Chapter 3 discusses the mechanisms of neural transport and the role of microtubules in neuron function, including anterograde and retrograde transport. It highlights the importance of sodium-potassium and calcium pumps in maintaining ion balance, as well as the impact of microtubules on conditions like Alzheimer's disease. Additionally, it covers the processes of action potentials, neurotransmitter release, and the integration of excitatory and inhibitory signals in neuronal communication.
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BIOPSYCH Chapter-3
Chapter 3 discusses the mechanisms of neural transport and the role of microtubules in neuron function, including anterograde and retrograde transport. It highlights the importance of sodium-potassium and calcium pumps in maintaining ion balance, as well as the impact of microtubules on conditions like Alzheimer's disease. Additionally, it covers the processes of action potentials, neurotransmitter release, and the integration of excitatory and inhibitory signals in neuronal communication.
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Chapter 3 (continuation) • Movement along the microtubules
from the cell body to the axon
terminal is known as anterograde transport, and movement back to the cell body from the periphery of the neuron is known as retrograde transport
The two most important pumps in neurons:
1. Sodium-potassium pumps help
maintain the differences in chemical composition between the intracellular and extracellular fluids. - do a “prisoner exchange” across the neural membrane by sending three • Microtubules have been implicated in sodium ions out of the cell while the development of Alzheimer’s collecting two potassium ions from disease the extracellular environment. o characterized initially by - This process comes at a high cost to memory loss, followed by the neuron. Possibly as much as 20 to progressive decline in 40 percent of the energy required by cognitive and physical the brain is used to run the sodium- functions, eventually leading potassium pumps to death. o the presence of 2. Calcium pumps perform a similar function, neurofibrillary tangles although they do not collect another type of consisting of a protein called ion in exchange for the calcium they pump tau. out of the cell. o In a healthy brain, tau Neural Cytoskeleton connects adjacent microtubules and holds them • Microtubules, which are formed in in place. In Alzheimer’s the shape of hollow tubes with a disease, the tau levels diameter of about 25 nm become elevated (Baas & (nanometers). Qiang, 2005). o responsible for the o In response, an affected movement of various neuron adds molecules of materials within the cell. phosphate to the tau protein, • Neurofilaments provide structural which causes it to disconnect support, whereas microfilaments may from the microtubules. be involved with structural changes associated with learning. whereas the relatively positive exterior attracts • Diffusion force that moves molecules them. Chloride finds its from areas of high concentration to equilibrium. areas of low concentration. • Sodium is found in greater • Diffusion pressure moves molecules concentration on the outside than on along a concentration gradient from the inside of the cell. areas of high concentration to areas o But unlike the cases of of low concentration. potassium and chloride, • Another important cause of electrical force is not working movement of molecules is electrical against diffusion but in the force. As you may already know from same direction. playing with magnets, opposite signs o The positive sodium ions attract and like signs repel. Ions work should be very attracted to the same way. the negative interior of the • Potassium is found in larger cell. With both diffusion concentrations on the inside of the pressure and electrical force cell than on the outside. pushing sodium into the cell, • Diffusion would move the potassium how do we account for the ions along their concentration fact that most of the sodium gradient from the inside (the area of is found on the outside? The higher concentration) to the outside answer lies in the nature of (the area of lower concentration) our very important neural • However, diffusion pressure is membrane. balanced by electrical force in this case. • Potassium is a positively charged ion. As such, it is content to stay in the negative environment on the inside of the cell and reluctant to venture into the relatively positive environment outside the cell. The net distribution of potassium reflects a balance, or equilibrium, between diffusion pressure and electrical force. • Chloride is the mirror image of potassium. o Chloride, a negatively charged ion, is more concentrated outside the cell than inside it. Therefore, diffusion pressure works to push chloride into the cell. o Once again, diffusion is counteracted by electrical force. The negative interior of • Action potentials originate in the axon the cell repels the negatively hillock and then travel the length of charged chloride ions, the axon to the axon terminal. • The arrival of action potentials at the • Receiving neurons receive multiple axon terminal signals the release of messages from other neurons, and neurotransmitters from the synaptic these messages determine if an vesicles. action potential occurs or not. • Molecules of neurotransmitter diffuse • Note how the axon terminals of across the synaptic gap, where they sending neurons almost completely interact with receptors embedded in cover the cell body of the receiving the dendrite of the adjacent neuron. neuron. • Major Neurotransmitters: o Serotonin o Acetylcholine (ACh) o Dopamine (DA) o Norepinephrine (NE) o Epinephrine (adrenaline) o GABA (gamma aminobutyric acid) o Endorphins
Neural Bases of Behavior: Neural
Communication
• Within a neuron, communication
occurs through an action potential (neural impulse that carries information along the axon of a neuron). Neural Bases of Behavior: Receptor Sites • Between neurons, communication • normal message occurs through transmission of neural • blocked message (wrong shape) information across a synapse by • agonistic drugs mimic shape and neurotransmitters (chemicals enhance neurotransmitter released by neurons that alter activity • antagonistic drugs fill the site and in other neurons). block neurotransmitter Synapse Neural Conduction and Synaptic Transmission
• Resting Membrane Potential (RMP)
o The difference in electrical charge between the inside and the outside of the cell o The neuron is unexcited, unstimulated, therefore not transmitting any impulse 2. Decremental = decrease in amplitude as (polarized state = -70mv) they travel through a neuron
Integration of Post Synaptic Potential and
Generation of Action Potentials
• Whether or not a neuron fires is
determined by the net effect of their activity. • It depends on the balance between the excitatory and inhibitory signals reaching its axon hillock (the conical structure at the junction between the cell body and the axon) Generation and Conduction of Post Synaptic • If the sum of the depolarization and Potential hyperpolarization reaching the axon • When neurons fire, they release from hillock at anytime is sufficient to their terminal buttons chemicals depolarize the membrane to a level is called neurotransmitter. referred to as THRESHOLD OF • When neurotransmitter molecules EXCITATION (-65mv) bind to post synaptic receptors, they • Action Potential is generated at the may DEPOLARIZE the receptive axon hillock membrane (decrease the RMP from - • Graded EPSP and IPSP are added 70mv to -67mv) or they may together as it reaches the axon hillock HYPERPOLARIZE the receptive and decides to fire or not on the basis membrane (increase RMP from -70mv of their SUM to -72 mv) • Adding or combining a number of • Post synaptic depolarizations are individual signals into one overall called Excitatory Post-synaptic signal is called INTEGRATION. Potential (EPSP) – increase likelihood • Neurons integrate incoming signals that the neuron will fire an impulse through: (less negative) 1. Spatial Summation – • Post synaptic hyperpolarizations are involve adding up several called Inhibitory Post-synaptic EPSP & IPSP coming from Potential (IPSP) – decrease the different synaptic sites likelihood that the neuron will fire an 2. Temporal Summation – impulse (more negative) involve repeated stimulation • Both EPSP and IPSP are graded of one synaptic site responses – amplitudes of both are proportional to the intensity of signals THE IONIC BASIS of Action Potentials that elicit them. o Weak signal = weak impulse; • Action potentials are voltage strong = strong impulse activated or regulated through the action of voltage activated ion Transmission of post synaptic potentials has channels (ion channels that open or two characteristics: close in response to changes in the level of membrane potential) 1. Rapid = instantaneous • EXOCYTOSIS – the process whereby a neurotransmitter is released • Absolute Refractory Period (period in millisecond when irritability is zero) o Cannot be stimulated or respond again if second stimulus is applied • Relative Refractory Period (the period during which it is possible to fire the neuron again, but only by applying higher than normal levels of stimulation o Need a stronger stimulus to fire