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历史回顾:G蛋白偶联受体的负性效能与组成性活性

Historical review: Negative efficacy and the constitutive activity of G-protein-coupled receptors.

作者信息

Costa Tommaso, Cotecchia Susanna

机构信息

Department of Pharmacology, Istituto Superiore di Sanità, Italy.

出版信息

Trends Pharmacol Sci. 2005 Dec;26(12):618-24. doi: 10.1016/j.tips.2005.10.009. Epub 2005 Nov 2.

Abstract

The idea that a receptor can produce signalling without agonist intervention and that several antagonists can be 'active' in repressing such spontaneous activity is contained in the concept of ligand-induced conformational changes. Yet, this idea was neglected by pharmacologists for many years. In this article, we review the events that brought inverse agonism and constitutive activity to general attention and made this phenomenon a topic of current research. We also suggest a classification of antagonists based on the cooperativity that links their primary site of interaction with other functional domains of the receptor.

摘要

受体能够在没有激动剂干预的情况下产生信号传导,并且几种拮抗剂能够在抑制这种自发活性方面具有“活性”,这一观点包含在配体诱导的构象变化概念中。然而,多年来药理学家一直忽视了这一观点。在本文中,我们回顾了使反向激动作用和组成性活性引起广泛关注并使其成为当前研究课题的相关事件。我们还基于将拮抗剂与受体其他功能域的主要相互作用位点联系起来的协同性,提出了一种拮抗剂分类方法。

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