Muscarinic acetylcholine receptor knockout mice: Novel phenotypes and clinical implications

被引:298
作者
Wess, J [1 ]
机构
[1] NIDDKD, Mol Signalling Sect, Bioorgan Chem Lab, DHHS, Bethesda, MD 20892 USA
关键词
gene targeting; muscarinic agonist; muscarinic antagonist; parasympathetic nervous system; signal transduction;
D O I
10.1146/annurev.pharmtox.44.101802.121622
中图分类号
R9 [药学];
学科分类号
1007 ;
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 in-sights gained from these studies should prove instrumental for the development of novel classes of muscarinic drugs.
引用
收藏
页码:423 / 450
页数:28
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