作为中枢神经系统药物靶点的毒蕈碱型乙酰胆碱受体。

Muscarinic acetylcholine receptors as CNS drug targets.

作者信息

Langmead Christopher J, Watson Jeannette, Reavill Charlie

机构信息

Psychiatry Centre of Excellence for Drug Discovery, GlaxoSmithKline, Third Avenue, Harlow, Essex, CM19 5AW, UK.

出版信息

Pharmacol Ther. 2008 Feb;117(2):232-43. doi: 10.1016/j.pharmthera.2007.09.009. Epub 2007 Dec 20.

Abstract

Muscarinic acetylcholine receptors (mAChRs) are widely expressed in the CNS where they control a variety of neuronal functions. Due to their roles in a number of CNS processes, mAChRs have long been a target of the drug discovery industry; however, the only mAChR ligands approved for use in the clinic are non-selective antagonists for the treatment of Parkinson's disease. This article briefly reviews recent progress made in mAChR drug discovery for Alzheimer's disease (AD), schizophrenia and Parkinson's disease, with particular emphasis on novel target validation, as well as highlighting novel indications such as drug addiction.

摘要

毒蕈碱型乙酰胆碱受体(mAChRs)在中枢神经系统中广泛表达,在那里它们控制着多种神经元功能。由于它们在许多中枢神经系统过程中发挥作用,mAChRs长期以来一直是药物研发行业的靶点;然而,唯一被批准用于临床的mAChR配体是用于治疗帕金森病的非选择性拮抗剂。本文简要回顾了在针对阿尔茨海默病(AD)、精神分裂症和帕金森病的mAChR药物研发方面取得的最新进展,特别强调了新靶点的验证,同时也突出了诸如药物成瘾等新的适应症。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索