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关于β(2)-肾上腺素能受体配体在哮喘治疗中的新观点。

New perspectives regarding β(2) -adrenoceptor ligands in the treatment of asthma.

机构信息

Department of Medicine, Duke University Medical Center, Durham, NC, USA.

出版信息

Br J Pharmacol. 2011 May;163(1):18-28. doi: 10.1111/j.1476-5381.2010.01178.x.

Abstract

In the last two decades several significant changes have been proposed in the receptor theory that describes how ligands can interact with G protein-coupled receptors (GPCRs). Here we briefly summarize the evolution of receptor theory and detail recent prominent advances. These include: (i) the existence of spontaneously active GPCRs that are capable of signalling even though they are unoccupied by any ligand; (ii) the discovery of ligands that can inactivate these spontaneously active receptors; (iii) the notion that a ligand may simultaneously activate more than one GPCR signalling pathway; and (iv) the notion that certain ligands may be able to preferentially direct receptor signalling to a specific pathway. Because the data supporting these receptor theory ideas are derived primarily from studies using artificial expression systems, the physiological relevance of these new paradigms remains in question. As a potential example of how these new perspectives in receptor theory relate to drug actions and clinical outcomes, we discuss their relevance to the recent controversy regarding the chronic use of β(2) -adrenoceptor agonists in the treatment of asthma.

摘要

在过去的二十年中,描述配体如何与 G 蛋白偶联受体(GPCR)相互作用的受体理论发生了一些重大变化。在这里,我们简要总结了受体理论的发展,并详细介绍了最近的突出进展。这些进展包括:(i)存在自发激活的 GPCR,即使它们未被任何配体占据,也能够进行信号传递;(ii)发现了可以使这些自发激活的受体失活的配体;(iii)一种配体可以同时激活多种 GPCR 信号通路的概念;和(iv)某些配体可能能够优先将受体信号导向特定通路的概念。由于支持这些受体理论观点的数据主要来自于使用人工表达系统的研究,因此这些新范例的生理学相关性仍存在疑问。作为受体理论新观点与药物作用和临床结果相关的潜在示例,我们讨论了它们与最近关于β(2)-肾上腺素能受体激动剂在哮喘治疗中的慢性使用的争议的相关性。

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