Shin Hwa Kyoung, Salomone Salvatore, Ayata Cenk
Pusan National University, Medical Research Center for Ischemic Tissue Regeneration, 10 Ami-dong, 1-Ga, Seo-Gu, Busan 602-739, Korea.
Expert Opin Ther Targets. 2008 Dec;12(12):1547-64. doi: 10.1517/14728220802539244.
Rho and Rho-associated kinase (ROCK) play pivotal roles in pathogenesis of vascular diseases including stroke. ROCK is expressed in all cell types relevant to stroke, and regulates a range of physiological processes.
To provide an overview of ROCK as an experimental therapeutic target in cerebral ischemia, and the translational opportunities and obstacles in the prophylaxis and treatment of stroke.
Relevant literature was reviewed.
ROCK activity is upregulated in chronic vascular risk factors such as diabetes, hyperlipidemia and hypertension, and more acutely by cerebral ischemia. ROCK activation is predicted to increase the risk of cerebral ischemia, and worsen the ischemic tissue outcome and functional recovery. Evidence suggests that ROCK inhibition is protective in models of cerebral ischemia. The benefit is mediated through multiple mechanisms.
ROCK is a promising therapeutic target in all stages of stroke.
Rho 及 Rho 相关激酶(ROCK)在包括中风在内的血管疾病发病机制中起关键作用。ROCK 在与中风相关的所有细胞类型中均有表达,并调节一系列生理过程。
综述 ROCK 作为脑缺血实验性治疗靶点的研究概况,以及在中风预防和治疗方面的转化机遇与障碍。
查阅相关文献。
在糖尿病、高脂血症和高血压等慢性血管危险因素中,ROCK 活性上调,而脑缺血会使其更迅速地上调。预计 ROCK 激活会增加脑缺血风险,并使缺血组织结局和功能恢复恶化。有证据表明,在脑缺血模型中抑制 ROCK 具有保护作用。这种益处是通过多种机制介导的。
ROCK 是中风各阶段有前景的治疗靶点。