Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Am J Physiol Heart Circ Physiol. 2011 Aug;301(2):H287-96. doi: 10.1152/ajpheart.00327.2011. Epub 2011 May 27.
Rho-kinase (ROCKs) belongs to the family of serine/threonine kinases and is an important downstream effector of the small GTP-binding protein RhoA. There are two isoforms of Rho-kinase, ROCK1 and ROCK2, and they have different functions with ROCK1 for circulating inflammatory cells and ROCK2 for vascular smooth muscle cells. It has been demonstrated that the RhoA/Rho-kinase pathway plays an important role in various fundamental cellular functions, including contraction, motility, proliferation, and apoptosis, leading to the development of cardiovascular disease. The important role of Rho-kinase in vivo has been demonstrated in the pathogenesis of vasospasm, arteriosclerosis, ischemia-reperfusion injury, hypertension, pulmonary hypertension, stroke, and heart failure. Furthermore, the beneficial effects of fasudil, a selective Rho-kinase inhibitor, have been demonstrated for the treatment of several cardiovascular diseases in humans. Thus the Rho-kinase pathway is an important new therapeutic target in cardiovascular medicine.
Rho-kinase (ROCKs) 属于丝氨酸/苏氨酸激酶家族,是小 GTP 结合蛋白 RhoA 的重要下游效应物。Rho-kinase 有两种同工型,ROCK1 和 ROCK2,它们具有不同的功能,ROCK1 作用于循环炎症细胞,ROCK2 作用于血管平滑肌细胞。已经证明,RhoA/Rho-kinase 通路在各种基本细胞功能中发挥重要作用,包括收缩、运动、增殖和凋亡,导致心血管疾病的发生。在血管痉挛、动脉硬化、缺血再灌注损伤、高血压、肺动脉高压、中风和心力衰竭的发病机制中已经证明 Rho-kinase 在体内的重要作用。此外,Rho-kinase 的选择性抑制剂法舒地尔已被证明对人类几种心血管疾病具有治疗作用。因此,Rho-kinase 通路是心血管医学中的一个重要的新治疗靶点。