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[G蛋白偶联蛋白酶受体PAR(蛋白酶激活受体)作为药物研发的新靶点]

[The G protein-coupled protease receptor PAR (protease-activated receptor) as a novel target for drug development].

作者信息

Kawabata A

机构信息

Department of Pathophysiology & Therapeutics, Faculty of Pharmaceutical Sciences, 3-4-1 Kowakae, Higashi-Osaka 577-8502, Japan.

出版信息

Yakugaku Zasshi. 2001 Jan;121(1):1-7. doi: 10.1248/yakushi.121.1.

Abstract

The protease-activated receptor (PAR) is the family of G protein-coupled, seven transmembrane domain receptors, currently consisting of four members, PARs 1-4. The activation of PARs occurs by proteolytic unmasking of the N-terminal cryptic receptor-activating tethered ligand. In the past decade since the cloning of PAR-1, physiological roles that PARs play have been gradually understood and are now considered extremely extensive and important. This review describes physiological and/or pathophysiological roles of PARs in the circulatory, digestive, respiratory and central nervous systems, on the basis of our works and of those achieved by other research groups. The future perspective of studies on PARs is also discussed, focusing on the possibility of clinical application of PAR-targeted drugs.

摘要

蛋白酶激活受体(PAR)是G蛋白偶联的七跨膜结构域受体家族,目前由四个成员组成,即PAR-1至PAR-4。PAR的激活通过对N端隐蔽的受体激活拴系配体进行蛋白水解暴露来实现。自PAR-1克隆以来的过去十年中,PAR发挥的生理作用已逐渐被了解,目前被认为极其广泛且重要。本综述基于我们的研究工作以及其他研究小组所取得的成果,描述了PAR在循环系统、消化系统、呼吸系统和中枢神经系统中的生理和/或病理生理作用。还讨论了PAR研究的未来前景,重点关注PAR靶向药物临床应用的可能性。

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