Kawabata Atsufumi
Department of Physiology and Pathophysiology, School of Pharmaceutical Sciences, Kinki University, Higashi-Osaka, Japan.
Nihon Yakurigaku Zasshi. 2003 Jun;121(6):411-20. doi: 10.1254/fpj.121.411.
Protease-activated receptors (PARs) are a family of G-protein-coupled-seven-trans-membrane-domain-receptors activated by specific proteases, consisting of four family members. PAR-2, a receptor activated by trypsin, tryptase or coagulation factors VIIa and Xa, is unevenly distributed throughout the mammalian body, modulating multiple physiological functions. In the gastrointestinal tract, PAR-2 is involved in gastric mucosal cytoprotection, smooth muscle motility modulation, salivary and pancreatic exocrine secretion, intestinal ionic transport, etc. In the circulatory system, endothelial PAR-2, upon activation, induces vascular relaxation by mechanisms dependent on nitric oxide or endothelium-derived hyperpolarizing factor (EDHF), resulting in hypotension in vivo. In the respiratory system, PAR-2 appears to play a dual role, being pro- and anti-inflammatory. In the nervous system, PAR-2 present in capsaicin-sensitive sensory neurons participates in processing of pain information. PAR-2 is thus involved in a variety of physiological and pathophysiological functions. PAR-2 is now considered one of the most important molecules as a target for drug development.
蛋白酶激活受体(PARs)是一类由特定蛋白酶激活的G蛋白偶联七跨膜结构域受体,由四个家族成员组成。PAR-2是一种由胰蛋白酶、类胰蛋白酶或凝血因子VIIa和Xa激活的受体,在哺乳动物体内分布不均,调节多种生理功能。在胃肠道中,PAR-2参与胃黏膜细胞保护、平滑肌运动调节、唾液和胰腺外分泌、肠道离子转运等。在循环系统中,内皮PAR-2激活后,通过依赖一氧化氮或内皮衍生超极化因子(EDHF)的机制诱导血管舒张,导致体内低血压。在呼吸系统中,PAR-2似乎发挥双重作用,具有促炎和抗炎作用。在神经系统中,存在于辣椒素敏感感觉神经元中的PAR-2参与疼痛信息的处理。因此,PAR-2参与多种生理和病理生理功能。PAR-2现在被认为是药物开发最重要的靶点分子之一。