Pronounced pharmacologic deficits in M2 muscarinic acetylcholine receptor knockout mice

被引:291
|
作者
Gomeza, J
Shannon, H
Kostenis, E
Felder, C
Zhang, L
Brodkin, J
Grinberg, A
Sheng, H
Wess, J
机构
[1] NIDDKD, Bioorgan Chem Lab, Bethesda, MD 20892 USA
[2] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
[3] NICHHD, Lab Mammalian Genes & Dev, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.96.4.1692
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Members of the muscarinic acetylcholine receptor family (M1-M5) are known to be involved in a great number of important central and peripheral physiological and pathophysiological processes. Because of the overlapping expression patterns of the M1-M5 muscarinic receptor subtypes and the lack of ligands endowed with sufficient subtype selectivity, the precise physiological functions of the individual receptor subtypes remain to be elucidated. To explore the physiological roles of the M2 muscarinic receptor, we have generated mice lacking functional M2 receptors bg using targeted mutagenesis in mouse embryonic stem cells. The resulting mutant mice were analyzed in several behavioral and pharmacologic tests. These studies showed that the M2 muscarinic receptor subtype, besides its well documented involvement in the regulation of heart rate, plays a key role in mediating muscarinic receptor-dependent movement and temperature control as well as antinoeiceptive responses, three of the most prominent central muscarinic effects, These results offer a rational basis for the development of novel muscarinic drugs.
引用
收藏
页码:1692 / 1697
页数:6
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