an effect could influence the exchange of Na+. However, a more direct
effect on the chloride cells could also be occurring. Under in vitro conditions
atrial natriuretic peptide was found to stimulate cl- secretion from chloride cells
in opercular epithelia of killifish (Scheide and Zadunaisky 1988). This natriuretic
peptide has also been shown to stimulate the branchial efflux of Na+ in sea-water-
adapted flounder, plaice and dab (Arnold-Reed et al. 1991).

Catecholamines. Adrenaline and noradrenaline can influence the blood flow

and its distribution, and permeability of fish gills (Nilsson and Sundin 1998). a-
Adrenergic receptors can mediate vascular responses that decrease the blood flow
to the interlamellar regions, which contain most of the chloride cells, and divert
it to the respiratory lamellae. On the other hand, P-adrenergic receptors can
mediate vasodilatatory effects that may facilitate blood flow to the interlamellar
region. Keys and Bateman (1932) in their seminal observations on chloride cells

213
in the gills of eels observed that adrenaline inhibited Cl- secretion. This effect has
been observed in other teleosts (Mayer-Gostan et al. 1987). It could be due to vas-
cular effects, but direct actions also occur. Catecholamines have been observed in
vitro to variously decrease or increase cl- secretion from chloride cells in prepa-
rations of the opercular epithelium of killifish (Marshall and Bern 1980;
Zadunaisky and Degnan 1980). Specific antagonists for the a- and ~-adrenergic
receptor-mediated effects of catecholamines were used to study the nature of the
responses. An inhibition of Ct secretion by catecholamines was found to be
the result of stimulation of a-adrenergic receptors. In contrast, stimulation of ~­
adrenergic receptors resulted in increased cl- secretion. In the isolated perfused
head of trout adapted to fresh water, a-adrenergic stimulation increased the influx
ofNa+ while ~-adrenergic stimulation inhibited it (Perry et al.1984). These effects
were not related to haemodynamic changes in gill perfusion. Intracellular mea-
surements of the Cl- concentration have been made on chloride cells from
the gills of freshwater-adapted brown trout (Morgan and Potts 1995). The ~­
adrenergic drug isoproterenol reduced the concentration of cl-. This observation
is also consistent with a direct action on the cells. The effects of catecholamines
on salt exchanges across the gills are unlikely to be persistent ones. Apart
from their actions on CFTR-like chloride channels, the catecholamines may also
influence the activity of Na-K-ATPase. An inhibitory effect appears to be medi-
ated by an adenylate-cyclase-induced phosphorylation of the enzyme (Tipsmark
and Madsen 2001). The responses are rapid and may occur acutely, such as in
response to stress. It has been suggested that they may mediate the rapid decline
in Ct secretion that occurs when fish move from sea-water to fresh water (Foskett
1987).

Neurohypophysial Hormones. The administration of neurohypophysial pep-

tides, including vasotocin, has been observed to promote the exchange of Na+
across the gills of teleost fish (Bourguet et al. 1964; Motais and Maetz 1964, 1967;
Maetz et al. 1964). Such effects could be reflecting their vasoactive effects and the
redistribution of blood in the gills (Maetz and Rankin 1969; Rankin and Maetz
1971). In contrast to the effects of catecholamines, vasotocin appears to constrict
the arterioles supplying the lamellae so that there is an increased blood flow to
the interlamellar regions, which are rich with chloride cells. Such a vascular
response may occur following the administration of quite low doses of vasotocin
(Bennett and Rankin 1986). Whether it could be a normal physiological response
is unknown. It is also possible that the vasotocin is acting directly on the branchial
epithelial cells. Receptors for vasotocin have been identified in such cells of Euro-
pean eels (Guibbolini et al. 1988). Adaptation of these fish to sea-water resulted
in an increase in the amount of vasotocin binding to these receptors. The increase
was paralleled by changes in the number of chloride cells present. The vasotocin
receptors appeared to be of the V1 type, that stimulate the phospholipase C-
phoshatidylinositol mechanism. In teleost gills, somewhat unexpectedly, it
induces a reduction in the activity of adenylate cyclase (Guibbolini and Lahlou
1987). Specific vasotocin V1 type receptors have been cloned and found to be
present in the gills of several teleosts (Mahlmann et al. 1994). Such receptors are
also associated with the pituitary gland in fishes, where, like the V1 type for vaso-

214
pressin in mammals, they could be mediating a release of ACTH (Pierson et al.
1996).

Thyroid Hormone. The earliest observations on the possible roles of hormones

in piscine osmoregulation were made on the actions of thyroid hormones (see
Fontaine 1956). They were mainly concerned with the process of osmotic adap-
tation of teleosts following their transfer from salt water to fresh water. H. J. Koch
and M. J. Heuts in 1942 (quoted by Fontaine 1956) found that feeding thyroid
hormone preparations to three-spined sticklebacks reduced their ability to adapt
to fresh water. However, as related by M. Fontaine, the results of the administra-
tion of thyroid hormone and antithyroid drugs to other species were quite vari-
able. In some fish, osmotic adaptation was enhanced. Fontaine concluded "as to
the mode of action of the thyroid hormone, it is possible that it includes an effect
on the osmoregulatory cells of the gills, ...". D. C. Smith (1956) also observed that
the injection of thyroxine into brown trout "generally raises the salinity tolerance
of trout, (but) the doses required seem above the physiological level". Such obser-
vations have since often been confirmed in other teleosts, especially salmonids
(see, for instance, Fagerlund et al. 1980; McCormick 1995; Saunders et al. 1985).
The administration of thyroid hormone to freshwater tilapia has been observed
to increase the Na+ and cr concentrations in the plasma and branchial Na-K-
ATPase activity (Subash Peter et al. 2000). However, the results in different species
are quite variable and the relationship to salinity tolerance is considered to be not
proven. The physiological basis for such an effect of thyroid hormone on salinity
tolerance is not clear, but has tended to focus on its possible actions on salt-
extrusion mechanisms in the gills. Thyroid hormone receptors have been identi-
fied in the gills of many teleost fishes (Bres and Eales 1988; Lebel and Leloup 1989;
Marchand et al. 2001).
Increases in the concentrations of thyroid hormone in the plasma have been
observed in Atlantic salmon and coho salmon during their transformation from
parr to smolts, which migrate to the sea (Prunet et al. 1989; Young et al. 1989).
Smoltification has also been related to increases in the concentrations of cortisol
and growth hormone in the plasma and a proliferation and differentiation of
branchial chloride cells. Thyroid hormone replacement in hypophysectomized
coho salmon resulted in an inhibition of gill Na-K-ATPase activity (Bjornsson
et al. 1987). A possible synergistic effect between thyroxine and cortisol on the
activity of branchial Na-K-ATPase has been investigated in rainbow trout
(Madsen 1990a). However, the thyroxine was found to be without an effect. In con-
trast, in a non-salmonid fish, tilapia, thyroxine "augmented" the action of corti-
sol in increasing branchial Na-K-ATPase (Dange 1986). A synergistic relationship
between thyroxine and growth hormone has been observed in the sea-water
adaptation and smoltification of amago salmon (Miwa and Inui 1985).
Fish can undergo various types of developmental metamorphoses and in some,
including flounder, thyroid hormone is involved in the transformation (Miwa et
al. 1988; Inui et al. 1994). In summer flounder, Paralichthys dentatus, this process
is accompanied by the development of branchial chloride cells (Schreiber and
Specker 1999). There is also an increase in salinity tolerance and Na-K-ATPase in
the gills. These changes could be inhibited by an antithyroid drug, thiourea, and

215
enhanced by thyroxine (Schreiber and Specker 2000). Unfortunately, at this time,
there seems to be no consensus regarding the physiological significance and role
of the thyroid in osmoregulation. However, there are a number of observations
suggesting that thyroid hormone could be contributing to this process, especially
during metamorphic changes.
A diagrammatic summary of the possible roles of hormones in regulating
salt movements across choride cells in the gills of teleost fishes is shown in
Fig. 7.4.

Cortisol, growth hormone, IGF-I

~
Chloride cell proliferation

l
and differentiation

Prolactin
Apical plasma inhibits? Basal plasma
membrane membrane
External
medium CHORIDE CELL

Cotransporter
(regulation?) +--f--+ 2CI-
.,__ _,I""'--- IK+

Phosphatidylinositol pathway?

Induced by cortisol
and(?) growth hormone Na-K ATPase
Prolactin inhibits? 3Na+ --~~-....
Transgill
potential difference
negative
~4___..:r=::..._---Paracellular route----=l=- Na+

ACCESSORY CELL

Fig. 7.4. A summary of the possible roles of hormones on cr- transport across the gills of teleost
fish. For a more detailed explanation see the text. (Bentley 1998)

216
3.2 The Kidney

The fish kidney (see Dantzler 1989; Braun and Dantzler 1997) functions as a
sodium chloride-conserving organ in fresh water fish. The GFR is high in such
fish and most of the salt in the filtrate is reabsorbed by the renal tubule. Marine
teleosts have a surfeit of salt, but most of this is secreted across the gills. The GFR
in these fish is low. Sodium chloride may be secreted into the renal tubules across
the second segment of the proximal tubule. This process is especially important
in the formation of urine by aglomerular teleosts. The filtered Na+ and cr is
mainly reabsorbed in marine teleosts and is subsequently excreted across the
gills. The kidneys are the principal avenue for the excretion of divalent ions (Ca2+,
Mg2+, So/- and PO/-) and K+ in these fish.
In sea-water, the flounder and sea perch excrete only about 0.1 o/o of the total
accumulated sodium in their urine (Motais and Maetz 1965). When euryhaline fish
such as the flounder and eel are transferred from fresh water to sea-water, the total
renal sodium excretion changes little; if anything, it may decrease in the latter
medium (Table 7.3). In fresh water, sodium and potassium are lost in the copious
dilute urine that is formed. In goldfish, this daily sodium loss equals about 8% of
the total sodium in the body, an amount similar in magnitude to the total accumu-
lated by the fish (Maetz 1963). Lampreys lose a similar proportion of their sodium
in this manner. The pike,Esox lucius, loses as little as 0.02% of its body sodium each
day (Hickman 1965). These renal losses can be replaced by active branchial uptake
of sodium, but in some feeding fish this may not be necessary. The kidneys of
fish do not appear to respond dramatically to excesses of sodium chloride, but this
situation is unlikely to occur in fresh water. Holmes (1959) observed that sodium
loads were mainly excreted extrarenally in rainbow trout. The urinary losses
of sodium are little affected when sodium chloride solutions are injected into
goldfish; indeed, if these are hypertonic, there is a decreased renal loss (Bourguet
et al. 1964). In lampreys, we (Bentley and Follett 1963) found that only 10% of a
dose of injected sodium chloride was excreted in the urine after 24 h.
Sodium is absorbed from the glomerular filtrate of fish. In the goldfish and
lamprey, 93% of this is reabsorbed (Bentley and Follett 1963; Maetz 1963), while
in the pike 99.95% may pass back into the plasma (Hickman 1965). Potassium is
also reabsorbed from the glomerular filtrate of fish and, as observed in the pike
and the white sucker, Catostomus commersoni, it may also be secreted into the
urine across the wall of renal tubules (Hickman 1965).
Information regarding possible hormonal control of renal salt conservation
and excretion in fish is meagre. The administration of vasotocin, usually in large
amounts, has been observed to result in a natriuresis in several species, includ-
ing goldfish, European eels, African lungfish and river lampreys (Bentley and
Follett 1963; Maetz et al.1964; Sawyer 1966; Chester Jones et al.1969). These effects
appear to reflect the vasoactive properties of this peptide, which produces an
increased GFR. Angiotensin II evokes a similar natriuretic response in North
American eels (Nishimura and Sawyer 1976). These effects are unlikely to be of
physiological significance.
Atrial natriuretic peptide has a natriuretic effect in the toadfish, Opsanus tau,
but as this teleost is aglomerular, the response would appear to involve the renal

217
tubule (Lee and Malvin 1987). However, Evans (1995) was unable to detect ANP
receptors in the renal tubules of a close relative, Opsanus tau, and has suggested
that the response may be a "secondary" one. Receptors for natriuretic peptides
have been identified in the kidneys of fish, but they are usually associated with
the glomeruli (Perrott et al. 1993; Sakaguchi et al. 1996). However, Perrott and his
collaborators also demonstrated that ANP stimulated cGMP formation in isolated
nephrons of rainbow trout. This observation suggests that ANP receptors may also
be present in the renal tubules of these fish.
Adrenocorticosteroids regulate the processes ofNa+ reabsorption and K+ secre-
tion in the renal tubules of tetrapod vertebrates (with the possible exception of
some amphibians). However, despite numerous attempts, a direct effect of such
steroid hormones has not been observed in fish. The renal tubular transport of
ions ultimately depends on the integrity of Na-K-ATPase in the renal tubular cells.
The activity of this enzyme has been observed to change in the kidneys of teleosts
exposed to different salinities. However, the observations have not been consis-
tent, possibly reflecting species variability and the prevailing environmental con-
ditions. In the thick-lipped mullet, Chelon labrosus, renal Na-K-ATPase activity
increases when they are adapted to fresh water (Gallis et al. 1979). On the other
hand, sea-water acclimation has been observed to increase renal mRNA for Na-
K-ATPase in the migrating silver phase of European eels (Cutler et al. 2000). In
killifish, the administration of cortisol results in a rise in the activity of renal Na-
K-ATPase in the hypophysectomized fish maintained in sea-water (Pickford et al.
1970b ). In fresh water, prolactin inhibits branchial Na-K-ATPase in these fish but
stimulates the renal enzyme (Pickford et al. 1970a). The latter effect was inter-
preted as a response, which could, appropriately, be mediating Na+ retention. In
intact brown trout adapted to fresh water, cortisol had no effect on the genetic
expression of Na-K-ATPase (Seidelin et al. 1999). Cortisol also had little effect on
renal Na-K-ATPase in thick-lipped mullet adapted to sea-water (Gallis et al.1979).
However, it decreased the activity of this enzyme in the fish adapted to fresh water.
Due to the variability of such observations, the possible role of cortisol in regu-
lating renal Na-K-ATPase is difficult to assess.
Receptors for angiotensin II have been identified in the renal tubules of teleosts
(Cobb and Brown 1992; Marsigliante et al. 1997). It has been suggested that this
peptide may modulate the activity of Na-K-ATPase in the renal tubules of Euro-
pean eels (Marsigliante et al. 2000). Perfusion of the kidney of the freshwater-
adapted fish with angiotensin II resulted in a 1.8-fold increase in the activity of
this enzyme. In sea-water-adapted eels, where the activity of the Na-K-ATPase was
already high, there was no change. The renin-angiotensin system can thus be con-
sidered as another candidate for the hormonal regulation of Na-K-ATPase activ-
ity in the teleost kidney.

3.3 The Urinary Bladder

The urinary bladder of fishes is derived from the mesonephric ducts, and thus
represents an extension of the renal tubules. It is present in many teleost fish, but

218
it is not as capacious as the tetrapod urinary bladder. (The latter is derived from
the cloaca.) Brahim Lahlou in 1967 observed that the urine stored in the urinary
bladder of flounder had lower concentrations of sodium chloride than that col-
lected directly from the ureters. This difference was observed when the fish were
in both fresh water or sea-water. It was suggested that salt was being reabsorbed
from the urinary bladder. Evidence of a similar reabsorption of salt was also
found in the bladder of toadfish (Lahlou et al. 1969b ). Studies, in vitro, on rainbow
trout confirmed that an active transport of Na+ and Cl- was occurring (Lahlou
and Fossat 1971; Fossat and Lahlou 1979). The transport process involved a partial
coupling of the movements of these two ions. Such in vitro experiments have been
extended to many other species of freshwater and marine teleosts (Marshall1995).
The nature of the Na+-Cl- coupling varies in different species. The urinary blad-
ders of teleosts are also osmotically permeable to water. It is usually less in fish
living in fresh water than in sea-water. The active salt transport results in a further
conservation of urinary Na+ and cl- and appears to be a physiologically useful
saving in fresh water (Curtis and Wood 1991). In sea-water the transported salt
mediates fluid absorption from the urinary bladder. In toadfish it has been esti-
mated that without utilizing the activity of the bladder they would need to drink,
and desalinate, 10o/o more sea-water (Howe and Gutknecht 1978). In euryhaline
teleosts it has been observed that such fluid absorption increases when they are
in sea-water as compared to fresh water (Hirano et al. 1971; Johnson et al. 1974).
Preinjection of marine gobies with cortisol has been found to result in an increase
in Na+ transport across the bladder (subsequently measured in vitro) (Doneen
1976). The reported effects of prolactin on such Na+ transport are conflicting.
Some have found it to increase such ion transport (Johnson et al. 1974; Hirano
1975), while others observed little or no change (Foster 1975; Owens et al. 1977).
Differences between species and environmental and experimental conditions
could be contributing to such variations in the response.

3.4 The Gut

The physiological role and functioning of the gut of marine fishes in relation to
the desalination and absorption of imbibed sea-water has been described earlier
in this chapter. In fresh water the intestine provides an extrabranchial avenue for
the accumulation of salt from food and the little water that they imbibe. In fasting
eels, less than O.So/o of the total sodium that is accumulated by fish kept in fresh
water is absorbed through the gut (Maetz and Skadhauge 1968). However, fish that
are feeding actively will be expected to gain more salt, due to its absorption from
the food. The magnitude of this varies with the nature of the diet. In fresh water
a herbivorous or detrital diet contains less sodium chloride than a carnivorous
one. J0rgensen and Rosenkilde (1956a) calculated that the expected accumulation
of chloride by a goldfish from its normal diet would be less than 25o/o the quan-
tity that is normally absorbed by the gills. Carnivorous freshwater fish, like the
pike, probably gain adequate salt from their diet.

219
4 Nitrogen Metabolism and Osmoregulation

Most teleost fish utilize their voluminous aqueous environment to excrete

ammonia (NH3 and NH/) as the end product of their amino acid catabolism (see
Chap.1; Fig.l.S). They are said to be ammonotelic. The elasmobranchs and coela-
canth convert this ammonia to urea, which is less toxic. They utilize most such
urea as an osmolyte to maintain the concentrations of their body fluids at a
slightly hyperosmotic concentration to the sea-water in which most of them live.
They are said to be ureosmotic. The elasmobranchs, in addition, use urea as a
nitrogenous excretory product so they are also ureotelic. Lungfish are usually
ammonotelic. However, when African lungfish aestivate, in mud cocoons, during
periods of drought, they convert ammonia to urea, which acts as a low-toxicity
osmolyte that is stored in their body fluids until water again becomes plentiful.
Most teleosts form small amounts of urea as a result of nucleotide catabolism via
the formation of purines and uric acid. Uricolysis then results in the urea forma-
tion. About 20 species of teleosts have been found to form larger amounts of urea
from amino acid catabolism. These fish include some amphibious species, the gulf
toadfish (Walsh 1997) and Lake Magadi tilapia (Randall et al. 1989). The latter
are the sole teleosts in this east African lake, which is extremely alkaline (pH 10).
Under these conditions, the loss of NH 3 by diffusion across the gills is inhibited.
These fish are completely ureotelic.
Ammonia may be present in the body fluids of fish as NH3 or NH4+.The former
gas is highly soluble and can be sequestered in lipids. It is highly toxic, though
apparently less so in fishes than in mammals. Ammonium (NH4+) at a physiologi-
cal pH of 7 to 8 is predominant, and it is also the primary form of ammonia that
is produced by cells. It is very water-soluble, but not lipid-soluble, and its toxic-
ity is less than that of NH 3 • Ammonia and NH4+ are mainly excreted across the
gills though some appears in the urine (Wilkie 1997). In fresh water, NH3 is the
principal excretory product but in sea-water substantial amounts of NH/ are
excreted. As it is a cation, NH4+can interact with the transport of other ions. These
include the uptake of Na+ across the apical plasma membrane of branchial cells
which utilize the Na+/H+ cotransporter (NHE). The H+ apparently protonates NH 3
to form NH/ , which can diffuse through paracellular pathways to the external
medium. Such protonation, toform NH4+,may also occur in fresh water as a result
of the activity of H+-ATPase, which is present in the apical plasma membrane of
branchial epithelial cells (Lin and Randall 1993). The NH/ may also be trans-
ported across the basolateral membrane of branchial epithelial cells by substi-
tuting forK+ in Na-K-ATPase and the cotransporter Na+-K+-2ct (Claiborne et al.
1982; Mallery 1983; Wilkie 1997).
In the elasmobranchs, lungfishes and probably the coelacanth, the utilization
of ammonia to synthesize urea takes place in the ornithine-urea cycle. This bio-
chemical mechanism is also present in mammals and the amphibians. Carbamoyl
phosphate, formed by the activity of the mitochondrial enzyme carbamoyl
phosphate synthetase (CPSase), is the primary metabolite to enter the ornithine-
urea cycle. In tetrapods, CPSase utilizes NH 4+ to form carbamoyl phosphate.
The enzyme is called CPSase I. In teleosts, elasmobranchs and the coelacanth
there is a variant of this enzyme called CPSase III. It utilizes NH 3 formed from

220
glutamine (Mommsen and Walsh 1989; Anderson 1995). The glutamine is pro-
duced in the liver as a result of the activity of glutamine synthase. It is interest-
ing that lungfish have CPSase I, like tetrapods. While most adult teleosts do not
produce urea as a major end product of nitrogen catabolism, it appears that this
process may be functioning for a short time in their embryos (Depeche et al. 1979;
Wright and Land 1998). The principal enzymes of the ornithine-urea cycle have
been identified in teleost embryos. The genes for these enzymes, including CPSase
III, appear to have been retained by teleosts. However, they are usually not
expressed.
The excretion of urea in fish occurs principally across the gills, but also in the
urine. These processes can be restricted and controlled by the presence of spe-
cific urea transport proteins. They are important for the conservation of urea in
ureosmotic elasmobranchs (see later). Gulf toadfish, Opsanus beta, are normally
ammonotelic but under conditions of stress, such as crowding and polluted water,
they become ureotelic (Walsh 1997; Wood et al. 1997). Under such conditions, the
cortisol concentration in the plasma increases and appears to contribute to the
activation of glutamine synthetase (Hopkins et al. 1995). This hepatic enzyme is
rate-limiting in the process of ureogenesis. Cortisol could also be contributing to
urea synthesis by promoting the production of catabolic nitrogen as a result of a
stimulation of gluconeogenesis.
Toadfish excrete urea in discrete pulses, each lasting for up to 3 h (Wood et al.
1995). This secretion, which appears to occur across the gills, takes place once or
twice a day. It appears to be initiated by a discrete stimulus (Wood et al.1997; Part
et al. 1999). The urea permeability of the gills increases about 30-fold, but the per-
meability to water is unchanged. The mechanism appears to utilize a specific urea
transport protein, which has been compared to that present in the mammalian
kidney (Wood et al. 1998; Part et al. 1999; Walsh et al. 2000). A similar urea trans-
port protein is involved in the excretion of urea in trout embryos (Pilley and
Wright 2000). The mammalian transport protein contributes to absorption of
urea across the renal tubule and the maintenance of the urea concentration gra-
dient in the renal medulla. Its activity is increased by vasopressin. Vasotocin, as
described earlier, can also increase the permeability of the skin and urinary
bladder of amphibians to urea. The pulse of urea excretion across the toadfish
gills is preceded by a decline in plasma cortisol concentration (Wood et al. 1997).
The administration of vasotocin has been shown to result in large increases in
such urea excretion (Perry et al. 1998). It is possible that the pulsatile excretion
of urea is regulated by several hormones, which could be acting synergistically,
and include cortisol, vasotocin and adrenaline (Part et al. 1999). The effects of the
other neurohypophysial peptide that is present in bony fish, isotocin, does not
appear to have been investigated.

S Osmoregulation and the Endocrines of Sharks and Rays

The osmoregulation of sharks, and skates and rays has excited special interest
since it was observed that, unlike marine teleosts, they maintain their body fluids

221
at a concentration that is similar to that of sea-water (Smith 1936}. They are ure-
osmotic and, as described in the last section, are also ureotelic. This process is
complemented by the retention of other solutes, especially trimethylamine oxide
(TMAO) (Table 1.2}. The latter acts as a protective counteracting solute to antag-
onize possible toxic effects of the urea (see Chap. 1). Other aspects of their
osmoregulation are also quite different to that of bony fishes. Some of the general
information has been summarized in earlier sections of this book. The present
account is mainly a synthesis of this information.
The cartilaginous fish (Chondrichthyes) apparently evolved and diverged from
the main line of vertebrates about 300 million years ago. It was once considered
likely that their ancestors lived in fresh water, but their origins are still con-
troversial. Most species are marine, but a few venture into fresh water and are
considered to be euryhaline. At least one small family, Potamotrygonidae, the
freshwater stingrays, live permanently in fresh water and are apparently steno-
haline. Marine elasmobranchs, unlike teleosts, do not normally drink sea-water
in order to gain osmotically free water (Smith 1931}. However, as they are slightly
hyperosmotic to sea-water, they apparently gain small amounts of water by
osmosis across their integument. As the concentrations of Na+ and Cl- in their
body fluids are less than those in sea-water, they gain these ions by diffusion.
However, the rate of such exchanges is much less than in marine teleosts (Table
7.4). The slower uptake of salt partly reflects the absence of significant drinking
and, as the concentration of sodium chloride in their body fluids is higher than
that in teleosts, a lower gradient for the diffusion of these ions. The permeability
of the gills to salt is also much less than it is in teleosts, though permeability to
water is greater. The gills of elasmobranchs have a very low permeability to urea,
which aids its retention in the body. Water and salts are excreted by the kidneys.
The urine is isosmotic or slightly hyposmotic to the plasma. The concentrations
of Na+ and Cl- that are attainable in the urine are similar to those in the plasma,
so that the kidneys do not appear to provide an osmotically economical avenue
for salt excretion. Little or no urea is lost in the urine. The kidney remains the
principal avenue for water excretion and probably, as in teleosts, divalent ions.
In contrast to marine teleosts, the gills do not appear to be the site of significant
salt excretion. It was once generally believed that the elasmobranch gills lacked
chloride cells. However, these cells are now known to be present, though in small
numbers. The elasmobranchs possess rectal salt glands which secrete a fluid
containing much higher concentrations of sodium chloride than present in the
plasma and even somewhat greater than those in sea-water (Table 7.5}. The rectal
gland provides an avenue for salt excretion. However, surgical removal of this
gland does not seem to compromise the fish's osmotic balance (Burger 1962,
1965}. Possibly other mechanisms for salt excretion exist, such as the gills, which
can assume a salt excretory role in some circumstances.
The control and integration of the unique physiological mechanisms involved
in urea retention and salt excretion in elasmobranchs is of considerable interest.
These fish have a full complement of the vertebrate endocrine glands and the
homologous hormones that they secrete. However, although several such hor-
mones are known to contribute to the osmoregulation in other vertebrates, such
roles have not been established in the elasmobranchs. A plethora of different neu-

222
Table 7.5. Comparison of the composition of the rectal gland secretion of Squalus acanthius
with that of its plasma, urine and sea-water. (Burger and Hess 1960)

Osmolarity Sodium Potassium Chloride

mosmolt' mEql- 1

Sea-water 1000-llOO 470 12 550

Rectal gland secretion 1018 540 7 533
Plasma 1018 289 5 246
Urine 780 339 2 203

rohypophysial peptides, including low concentrations of vasotocin, have been

identified in their neurohypophyses (Acher et al. 1999). Their diversity and evo-
lutionary persistence has been a source of wonder, but their physiological roles
are still unknown. Elasmobranchs possess distinct adrenocortical interrenal
glands which secrete adrenocorticosteroids (Chester Jones and Mosley 1980;
Henderson and Garland 1980). Corticosterone has been identified in the plasma,
but the predominant such steroid is !a-hydroxycorticosterone, which appears to
be unique to these fish. When it is administered to tetrapod vertebrates, the latter
have "mineralocorticoid" activity (Grimm et al. 1969). However, such an effect
has not been conclusively demonstrated in cartilaginous fish. Interrenalectomy in
the skate, Dasyatis sabina, has been observed to result in a decrease in the con-
centration of urea and Na+ in the plasma (DeVlaming et al. 1975). The adenohy-
pophysis contains ACTH, which can stimulate adrenocorticosteroid synthesis
(Hazon and Henderson 1985), prolactin and growth hormone. Hypophysectomy
in dogfish has been observed to reduce the turnover of body water, though this
effect was absent in the little skate (Payan and Maetz 1971; Payan et al. 1973).
A renin-angiotensin system is present and a mammalian-like juxtaglomerular
apparatus has been identified (Hazon et al. 1999). Elasmobranch angiotensin has
a unique structure (Fig. 2.6). Angiotensin II has activities in elasmobranchs
similar to those in other vertebrates. It can promote the secretion of !a-
hydroxycorticosterone (Hazon and Henderson 1985). It may also be contributing
to cardiovascular homeostasis. Although elasmobranchs do not normally drink,
or seem to need to, the administration of angiotensin II }:las been observed, in
some circumstances, to promote drinking in the dogfish, Scyliorhinus canicula
(Hazon et al. 1989). However, this response has not been observed in all elasmo-
branchs (Kobayashi and Takei 1997). The C-type natriuretic peptides (CNP) have
been identified in the heart and brain of elasmobranchs and they are also present
in the blood (Schofield et al. 1991; Evans 1995; Evans et al.1989; Suzuki et al.1994).
The CNP may contribute to cardiovascular homeostasis and, as described below,
appears to regulate secretion by the rectal salt gland. Other osmoregulatory roles
may have evolved for the secretions of endocrine glands in cartilaginous fish, but
it is possible that they may be mediating other types of responses.
Osmoregulation involving the retention of urea, accumulation of water and the
excretion of salts appears to be an integrated process in elasmobranchs involving
the gills, kidneys and rectal salt gland. The liver may also contribute to this process
by changes in urea synthesis.

223
 The Gills. The role and functioning of the gills in the osmoregulation of elas-
mobranch fishes differ considerably from marine teleosts. However, it is consis-
tent with their ureotelic and ureosmotic habitude. The permeability of the gills
to urea is very low, though that to water is high (Part et al. 1998). Mitochondria-
rich cells, which appear to function like chloride cells, are present (Laurent and
Dunel1980). Na-K-ATPase is also present in the gills but at much lower levels of
activity than in marine teleosts (Jampol and Epstein 1970). The exchange rate of
Na+, which mainly occurs across the gills, is much less in elasmobranchs than
marine teleosts, but it is similar to that of freshwater teleosts (Table 7.4). Changes
in blood flow may influence branchial exchanges of solutes and water. Small doses
of noradrenaline have been observed to decrease gill blood flow in the blacktip
reef shark (Chopin and Bennett 1995). This effect appears to be an a-adrenergic
one. Higher doses of noradrenaline elicited a ~-adrenergic response and an
increase in the blood flow. Possible changes in the distribution of blood within
the gills were not studied. Adrenaline has been observed to increase the diffusion
permeability to water in a perfused preparation of dogfish gills (Part et al. 1998).
Receptors for the C-type natriuretic peptide have been identified in the gills of
the Japanese dogfish, Triakis scyllia (Sakaguchi and Takei 1998). Some of these
receptors were linked to guanylate cyclase and the formation of cGMP. As sug-
gested by Evans and his collaborators (Evans et al. 1989), this peptide could be
contributing to the control of branchial blood flow.
The presence of specific cl- and/or Na+uptake or secretion mechanisms in the
elasmobranch gill is uncertain. An active cl- secretion mechanism has been ten-
tatively identified in dogfish gills (Maetz and Lahlou 1966; Bentley et al. 1976).
The observed electrochemical gradient across the gills could not completely
account for a passive efflux of the cl-. A saturable electroneutral Na+influx was
also observed, which was decreased by reduction in external pH. Such processes
appear to involve exchanges with H+ and HC03-and may primarily contribute to
acid-base balance rather than osmoregulation (Evans 1982).An H+-ATPase, which
could be involved in such exchanges, has been identified in the mitochondria-rich
cells in the gills of the spiny dogfish (Wilson et al. 1997).
The low permeability of the gills of elasmobranchs to urea is a major factor in
maintaining their ureosmotic way of life. It has been proposed that the apical
plasma membrane of branchial epithelial cells provides the barrier to such diffu-
sion (Part et al. 1998). The accumulation of urea in these cells appears to be pre-
vented by the activity of a urea-transporter protein, which is associated with the
basolateral plasma membrane of these cells. This transporter passes urea that is
accumulated in the cells back into the blood. Such a urea-transporter protein,
named ShUT, has been identified and cloned in the spiny dogfish (Smith and
Wright 1999). Its amino acid sequence has a 66% identity to a similar protein, UT-
A2, which is present in the rat kidney. The ShUT is expressed in the kidney of the
dogfish, but related proteins, as their mRNAs, were also identified in the gills.
Roger Acher (Acher et al. 1999) has suggested that in elasmobranchs vasotocin,
or related oxytocin-like peptides, could be involved in regulating the activity of
such urea-transport proteins.
Specific binding proteins and receptors for !a-hydroxycorticosterone and
angiotensin II have been identified in the gills of elasmobranchs (Burton and

224
Idler 1986; Tierney et al. 1997}. While such observations suggest that the recep-
tors may mediate physiological activity and influence the functioning of the
gills, the nature of such effects is unknown. Elasmobranch angiotensin II has
been observed to constrict the branchial artery of Japanese dogfish (Hamano et
al. 1998). Thus, it could be contributing to the regulation of branchial blood
flow. By analogy with teleosts, one may suspect that !a-hydroxycorticosterone
could be influencing ion exchanges, but there is no direct evidence for such
an effect.

The Kidneys. Elasmobranchs have kidneys with well-developed glomeruli and,

in contrast to marine teleosts, a nephron that includes a distal tubule segment.
The nephrons are long and contain five distinct segments that are arranged to
form two complete hairpin loops (Boylan 1972; Lacy et al. 1985). This morpho-
logical arrangement appears to be a countercurrent mechanism. It may be con-
tributing to the retention of urea and the ability of the tubular system to actively
reabsorb this metabolite. This process may be utilizing the activity of the ShUT
urea transport protein (Smith and Wright 1999}. Such urea conservation is a
major function of the kidneys in elasmobranchs.
The GFR in marine elasmobranchs is high compared to that of marine teleosts
(Table 7.3}. Urine flow is quite low, due to an efficient reabsorption of more than
90% of the glomerular filtrate. The urine is usually slightly hyposmotic and the
Na+ concentration is similar to that of the plasma. Thus, the kidney cannot effect
significant changes in the plasma Na+ concentration, but it could be mediating
isosmotic adjustments of extracellular fluid volume.
The control of urine formation and its composition probably involves changes
in the GFR and the reabsorption and secretion of fluid and solutes by the renal
tubule. Such processes could involve neural and hormonal regulatory mecha-
nisms. However, there is little direct information about such processes. A possi-
ble action of !a-hydroxycorticosterone on the renal tubule of elasmobranchs is
an attractive extension of the role of such corticosteroids in tetrapod vertebrates.
It has been suggested (Armour et al. 1993}. The administration of mammalian
atrial natriuretic peptide into the spiny dogfish was found to decrease the blood
pressure and the GFR, resulting in an antidiuresis and salt retention (Benyajati
and Yokota 1990). This action contrasts with its natriuretic and diuretic effects in
other vertebrates and may reflect the size of the dose of peptide given. Possible
actions of neurohypophysial peptides on kidney function do not appear to have
been reported in elasmobranchs.

The Rectal Gland. Elasmobranchs, as described in Chapter 1, can excrete con-

centrated solutions of sodium chloride in the secretions of the rectal gland. The
fluid is nearly isosmotic to the plasma and contains almost pure sodium chloride
at a concentration which is similar to that of sea-water (Table 7.5}. It provides a
mechanism for adjusting the sodium chloride concentration and the volume of
the extracellular fluids. The principal stimulus for its secretion is an increase in
the volume of these fluids rather than their concentration (Burger 1962, 1965). In
contrast to the nasal salt glands of birds and reptiles, a direct neural control mech-
anism is not involved. Burger suggested that "volume receptors" may control

225
secretion through the intervention of some "undefined hormone". Over 30 years
later, this hormone has been shown to be the C-type natriuretic peptide (CNP).
In elasmobranchs it is secreted by the heart in response to volume expansion of
the extracellular fluid (Solomon et al. 1992).
The primary ion that is secreted by the rectal gland is cl- with Na+ following
down its electrochemical gradient (see Chap. 1). The process of formation of the
secretion appears to be the same as occurs in branchial chloride cells. High con-
centrations of Na-K-ATPase maintain low intracellular concentrations of Na+ in
the tubular cells of the rectal gland. This gradient allows an inward diffusion,
across the basolateral surface, of the Na+ -K+-2Cl- cotransport protein (Silva et al.
1999a). The accumulated cl- diffuses out of the cell across its apical plasma mem-
brane. This process occurs through specific CFTR-like chloride channels (see
Chap. 1). The precise mechanism of action of CNP is quite complex (Silva et al.
1999b) and involves at least three processes. (Fig. 7.5). The CNP interacts with
guanylate cyclase-linked receptors on the basal side of the secretory cells, result-
ing in the formation of cGMP. The latter alone cannot stimulate secretion but is
aided, synergistically, by a parallel effect of CNP, which results in the activation
of protein kinase C. Earlier studies had shown that vasoactive intestinal peptide
(VIP) could, via activation of adenylate cyclase, stimulate secretion (Greger et al.
1988). However, this action was only observed in vitro (Solomon et al. 1985).
Vasoactive intestinal peptide is associated with nerve cells in a local neural
network in the rectal gland. Its release from these nerves is promoted by CNP.
Thus, at least three interacting mechanisms are involved in the stimulation of
rectal salt gland secretion by CNP.

Expansion
of extracellular
fluid volume ----?8 ...y
Natriuretic peptide
Rectal salt gland

CN;fe~=te; ~nsic
I
Chloride channel
nerves

1
CFTR-iike
pathway in rectal gland

GC-8
receptor

Vasoactive
PhOsphatidyl intestinal
inositol peptide
~-- pathway? ~

VIP receptor ~ PK= protein kinase

Apical PLC= phosphOlipase C

Basolateral
plasma plasma
membrane AC= adenylate cyclase
membrane

Fig. 7.5. Diagrammatic depiction of the processes involved in stimulation of the secretion of
the rectal salt gland of elasmobranch fish by the C-type natriuretic peptide (CNP). The response
appears to involve the combined parallel effects of activation of guanylate cyclase, adenylate
cyclase and, possibly, phospholipase C. For more details see the text. (After Silva eta!. 1999b)

226
 Adaptation of Sharks and Rays to Fresh Water. Most elasmobranchs live
exclusively in the sea, but a few species venture into brackish and even fresh water.
Some apparently make only brief excursions into the mouths of rivers so that
little adaptation is necessary (Price 1967). However, other species stay for longer
periods of time in estuarine conditions and are considered to be euryhaline. The
latter include some skates (genus Raja), which live along the east coast of the USA
(Payan et al. 1973), and the sawfish, Pristis microdon (Smith 1936). The shark Car-
charhinus leucas lives for extended periods in Lake Nicaragua, but, contrary to
earlier impressions, it returns periodically to the sea. Stingrays belonging to the
family Potamotrygonidae live permanently in freshwater rivers, far from the sea.
These elasmobranchs include the Amazon stingray (Potamotrygon spp.). Other
members of this family have been identified in African rivers, but at least some
of these have now been shown to belong to the family Dasyatidae (Thorson and
Watson 1975). The latter family are mainly marine, but a few species live in fresh
water and their fossils have been identified in freshwater sediments.
With their well-developed glomeruli and a distal renal tubular segment for the
reabsorption of Na+, elasmobranchs appear to be well equipped to deal with the
vicissitudes of fresh water. Under such conditions, the GFR and urine volume
increases and the reabsorption of water in the renal tubule declines. Sodium reab-
sorption from the glomerular filtrate increases. The concentrations of urea in the
plasma decline in fresh water but they are usually still maintained at levels of 100
to 200 mM. In skates, this change does not reflect an increase branchial perme-
ability but an increase in the excretion of urea in the urine (Payan et al. 1973).
Whether it is due to a regulated change in renal tubular reabsorption or an
unavoidable consequence of an increased GFR is unknown. Urea synthesis in little
skates (Raja) declines under such conditions (Goldstein and Forster 1971). In
another euryhaline skate, Dasyatis sabina, transfer from sea-water to dilute (33%)
sea-water was found to be associated with the accumulation of a prolactin-like
activity in the pituitary glands (de Vlaming et al. 1975). This observation sug-
gested that prolactin could be acting to reduce the permeability of the gills, as
observed in teleosts. The Amazon stingray, Potamotrygon, lives exclusively in
fresh water. The concentrations of urea in its plasma are even lower (about 1 mM)
than in most mammals (Griffith et al. 1973; Gerst and Thorson 1977; Bittner and
Lang 1980). Attempts to adapt these fish to 50% sea-water did not result in any
significant accumulation of urea. They appear to lack the facility for its accu-
mulation as an osmolyte. The Amazon stingray cannot survive in sea-water and
lacks the renal tubular countercurrent system that apparently contributes to the
conservation of urea by marine elasmobranchs. The rectal gland regresses
and becomes non-functional in elasmobranchs living in fresh water {Oguri 1964).
The Na+ concentration in the plasma of elasmobranchs living in fresh water
declines. This change could reflect unavoidable losses by diffusion across the gills
and more voluminous urine. The manner by which they maintain adequate salts
in their body fluids in such circumstances is unknown. Possibly salt in the diet is
sufficient for their needs. However, teleosts living in fresh water utilize an active
salt-uptake mechanism in their gills, and such a process would also appear to be
appropriate for such elasmobranchs. Possibly the Na/H+ exchange process, which
appears to be primarily dedicated to acid-base balance (see above) is adequate

227
for such salt uptake. Pang and his collaborators (1977) described "preliminary"
experiments on freshwater stingrays in which an influx of Na+was observed. This
process was saturable, suggesting that an active transport was occurring.
The adaptations of such elasmobranch fish to life in fresh water have excited inter-
est and curiosity since Homer Smith drew attention to their plight over 70 years
ago. Almost nothing is known about the possible roles of endocrines in such
adaptations.

6 The Hagfish
Hagfish (class Myxini) are jawless fishes (superclass Agnatha). They are exclu-
sively marine with a worldwide distribution, often living at great depths (see
Hardisty 1979). The two most common genera are Myxine and Eptatretus. Like
sharks and rays, they maintain the concentrations of their body fluids at con-
centrations that are isosmotic or slightly hyperosmotic to sea-water (Table 7.6).
However, in contrast to the cartilaginous fish, the Na+ and cl- concentrations in
their plasma are remarkably similar to those in sea-water. They do not utilize
organic osmolytes to balance the osmotic concentrations of their extracellular
fluids with that of their external bathing solution. This observation indicates that
vertebrate life can exist when the cells are bathed by a concentration of salt similar
to that of sea-water, just as occurs in marine invertebrates. The composition
of their plasma, their lowly phyletic status and their relationship to fossil
ostracoderm ancestors of the vertebrates suggests that they are the closest living
relatives of early vertebrates. The lampreys (class Cephalaspidomorpha) are
also agnathans and many are euryhaline. In sea-water, like teleosts, they maintain
their body fluids at a concentration which is hyposmotic. The Agnatha appear to
be diphyletic with the two classes sharing a common pre-Cambrian ancestor
(Hardisty 1979). The lampreys may be closer to the main line of vertebrate evo-

Table 7.6. Concentration (mMkg- 1 water) of solute in the body fluids of Myxinoidea

Myxine glutinosa Eptatretus stouti

Sea-water• Serum• Muscleb Urine' Mucous secretiond

Sodium 470 549 33 481 95

Potassium 12 11 142 13 207
Chloride 550 563 41 536
Calcium 8 5 2 10 11
Magnesium 50 20 13 28 39
Trimethylamine oxide nil 87
Amino acids 291

The concentrations of sea-water in all these observations was not as in reference a but the dif-
ferences in composition are consistent.
References: • Bellamy and Chester Jones {1961). b Robertson {1976).' Morris {1965). d Munz
and McFarland (1964).

228
lution, but the hagfish appear be more similar in their habitude to primaeval
vertebrates.
It has been said that hagfish have no osmoregulation. Certainly, few osmotic
exchanges are expected to occur between their extracellular fluids and sea-water.
However, some solute gradients do exist, especially for Ca2+ and Mg2+, which
necessitate some regulation of the composition of the extracellular fluids.
The composition of the intracellular fluid differs considerably from that of the
extracellular one. The ratio for the ion concentrations cell water/serum water are
13: 1 forK+ and 0.06: 1 for Na+ (Table 7.6). The pattern of a relatively high intra-
cellular concentration of K+ and a low one of Na+ and Cl-are similar to those in
other animals. Intracellular osmotic balance is achieved by the presence of amino
acids and TMAO. Thus, osmoregulation continues to be essential at the barrier
of the extracellular and intracellular fluid but, due to the high extracellular ion
concentrations, it may require special adaptations in hagfish.
Attempts have been made to perturb the osmotic balance of hagfish by placing
them in hyposmotic and hyperosmotic solutions in order to see if any physio-
logical adjustments may then occur (Munz and McFarland 1964). The fish rapidly
succumb when they are transferred directly from sea-water to 25% sea-water.
(This solution is equivalent to about 0.8% sodium chloride.) However, they can
survive for at least 7 days when transferred directly from sea-water to 80 or 120%
sea-water. When these hagfish were replaced in sea-water, the latter survived, but
those from the dilute sea-water subsequently died. The acute responses were a
shrinkage and loss of body water in the hyperosmotic solution and a swelling in
the hyposmotic one. They appeared to behave like osmometers. The swelling that
occurred in 80% sea-water was followed by a slow return, over several days, to
their original weight. Nevertheless, as described above, these fish succumbed
when replaced in sea-water. In 120% sea-water the hagfish lost 25% of their body
weight and maintained this condition. When they were returned to sea-water they
regained their original weight and survived. Changes in the external osmotic con-
centration have also been shown to result in compensatory increases in the con-
centrations of intracellular amino acids (Cholette et al. 1970). The amino acid
levels in the extracellular fluids remained low. Regulation of the volume of the
extracellular fluids under conditions of external osmotic change may depend on
urinary excretion. Compensation may be "automatic" and result from adjustments
of the GFR due to changes in the concentrations of plasma proteins and, possi-
bly, the blood pressure (McFarland and Munz 1965; Alt et al. 1981).
Most vertebrate hormones appear to exist in hagfish, including those that are
involved in osmoregulation in other vertebrates. Vasotocin was identified in the
pituitaries of Myxine glutinosa by Follett and Heller ( 1964b ). The structure of its
precursor, provasotocin, has a homology in its amino acid sequence of only 47%
with lamprey provasotocin (Suzuki et al. 1995). It was suggested that the hagfish
provasotocin may have a greater homology to the precursor of a homologous
peptide, conopressin, which is present in molluscs. Corticosterone and cortisol
have been identified in the plasma of Myxine glutinosa (Phillips et al. 1962b; Idler
and Truscott 1972). ACTH, which could be controlling such adenocorticosteroid
secretion, appears to be present in the pituitary (Strahan 1959). Catecholamines
have also been identified in hagfish (Randall and Perry 1992). However, the renin-

229
angiotensin system has not been found in the Agnatha. Immunoreactive assays
have observed natriuretic peptides in the plasma of Myxine, though its precise
type is unknown (Evans et al. 1989).lt appears that neither growth hormone nor
prolactin is present in the Agnatha.
The integument (skin and gills) of hagfishes is very permeable to water
(McFarland and Munz 1965; Rudy and Wagner 1970). However, exchanges of Na+
are highly restricted Table 7.4. The skin is liberally supplied with mucous glands,
which can secrete copious amounts of fluid containing K+, Mg2+and Ca 2+in higher
concentrations than those in the plasma (Table 7.6). It has been suggested that
these glands may provide a mechanism for the extrarenal excretion of the ions
(Munz and McFarland 1964). The functional kidneys are mesonephric and have
large, well-developed glomeruli that open directly into the archinephric duct.
Such anephric glomeruli are unique among the vertebrates. Little fluid or sodium
chloride reabsorption appears to occur in the archinephric duct (Munz and
McFarland 1964; Alt et al. 1981). Thus, the kidney does not appear to contribute
to the control of the overall osmotic concentration of the body fluids. However, it
could be regulating the volume. The concentrations of other solutes in the urine
suggest that K+ and Mg2+ are secreted into the archinephric duct and that glucose
is reabsorbed there. The kidney may also contribute to acid-base balance. The
hydrostatic pressure in the glomeruli of Myxine is, at most times, not great enough
to promote ultrafiltration against the opposing osmotic forces of the plasma
proteins (Riegel 1998, 1999). A fluid secretory process may be involved in urine
formation. Adrenaline and noradrenaline enhanced this process, possibly by
increasing the blood flow through capillaries involved in the secretory process.
Whether such an effect of catecholamines could be normally contributing to this
urine formation is unknown. Receptors for natriuretic peptides have been iden-
tified in the kidney of Myxine glutinosa (Kloas et al. 1988; Toop et al. 1995a). They
have been found in the glomeruli as well as the archinephric duct. These recep-
tors are linked to guanylate cyclase, suggesting that they could be functioning just
as in other vertebrates. Such natriuretic hormone receptors could be mediating
changes in renal function that contribute to the regulation of the volume of the
extracellular fluids. This action would be consistent with the previously suggested
primaeval function of these hormones.
The gills of hagfish, despite earlier doubts, contain mitochondria-rich cells
which appear to function like chloride cells (Elger and Hentschell 1983; Bartels
1985). They are the site of carbonic anhydrase activity (Mallatt et al. 1987) and
Na-K-ATPase (Choe et al.1999). The concentrations of the latter enzyme appear
to be relatively low and like those in the gills of elasmobranchs. The chloride cells
may be the site of the Na+/H+ and Cl-/HC03- exchanges which have been observed
to take place across the integument of hagfish (Evans 1984). Such mechanisms
exist in freshwater teleosts, where they contribute to acid-base balance. Natriure-
tic peptide dilates the ventral aorta of Myxine, and this response may lead to
an increase in gill perfusion (Evans 1991). Receptors for this hormone have
been identified in the aorta of this fish as well as in the gills (Toop et al. 1995b).
These receptors in the gills were of two types; guanylate cyclase-linked ones and
"clearance" (C-type) receptors. The latter are present in other vertebrates but their
function is unknown. Natriuretic peptide receptors in the gills, via a vascular or

230
even direct effect, could be mediating salt exchanges across the gills, as observed
in teleosts. However, at this time, such an effect has not been demonstrated in
hagfish. Few attempts appear to have been made, or reported, to study the effects
of the administration of hormone preparations to hagfish. In 1962, Ian Chester
Jones and his colleagues administered aldosterone and deoxycorticosterone, as
well as ACTH, to hagfish that were placed in dilute (60%) sea-water. This strategy
was used in an attempt to elicit conditions where an osmoregulatory response
may be physiologically appropriate. No effects on plasma Na+ were observed, but
its concentration in muscle declined. Whether the effect was due to a decrease in
intracellular Na+ or a decline in the extracellular space of the muscle was not
determined. The primary site of the effect is obscure, but it could be due to a
decrease in plasma volume following increased Na+excretion. However, this is idle
speculation. Currently, many assays are available for detecting receptors for hor-
mones, which, apart from natriuretic peptides, include vasotocin and adrenocor-
ticosteroids. A scan for such hormone receptors in various tissues in hagfish could
be highly illuminating.

231
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284
Index

ACE, see angiotensin-converting enzyme adrenocorticosteroids (corticosteroids) 68,

Acetylcholine, secretion of salt glands 125, 162,191, 229
149 see also adrenal cortex, aldosterone,
- sweat glands 87 cortisol, corticosterone, I a-
ACTH, see adrenocorticotropic hormone hydroxycorticosterone
active transport 11, 13, IS adrenocorticotropic hormone (ACTH,
- chloride 33 corticotropin) 62, 65, 69, 74, 96, 99,
- potassium 15 109, 129, 115, 134, 194,229
-sodium IS -effects 69,98, 168, 180,192,202,210,223
-water 12, 19 adrenomedullin 74
see also sodium-potassium activated aestivation 40, 106, 143
ATPase, chloride cells, colon, gills, - in African lungfish 220
intestine, kidney, rectal gland, - -amphibians 7, 157, 158, 167, 169, 181, 184
salt glands, skin, urinary bladder - - reptiles 143
adenohypophysis 61 -urea accumulation during 40, 157
adenosine 3', 5' monophosphate aggrephores 80
(cyclic AMP) 54 aglomerular kidneys, see kidneys
adenylate cyclase 53, 64, 72, 78, 141,214,226 aldosterone 68
ADH, see vasopressin -distribution in vertebrates 69, 97, 99, Ill,
adrenal cortex 68, 97, 99, lOS, 191 liS, 134, 162
- and salt in diet lOS - effect on colon, in amphibians 93, 180
see also adrenocorticosteroids, - -birds 115, 123, 127, 132
adrenocorticotropin, angiotensin II, - - mammals 93
aldosterone, corticosterone, cortisol, - - reptiles 147
I a-hydroxycorticosterone, - kidney, in amphibians 177
adrenalectomy and interrenalectomy --mammals 104
- in amphibians 177, 180 - - reptiles 146
- - birds 123, 125 - salivary glands 92
- - eutherians (placentals) 92, I 08 - salt glands ISO
- - fishes 210, 223 - skin in amphibians 168, 176
- - marsupials 103 -sweat glands 91
- - monotremes 98 - urinary bladder, in amphibians 178
- - reptiles 146, ISO - - reptiles 147
adrenaline 71, 193 - mechanism of action 81
-action on blood pressure 71 -secretion 104, 105, 111, 147
--gills 198,213,214, 221,224 - - effects of angiotensin II 69
- - kidney 170, 230 - - adrenocorticotropic hormone 69, 180
- - salt glands 125, ISO - - salt-depletion 92, 94, 105, 176, 180, 186
-- skin (amphibian) 166, 167, 176 - - synthesis 50
- - sweat glands 87, 88 see also adrenal cortex
--urinary bladder (amphibian) 179 ammonia (and ammonium, NH/) 39
see also adrenal medullary tissue, - and active sodium transport 40
adrenal medullary tissue - excretion, through gills 220
(chromaffin tissue) 71, 74, 193 - - kidney 140
see also adrenaline, noradrenaline -- skin 181
amphioxus, see protochordates CBG, see corticosteroid-binding globulin
angiotensin II 66, 67, 136, 162 CFTR channels, see chloride channels
-effects in amphibians 185 cell membrane 20
- - birds 115, 129 cGMP, see cyclic guanosine monophosphate
--fishes 192,200,205,217,218,223,225 chickens, see domestic fowl
--mammals 98, 109 chloride, active transport
- - reptiles 136, 151 - in gills 28, 208, 216
- effects on, blood pressure 66 - - intestine 30, 75
- - sodium appetite 29, 66, 96, 109, 129 --kidney 37
- - synthesis of adrenocorticosteroids 69, - - salt glands 33, 226
115 --skin (amphibian) 174
- - thirst 29, 66, 95, 109 see also chloride cells, gills, rectal gland,
see also renin salt glands
angiotensin-converting enzyme (ACE) 66, chloride channels 13, 28, 56,214,226
201 chloride cells 24, 26, 76, 208, 209, 212, 224,
antelope 87, 90, 96 230
aquaporins 14,18,37,38,80,175 -effects of adrenaline 213
atrial natriuretic peptide (ANP), see - - cortisol 211
natriuretic peptides --growth hormone 212
AVP, see vasopressin -- IGF-I 212
AVT, see vasotocin - - natriuretic peptide 213
--thyroid hormone 194,215
- - vasotocin 214
bat 85,106,109,110 - in migration 196
behaviour, and water metabolism 99, 103, - structure 26, 27, 208, 209
104, 106, 118, 136, 138, 160 see also gills, sodium-potassium-activated
betaine 5 ATPase
blood volume 5, 96, 116, 158 chromaffin tissue, see adrenal medullary
body temperature, and evaporative water tissue
losses 24, 97, 99, 102, 106, 113, 118, 137 cloaca 31, 126, 139, 140, 142, 145, 147, 148
see also hyperthermia - interrelationship with nasal salt glands
body size, effects on water exchanges 8, 31, 127
106,113,117,137 --with colon 126, 147
see also evaporation cocoons 7,24,167,220
Brattleboro rats 107 coelacanth 5, 40, 42, 188,220
breeding cycles, and availability of water colon (large intestine) 29, 90, 126, 139, 142
90, 105, 152, 182 - effects of hormones on water and salt
see also reproduction, lactation, milk absorption from 90, 93, 127, 172
Brunn effect, in amphibians, see see also cloaca, rectal caecae
water balance response colour change (skin) 136
budgerygah 116,119,128,130 conopressin 63
see also parrots corticosteroid-binding globulin (CBG) 51
bullfrog 162, 163, 169, 171, 178 corticosteroids, see adrenocorticosteroids
corticosterone 68
- distribution in vertebrates 69, 97, 99, 111,
caecilians 155, 158, 163, 172, 174, 182 115,134,162,191,223,229
calcium 54 - effects, on colon 127
calmodulin 55, 82 --moulting 168
camel 25,87,90,91,95 - - salt glands 150
cAMP, see cyclic adenosine monophosphate - - toad bladder 178
capillaries 22 corticotropin (ACTH), see
carbamoyl phosphate synthetase (CPS) 41, adrenocorticotropic hormone
181,220 cortisol 68
catecholamines, see adrenaline, adrenal -distribution in vertebrates 69, 97, 111,
medullary tissue, noradrenaline, 162,191,229
dopamine - effects, on amphibian skin 162
cattle 29, 87, 88, 89, 93 --gills 210,212,215,221

286
- - kidneys 218 echidna 97
- - oesophagus 201 eels 188, 195, 196, 198, 199,200,201,202,
- - urinary bladder 219 203,205,208,209,210,211,212,213,214,
cotransporters (ion) 16 217,218
counter-current systems, in nasal passages egg-laying, and availability of water 130,
25, 106, 117, 138 152, 182
- in kidneys 35, 120, 225 emu 131, 132
crab-eating frog 3, 7, 157, 159, 166, 169, 171, ENaC (epithelial Na channels) 30, 37, 56,
173, 181, 182, 184 57, 70, 79, 81, 82, 83,127,174,175,184
crocodile 133, 139, 140, 142, 148,151 evaporation 11, 86, 119, 137, 152, 160
cutaneous drinking 24, 176, 185 - from respiratory tract 24, 117, 137
cyclic adenosine monophosphate (cAMP) --skin 118, 137
54,78,226 - - amphibians 167
cyclic guanosine monophosphate (cGMP) --birds 117
56,75,226 - - mammals 99
- - reptiles 137
see also sweat glands
DAG, see diacyl glycerol exchange diffusion 17
dehydration 96, 104, 131, 142, 158, 164, 165 extracellular fluid 5, 129, 229
- evaporative water loss in 88, 102, 118
-lethal limits of 4, 116, 157
-release of hormones in 107, 109, 115, 121, faeces, loss of water and salts 90, 119, 139
122,129,141,166,173 see also cloaca, colon
- sweating in 87 flounder 26,32, 194,195,196, 199,200,201,
see also urine, vasopressin, vasotocin 202,208,215,219
desert lizards 137, 139, 140, 141, 142, 147, flying 113, 119, 121,122, 130
150, 151 food 9
desert rodents 89, 90, 106 -water and salt content 86, 87,94, 105, 110,
see also kangaroo rats 116, 123, 128, 151, 184,219
desert tortoises 133, 143, 145, 151, 152 freshwater rays 189, 222, 227
deserts 4 frogs and toads, see bullfrogs, crab-eating
-and life of amphibians 157, 165 frog, green toad reed frogs, spadefoot
- - birds 130, 131 toad, tree frogs, Xenopus
- - mammals 104, 106
diabetes insipidus 89, 107, 121
see also neurohypophysial hormones, G-proteins 53, 54
neurohypophysectomy gastrointestinal tract, see cloaca, colon,
diacylglycerol (DAG) 54 intestine, rectal caecae
diffusion 9 gerbils 107, 108, 109
- facilitated 10 gills 25,64
see also exchange diffusion, osmosis - blood supply 27, 198,213, 224
dinosaurs 34, 40, 43 - roles in osmoregulation 198
dogfish 18,33,198,200,223,224 --in Agnatha 199,230
dolphins 110, 111 --Amphibia 159, 175
domestic fowl (chicken) 116, 120, 121, 123, --Chondrichthyes (sharks and rays) 27,
124, 126, 127 198,224, 227
dopamine 62, 65,71 - - teleosts 198, 208, 215
drinking 29 - roles in salt metabolism 208
- in amphibians 184 - - effects of hormones on 210
- - birds 120, 128, 129 --water metabolism 198
- - fish 26, 29, 199, 200 - - - effects of hormones on 198
--mammals 86, 95, 102, 104, 110 see also chloride cells, sodium-potassium
- - reptiles 146, 151 activated ATPase
- periodic 104, 128, 151 glomerulus 35, 41 , 120
- of salt solutions 95, 110, 123, 129,151 -filtration rate (GFR) 36, 111, 120, 140, 169,
see also angiotensin II, thirst, thirst centre 217
ducks 123, 124, 125,126 - effects of adrenaline 170, 203

287
-- adrenomedullin 75 -amphibian skin 176
- - angiotensin II 205 insulin-like growth factor I (IGF-I) 53, 65,
- - natriuretic peptides 73, 203, 205, 225 195,211,212
--vasotocin 121, 141, 169, 203 intercellular fluid 5, 96
- intermittent function of 38 interrrenals 68, 192, 223
--birds 120 intestine (small) 30
- - fishes 203 - absorption of sea-water 201
- - reptiles 140, 145 intracellular fluid volume 5, 7, 229
- relative development of in different species ion channels 13, 16
35,168,225 see also chloride channels, ENaC,
see also kidneys potassium channels, sodium channels
glucocorticoids 56, 68 ion exchangers 13, 17
glumitocin 63 ion "pumps" 13, 15
glycerophosphocholine 7 ion cotransporters 13, 16
green toad 7, 159, 177, 181 isotocin 63, 191
growth hormone (somatotropin) 55, 64,
195,211, 212,215,223
guanine 24,41,167 jerboas 107, 109
guanylate cyclase 56, 74, 75, 76, 224, 226, 230 juxtaglomerular apparatus 66, 98, 115, 192
guanylins 75, 93
gular flutter 25, 118
see also temperature regulation kangaroos 88,90,93,95, 96,98,103, 104,105
gulls 33, 121, 124, 125, 129 kangaroo rats 90, I 06, 107, 108, 109
see also sea birds kidney 34
gut 28 - aglomerular 35, 36, 140, 202, 217
see also cloaca, colon, intestine, rectal -function, in amphibians 168, 177
caecae, salivary glands - - birds 120, 123
- - fish 202, 217, 225, 227, 230
--mammals 93, 110
W -ATPase 15,210,211,224 - - reptiles 140, 145
hagfish 35,42, 192,193,194,195,199,200, see also glomerulus, loop of Henle, renal
206, 228 portal system, urine, vasae rectae,
heat, see body temperature, deserts, vasopressin, vasotocin
evaporation, respiration, sweat glands killifish 105,200,208,209,210,212,213,214
hopping mouse 89, 95, 109 kinases,protein 54,55,56,76,79,80, 83,226
horse 87
humans 87,91
hydrins 161 lactation, effect on water and salt balance
hydrogen ions and sodium metabolism 15 86,90,95
!a-hydroxycorticosterone 69, 192, 223, 225 see a lso mammary glands, m ilk,
11~-hydroxysteroid dehydrogenase 81, 127 reproduction
hypernatremia, in amphibians 157 lampreys 42,188,192,195, 199,203,205,
- reptiles 136, 146 217
see also sodium excess lizards, see desert lizards, marine iguana
hyperthermia 25, 96, 106, 118 loop of Henle 35, 89, 99, 120
see also body temperature lungfish 7,40, 69, 162,188,203, 220
hypophysectomy 64 LVP, see lysine-vasopressin
- in amphibians 173, 176, 180 lysine-vasopressin (LVP) 63, 100, 103
--fish 210,212,223
hypothalamus 60
hypoxanthine 24 macula densa 35, 38, 66, 67, 115
mammary glands 64
see also lactation, milk
IGF-!, see insulin-like growth factor-I manatee 110, 111
Inositol-1,4,5-trisphosphate (IP3 ) 54 marine iguana 33, 133, 148
Insulin, and sodium transport across mechanisms ofhormone action 52
amphibian bladder 179 - angiotensin II 54

288
- aldosterone 81 see also glumitocin, isotocin, mesotocin,
- guanylins 76 neurohypophysectomy, oxytocin,
- mineralocorticoids 32 phenypressin, seritocin, vasopressin,
- vasopressin 78 vasotocin
- vasotocin 78 neurohypophysis 61,62
melanocyte-stimulating hormone (MSH) see also neural lobe, neurohypophysial
136 hormones, neurohypophysectomy
mesotocin 63, 100, 115, 160 newts, see salamanders
- effects on kidney 170 newt water drive response 64, 176, 183
--urinary bladder 171, 178 nitrogen metabolism 39
see also neurohypophysial hormones -of amphibians 181
melatonin 47, 125 -birds 113
metabolism, of hormones 51 -fishes 220
migration 64, 110, 130, 152 - reptiles 133
- hormones influencing, in amphibians 64, see also aestivation, ammonia, urea, uric
183 acid
--birds 119, 130 noradrenaline 71, 88, 170, 176, 193, 198,213,
--fishes 195,212,215 224,230
milk 97,110
mineralocorticoids 57,68
mitochondria- rich cells 26, 31, 33,208, oesophagus, role in desalination in fish 29,
224,230 201
monotremes 97 opossum 75,98, 100,103
moulting 168 origin of vertebrates, relation to
mucous glands 24 osmoregulation 41
- excretory role in hagfish 230 ornithine-urea cycle 39, 43, 181, 220
-in amphibian skin 167, 176 osmolytes 5, 7, 35, 42, 181,228
- in fish gills and skin 26, 198 osmosis 10
mudpuppy 160,163,168,170,174,175,176, ostracoderms 41,42
181 ostrich 119, 128, 129
oxygen consumption, and water loss 9, 88,
97,99,138,167
nasal salt glands, see salt glands - thyroid hormone 76
native (marsupial) cat 99 see also respiration, temperature
natriferic effect, of neurohypophysial regulation
hormones 175,178 oxytocin 62, 97, 100, 111
Na-K-ATPase, see sodium-potassium
activated ATPase
natriuretic peptides 69, 72 panting 25, 87, 88, 102, 118
- distribution and effects, in amphibians see also temperature regulation
162, 168 parr, salmon 76, 196,212,215
- -birds 116, 124 parrots 116, 121, 129, 132
--fish 33, 72, 192, 193,201,202,205,213, see also budgerygah
217,223,225,226,230 pars distalis 60, 61
- - mammals 72, 96 pars intermedia 60, 61
neural lobe 61,107,108,160 pars nervosa 60, 61
neurohypophysectomy, effects, in amphibians "pelvic patch" (amphibian skin) 164, 166,
170 167,175,185
-birds 120 pharynyx 145,148
-mammals 102, 107 phenypressin 100
- reptiles 141 phosphatidylinositol 4,5-bisphosphate (PIP,)
neurohypophysial hormones 62 54
- in amphibians 160 phospholipase C (PLC) 54, 68, 72, 79,214
-birds 114 pigeons 96, 116, 121, 123, 129, 130
-fishes 191 pituitary gland 60
-mammals 62, 97, 99, 106 plasma, concentrations of solutes in
- reptiles 134 vertebrates 6

289
-volume 5, 96, 116, 188 -thyroid hormone 215
platypus 97,98 - vasopressin 53, 63, 100
potassium -vasotocin 54, 63, 122, 141, 170,214
-and adrenalectomy 103, 146, 180 rectal caecae (in birds) 126
- effects of aldosterone on 69, 84, 93 rectal (salt) gland 32, 33, 222, 225
- - in body fluids 6, 7 reed frogs 24,41,167
--faeces 93 release, of hormones 50
--saliva 92 renal portal systems, in vertebrates 35, 140,
- - salt gland secretions 32, 148, 148 168
--sweat 91 renal tubule, see kidneys
--urine 38 renin 66
- exchange in fish 206 - and formation of angiotensin 66
potassium channels 13, 84 -in amphibians 162
potassium transport 15, 30 -birds 115
see also, sodium-potassium activated -fishes 192,205
ATPase - mammals 111
pregnancy, see reproduction - reptiles 134
progesterone 184 see also angiotensin
prolactin 55, 64, 116, 127, 176 reproduction, effects on salt and water 90,
- distribution in vertebrates 116, 136, 162, 91,130,152,182,184
195,223,227 respiration, and water loss, in birds 117
- effects of lack, in freshwater adaptation -mammals 88
203,212,218 - reptiles 138
- crop sac (pigeon) 116, 131 see also oxygen consumption, temperature
- mammary glands 64 regulation
-newt "water-drive" 64, 176, 183 renin-angiotensin system 66, 99, 109, 115,
- oesophagus 201 134,162,180,192,223
- secretion in fresh water 212, 213 see also angiotensin II, renin
-sodium permeability of gills 212 rumen 29
proopiomelanocortin (POMC) 50, 65
protochordates 41, 55, 194
salamanders and newts 158, 162, 163, 164,
165,166,169,171,172,174,175,176,177,
quail 120, 121, 129 179, 180, 183
quokka 101, 103 saliva, see salivary glands
salivary glands 91
-secretion
rabbits 29, 90, 93, 94,96, 109 - - composition 92
Ras protein 55, 83 - - - effects of adrenalectomy 92
rats 107 - - - adrenocorticosteroids 92
rays 221 - - - urea content 89
receptors 46 - -in temperature regulation 93, 102
- adrenocorticotropic hormone 53 salmon and trout 188, 193, 195, 196, 197,
-adrenaline 53, 54, 72, 193,213 205,211,212,214,215,217,219
- angiotensin II 54, 67, 96, 218, 224 salt glands
- cortisol 211 - distribution 32
- glucocorticoid (GR) 56, 57, 70 --in birds 124
- growth hormone 55 - - fish 222, 223, 225
- guanylin 56, 76 - - reptiles 148
- !a-hydroxycorticosterone 224 - secretion
- IGF-I 54 --composition 32, 149,223
-mineralocorticoid (MR) 57, 70, 150 - - effect of acetylcholine 125
-natriuretic hormone 56, 74, 96, 125, 178, - - adrenaline 125, 150
213,218, 224,230 - - angiotensin II 125
- prolactin 55, 64,212 - - adrenocorticosteroids 125

290
- - melatonin 125 - appearance in tadpole skin 184
- - natriuretic peptides 125, 226 - chloride transport 16, 27, 216
- - plasma concentration 124 - sodium transport 12
- -vasoactive intestinal peptide 125, ISO, -in gills 27,208,209,210,211,212, 213,
226 214,215,224
- size, effect of salt diet 125, 127 - intestine 30, 202
see also, rectal gland -kidney 37, 77,218
sand rat 86, I 06 - salt glands 33, 226
sandgrouse 128, 131 -skin, amphibian 175
savannah sparrow 120, 123, 129 - tissue levels, effects of
seals II 0, Ill adrenocorticosteroids 57, 70, 83,210
sea birds 33, 124, 128, 123 - catecholamines 214
see also gulls -prolactin 213
sea snakes 133, 145, lSI -thyroid hormone 77, 175,215
"seat patch down" behaviour (in amphibians) sodium depletion 92
185 - effects of diet 87, 95, 105
seritocin 161 - in frogs in distilled water 173, 186
sgk protein 83 --during hibernation 186
sharks and rays 35, 221, 222, 227 see also adrenalectomy, hypophysectomy
sheep 29,90,91,96,105 sodium excess
skin 23, 163 - due to drinking saline and sea-water 29,
- role in salt metabolism, of amphibians 32, 86, 95, 110, 129, 199
173, 174, 186 - - diet 86, 93, l!O
- - fishes 198, 207 - effects on salt gland secretion 32
--mammals 110 - in teleosts 199
- - reptiles 144 see also hypernatremia
- - in water metabolism, of amphibians somatolactin 64, 195
163, 185 spadefoottoad 157,164,169,181,183
- --birds 118 sparrows 121, 122, 123, 132
- - - fishes 198, 230 sticklebacks 206, 212, 215
- - - mammals II 0 supraoptic nucleus 61
- -- reptiles 137, 144 sweat glands 87,91
- - in temperature regulation liB synthesis, of hormones 49
see also sweat glands, temperature
regulation
smolt, salmon 76, 196,212,215 tadpoles 159, 174, 175, 183, 184
snakes 134, 137, 139, 140, 141, 142, 146, 147 temperature regulation
see also sea snakes -and behaviour 25, 99, 118
sodium - - evaporative water loss 11, 24
- in body fluids 6, 7 - - salivation 93, I 02
- diet 86, 94, 95 -- sweating 87, 102
- saliva 91 - in birds liS
- salt gland secretion 32, 149 --mammals 87, 88, 97, 99, 102
- sweat 91, 92 see also body temperature, gular flutter,
see also active transport, cloaca, colon, hyperthermia, oxygen consumption,
gills, intestine, kidney, sodium- panting, respiration
potassium activated ATPase, sodium thirst 29, 74, 95, 109
depletion, sodium excess, skin, sweat thyroid gland 76, 194
glands, urine, urinary bladder see also thyroid hormones
sodium appetite 29, 74, 95, 96, 103, 109, 128, thyroid hormones (triiodothyronine,
129 thyroxine) 76, 194
sodium channels 13, 30, 175 -and fish salinity tolerance 215
see also ENaC -metamorphosis in tadpoles 76, 174, 184,
sodium-potassium activated ATPase -morphogenetic actions 76, 184, 194
(Na-K ATPase) 12, 15 thyroid-stimulating hormone (TSH) 76

291
thyroxine, see thyroid hormones see also adrenaline, aldosterone, kidney,
tilapia 188, 195,206,212,215,220 mesotocin, natriuretic peptide,
toadfish 195,197,206,217,219,220,221 vasopressin, vasotocin
toads, see frogs and toads uroguanylin 75
tortoise, see turtles and tortoises urophysis 77, 194
tree frogs 41, 157, 166, 167, 175, 182 urotensin I 77, 192, 194
triiodothyronine, see thyroid hormones urotensin II 77, 194
trimethylamine oxide (TMAO) 5, 7, 181,
222,228
trout, see salmon valitocin 63
turtles and tortoises 3, 4, 31, 40, 136, 138, vasae rectae 35, 67, 80, 89
141, 142, 143, 144, 145, 146, 147, 148, 150, vasoactive intestinal peptide (VIP) 125,
151, 152 150,226
see also desert tortoise vasopressin (ADH, AVP) 18, 62, 91
- concentrations in neurohypophysis 97,
102, 108
urea 7, 40 - - in blood plasma 102
- and urinary water loss 40 - - effects of dehydration 102, 107, 111
- concentrations in body fluids during --distribution in mammals 97,106,111
aestivation 181 --of lysine-vasopressin 100, 107
-crab-eating frog 157, 159, 181 see also neurohypophysial hormones,
- coelacanth 40, 220 urine
- desert toads 181 vasotocin (AVT) 63, 114, 130, 160, 191,229
- freshwater rays 227 - concentrations in neurohypophysis 114,
- lungfish 220 121,160,205
-saliva 89 - effects on, blood flow in gills 214
- sharks and rays 35, 222, 227 - - blood pressure 170
-Xenopus 181 --glomeruli 121, 141, 142, 169,203
- permeability, of amphibian skin to 182 --oviduct 115, 142, 152, 183
--gills 221,224 - -skin, amphibian 166, 175, 184
- - kidney tubule 18 --sodium exchanges 175, 177, 217
- - urinary bladder 182 - - urea p ermeability 182, 221
urea transporters 14, 18, 80,221,224,225 --urinary bladder, amphibian 171, 182
uric acid 40 --urine flow 121, 140, 141, 169,217
- and urinary water loss 40 -release 63, 121, 122, 166, 173, 205
-excretion, in amphibians 182 VIP, see vasoactive intestinal peptide
- - birds 113, 120
- - reptiles 140, 142
see also nitrogen metabolism wallabies 103
urinary bladder 31 see also kangaroos, quokka
- effects of,adrenaline 179 water b alance response (in amphibians)
- - aldosterone 147, 179 160
-roles in water and salt metabolism 143, water "pumps" 12, 19
147, 171, 178,218 "water seeking" behaviour in amphibians
urine 36, 37, 119 185
-concentrations 36, 102, 104 see also newt water drive response
- effects of, adrenaline 170 whales 110, 111
- - ·aldosterone 94, 146 "wiping" behaviour (in amphibians) 24, 167
-- neurohypophysial hormones 62, 91,
102, 107
- in amphibians 168 Xenopus (aquatic toad) 161, 162, 163, 164,
-birds 120 165, 166, 167, 170, 171, 175, 178,181
-fish 203
-mammals 99, 102, 107
- reptiles 140 zebra finch 116, 119, 129

292