v5.1.0.3
Cicer data from the Legume Information System
| Type | Family |
| Description | Muscarinic acetylcholine receptors are members of rhodopsin-like G-protein coupled receptor family. They play several important roles; they mediate many of the effects of acetylcholine in the central and peripheral nervous system and modulate a variety of physiological functions, such as airway, eye and intestinal smooth muscle contraction, heart rate and glandular secretions. The receptors have a widespread tissue distribution and are a major drug target in human disease. They may be effective therapeutic targets in Alzheimer's disease, schizophrenia, Parkinson's disease and chronic obstructive pulmonary disease [ , ]. There are five muscarinic acetylcholine receptor subtypes, designated M1-5 [ , , , , ]. The family can be further divided into two broad groups based on their primary coupling to G-proteins. M2 and M4 receptors couple to the pertussis-toxin sensitive Gi proteins, whereas M1, M3 and M5 receptors couple to Gq proteins [, ], which activate phospholipase C. The different subtypes can also couple to a wide range of diverse signalling pathways, some of which are G protein-independent [, , ].All subtypes seem to serve as autoreceptors [ ], and knockout mice reveal the important neuromodulatory role played by this receptor family [, , ].The muscarinic acetylcholine M5 receptor is primarily found in the CNS [ , , ], but is also found in esophageal smooth muscle [] and in the heart []. Binding of acetylcholine to the receptor triggers a number of cellular responses, such as adenylate cyclase inhibition [], phosphoinositide degradation [], and potassium channel modulation []. The receptor has been shown to stimulate gastric acid secretion []. |
| Short Name | Musac_Ach_M5_rcpt |