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配体特异性受体状态:对阿片受体信号传导和调节的影响。

Ligand-specific receptor states: implications for opiate receptor signalling and regulation.

作者信息

Piñeyro Graciela, Archer-Lahlou Elodie

机构信息

Département de Pharmacologie, Faculté de Médecine, Université de Montréal, Canada.

出版信息

Cell Signal. 2007 Jan;19(1):8-19. doi: 10.1016/j.cellsig.2006.05.026. Epub 2006 Jun 7.

Abstract

Opiate drugs produce their effects by acting upon G protein coupled receptors (GPCRs) and although they are among the most effective analgesics available, their clinical use is restricted by unwanted side effects such as tolerance, physical dependence, respiratory depression, nausea and constipation. As a class, opiates share a common profile of unwanted effects but there are also significant differences in ligand liability for producing these actions. A growing number of studies show that GPCRs may exist in multiple active states that differ in their signalling and regulatory properties and which may distinctively bind different agonists. In this review we summarize evidence supporting the existence of multiple active conformations for MORs and DORs, analyze information favouring the existence of ligand-specific receptor states and assess how ligand-selective efficacy may contribute to the production of longer lasting, better tolerated opiate analgesics.

摘要

阿片类药物通过作用于G蛋白偶联受体(GPCRs)产生其效应,尽管它们是现有的最有效的镇痛药之一,但其临床应用受到诸如耐受性、身体依赖性、呼吸抑制、恶心和便秘等不良副作用的限制。作为一类药物,阿片类药物具有共同的不良作用特征,但在产生这些作用的配体倾向方面也存在显著差异。越来越多的研究表明,GPCRs可能以多种活性状态存在,这些状态在信号传导和调节特性方面有所不同,并且可能特异性地结合不同的激动剂。在这篇综述中,我们总结了支持MORs和DORs存在多种活性构象的证据,分析了支持存在配体特异性受体状态的信息,并评估了配体选择性效力如何有助于产生更持久、耐受性更好的阿片类镇痛药。

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