Rumipro Paper
Rumipro Paper
CALVES
Abstract
Introduction
The animals were divided into two groups A and B, comprised of five calves
each, while Group C had two calves. Acid indigestion was induced in all the
twelve calves by oral dosing with wheat flour @ 30 gm/kg body weight.
Twelve hours after induction of acid indigestion, the following treatments were
adopted:
a. Calves of Group A received RUMIPRO @ one bolus twice daily for three
days.
b. The calves of Group B were given sodium bicarbonate @ 100 mg/kg body
weight for two days along with RUMIPRO as above.
c. The calves of Group C served as untreated control.
About 100 ml rumen liquor was collected from each calf before induction of acid
indigestion and after that at different intervals. The strained rumen liquor was
subjected to physical, biochemical and microbial analysis. The physical
characteristics like colour, odour and consistency were studied using the method
described by Misra and Tripathy (1963). Motility of rumen liquor was graded
according to Misra et al. (1972), as vigorous (+++), moderate (++) and mild (+).
The pH of fresh rumen liquor was recorded using Elico-pH were estimated
according to the method described by Barnet and Reid (1961). The value was
expressed as mEq/L. For total protozoal count, the method described 4 by Moir
(1951) was followed and this was expressed as x10 4 /ml. The sedimentation
activity time (SAT) and glucose fermentation time (GFT) were determined
according to the procedure described by Chakrabarti (1989).
The ruminal and reticular contractions were recorded using both the fist and
stethoscope. In addition, frequency of urination and defecation and consistency
of faeces were noted. The appetite and general health of the calves were also
observed periodically.
Restoration of total protozoal count and also their motility indicated the
beneficial effectes of RUMIPRO on rumen protozoa. Significant increase in SAT
and reduction in GFT by 12 hrs of induction of acidic indigestion could be
ascribed to destruction and gross inactivity of normal microflora of rumen as
reported by Nicholas and Pen (1958), Rosenberger (1979), and Blood and
Radostits (1989). Complete restoration of GFT to normal by 36 hrs indicated
revival of microfloral activity of RUMIPRO therapy. However the SAT though
improved, did not reach normal even by 72 hrs. Rise in TVFA after administration
of RUMIPRO indicated the restoration of rumen microbial carbohydrate
fermentation.
Untreated control animals did not show any improvement in TVFA concentration.
Protozoal and bacterial activity of rumen returned to normal following therapy
with sodium bicarbonate and rumen cud transplant (Prasad and Rekib, 1975).
In untreated calves (Tables 1 and 2), the protozoal motility and total count were
much less than that in the RUMIPRO – trated groups. Some improvement in SAT
and GFT values were noted at much slower rate as compared to animals treated
with RUMIPRO. Rumeno-reticular movements and other clinical signs showed
improvement at slower rate. Combination of sodium bicarbonate with RUMIPRO
was helpful in restoring rumen pH only. The overall improvement remained as in
Group A, treated with RUMIPRO only.
Table 1
Microbial and Biochemical Observations in Rumen Acid Indigestion with RUMIPRO Treatment (Group - A)
Protoz Total
Rumen Reticular
Hr( oal protozoal SAT GFT TVFA(mEg/l Colou
pH contraction contraction Odour
s) motilit count (Min.) (ml/hr) ) rs
(Per 2 min.) (Per 2 min.)
y (x104 / ml)
7.38 ± 0.06 +3.4 (++ 1.82 ± 0.07 72.7 ± 9.59
0
(7.25) +)
6.34 ± 1.16 (6.5) 13.2 (12.5)
(2.25) (74.5)
3.33 (3.0) 3.66 (4.0) YG-B AR
Table 2
Microbial and Biochemical Observations in Rumen Acid Indigestion with RUMIPRO and Sodium Bicarbonate Treatment (Group
B).