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G蛋白偶联受体的超生理效应:迷信还是超级激动剂?

Supra-physiological efficacy at GPCRs: superstition or super agonists?

作者信息

Langmead Christopher J, Christopoulos Arthur

机构信息

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3052, Australia.

出版信息

Br J Pharmacol. 2013 May;169(2):353-6. doi: 10.1111/bph.12142.

Abstract

The concept of 'super agonism' has been described since the discovery of peptide hormone analogues that yielded greater functional responses than the endogenous agonists, in the early 1980s. It has remained an area of debate as to whether such compounds can really display greater efficacy than an endogenous agonist. However, recent pharmacological data, combined with crystal structures of different GPCR conformations and improved analytical methods for quantifying drug action, are starting to shed light on this phenomenon and indicate that super agonists may be more than superstition.

摘要

自20世纪80年代初发现能产生比内源性激动剂更强功能反应的肽激素类似物以来,“超级激动作用”的概念就已被描述。这类化合物是否真的能表现出比内源性激动剂更高的效力,一直是一个存在争议的领域。然而,最近的药理学数据,结合不同GPCR构象的晶体结构以及改进的药物作用量化分析方法,开始为这一现象带来启示,并表明超级激动剂可能并非只是迷信。

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