毒蕈碱乙酰胆碱受体
神经化学
毒蕈碱乙酰胆碱受体M4
神经科学
毒蕈碱乙酰胆碱受体M3
生物
基因剔除小鼠
乙酰胆碱
表型
毒蕈碱乙酰胆碱受体M1
受体
毒蕈碱乙酰胆碱受体M2
毒蕈碱乙酰胆碱受体M5
突变体
中枢神经系统
基因
药理学
遗传学
标识
DOI:10.1146/annurev.pharmtox.44.101802.121622
摘要
Muscarinic acetylcholine receptors (mAChRs; M 1 –M 5 ) play key roles in regulating the activity of many important functions of the central and peripheral nervous system. Because of the lack of ligands endowed with a high degree of receptor subtype selectivity and the fact that most tissues or cell types express two or more mAChR subtypes, identification of the physiological and pathophysiological roles of the individual mAChR subtypes has proven a difficult task. To circumvent these difficulties, several laboratories recently employed gene-targeting techniques to generate mutant mouse strains deficient in each of the five mAChR subtypes. Phenotyping studies showed that each mutant mouse line displayed characteristic physiological, pharmacological, behavioral, biochemical, or neurochemical deficits. The novel insights gained from these studies should prove instrumental for the development of novel classes of muscarinic drugs.
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