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Chapter: Biochemical Pharmacology : G protein-coupled receptors

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Pharmacology of cholinergic synapses

The nicotinic acetylcholine receptor is found in the motor endplate of the skeletal muscle, and in both the sympathetic and the parasympathetic ganglia of the periph-eral autonomic system.

Pharmacology of cholinergic synapses

As we have seen [in a previous chapter], acetylcholine oc-curs in synapses in both the somatic and the autonomic ner-vous system. The nicotinic acetylcholine receptor is found in the motor endplate of the skeletal muscle, and in both the sympathetic and the parasympathetic ganglia of the periph-eral autonomic system. Muscarinic acetylcholine receptors are found at the endings of all secondary neurons within the parasympathetic part of the peripheral autonomous system. In addition, acetylcholine receptors of both types also oc-cur in the brain. Drugs with a useful degree of selectivity for each of these targets are available and used in practical medicine. Selectivity is based on two principles:

 

1.  Receptor type and subtype specificity of agonists or antagonists, and

 

2.  Exclusion by the blood brain barrier of drugs intended for peripheral action.

 

One particular feature of cholinergic synapses is the mode of transmitter inactivation. While with most transmit-ters this is accomplished by presynaptic transmitter re-uptake, acetylcholine is cleaved extracellularly by acetyl-cholinesterase. This enzyme is located on the postsynaptic membrane, right next to the receptors (Figure 9.1). Its ac-tivity is very high, so that the rate-limiting event in acetyl-choline inactivation is not cleavage but dissociation from the receptor. Besides the direct receptor agonists and an-tagonists, blockers of cholinesterase (also referred to as `in-direct agonists') are an additional class of drugs that will modulate the effectiveness of transmission in cholinergic synapses.



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