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毒蕈碱受体——特性、偶联与功能

Muscarinic receptors--characterization, coupling and function.

作者信息

Caulfield M P

机构信息

Department of Pharmacology, University College London, U.K.

出版信息

Pharmacol Ther. 1993 Jun;58(3):319-79. doi: 10.1016/0163-7258(93)90027-b.

Abstract

At least five muscarinic receptor genes have been cloned and expressed. Muscarinic receptors act via activation of G proteins: m1, m3 and m5 muscarinic receptors couple to stimulate phospholipase C, while m2 and m4 muscarinic receptors inhibit adenylyl cyclase. This review describes the localization, pharmacology and function of the five muscarinic receptor subtypes. The actions of muscarinic receptors on the heart, smooth muscle, glands and on neurons (both presynaptic and postsynaptic) in the autonomic nervous system and the central nervous system are analyzed in terms of subtypes, biochemical mechanisms and effects on ion channels, including K+ channels and Ca2+ channels.

摘要

至少已克隆并表达了五种毒蕈碱受体基因。毒蕈碱受体通过激活G蛋白发挥作用:M1、M3和M5毒蕈碱受体与刺激磷脂酶C偶联,而M2和M4毒蕈碱受体则抑制腺苷酸环化酶。本综述描述了五种毒蕈碱受体亚型的定位、药理学和功能。从亚型、生化机制以及对离子通道(包括钾通道和钙通道)的影响方面,分析了毒蕈碱受体在自主神经系统和中枢神经系统中对心脏、平滑肌、腺体以及神经元(突触前和突触后)的作用。

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