P2受体药理学分析的冒险

Malbinder S. Fagura , Gavin E. Jarvis , Iain G. Dougall , Paul Leff
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引用次数: 9

摘要

P2受体的药理学分类要归功于Geoff Burnstock及其后继者的开创性努力,这些研究主要是在生理实验系统中进行的。近年来,分子生物学技术越来越多地应用于P2受体的研究,但由于缺乏有效的、选择性的激动剂或拮抗剂配体,其药理分析的进展受到限制。这导致了一个分类方案,这在本质上很大程度上是结构性的,相对较少的贡献来自药理学。我们在这一领域的努力一直是为了发现配体,通过配体可以推进P2受体的药理分析和定义,最终目标是设计治疗剂。本文将描述我们在这个具有挑战性但有益的领域的一些经验。
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Adventures in the pharmacological analysis of P2 receptors

The pharmacological classification of P2 receptors owes its origin to the pioneering efforts of Geoff Burnstock and those who followed him, research that was conducted primarily in physiological experimental systems. Over recent years, the techniques of molecular biology have been increasingly applied in the study of P2 receptors while, at the same time, advances in their pharmacological analysis have been limited by a lack of potent and selective agonist or antagonist ligands. This has resulted in a classification scheme which is largely structural in nature, with relatively little contribution from pharmacology. Our endeavours in this area have been directed towards the discovery of ligands with which the pharmacological analysis and definition of P2 receptors could be advanced, the ultimate goal being the design of therapeutic agents. This article will describe some of our experiences in this challenging but rewarding area.

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