Oka M, Fagan K A, Jones P L, McMurtry I F
Department of Pharmacology and Center for Lung Biology, University of South Alabama, College of Medicine, Mobile, AL 36688, USA.
Br J Pharmacol. 2008 Oct;155(4):444-54. doi: 10.1038/bjp.2008.239. Epub 2008 Jun 9.
A burgeoning body of evidence suggests that RhoA/Rho kinase (ROCK) signalling plays an important role in the pathogenesis of various experimental models of pulmonary hypertension (PH), including chronic hypoxia-, monocrotaline-, bleomycin-, shunt- and vascular endothelial growth factor receptor inhibition plus chronic hypoxia-induced PH. ROCK has been incriminated in pathophysiologic events ranging from mediation of sustained abnormal vasoconstriction to promotion of vascular inflammation and remodelling. In addition, the 3-hydroxy-3-methylglutaryl CoA reductase inhibitors, statins, which inhibit activation of RhoA by preventing post-translational isoprenylation of the protein and its translocation to the plasma membrane ameliorate PH in several different rat models, and may also be effective in PH patients. Also, phosphorylation of RhoA and prevention of its translocation to the plasma membrane are involved in the protective effect of the type 5-PDE inhibitor, sildenafil, against hypoxia- and bleomycin-induced PH. Collectively, these and other observations indicate that independent of the cause of PH, activation of the RhoA/ROCK pathway serves as a point of convergence of various signalling cascades in the pathogenesis of the disease. We propose that ROCK inhibitors and other drugs that inhibit this pathway might be useful in the treatment of various forms of PH.
越来越多的证据表明,RhoA/ Rho激酶(ROCK)信号通路在各种肺动脉高压(PH)实验模型的发病机制中起重要作用,这些模型包括慢性低氧、野百合碱、博来霉素、分流以及血管内皮生长因子受体抑制加慢性低氧诱导的PH。ROCK参与了从介导持续性异常血管收缩到促进血管炎症和重塑等一系列病理生理过程。此外,3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)通过阻止蛋白质的翻译后异戊二烯化及其向质膜的转位来抑制RhoA的激活,在几种不同的大鼠模型中可改善PH,对PH患者可能也有效。而且,RhoA的磷酸化及其向质膜转位的抑制参与了5型磷酸二酯酶抑制剂西地那非对低氧和博来霉素诱导的PH的保护作用。总的来说,这些及其他观察结果表明,无论PH的病因如何,RhoA/ROCK通路的激活在该疾病的发病机制中是各种信号级联反应的汇聚点。我们认为ROCK抑制剂和其他抑制该通路的药物可能对治疗各种形式的PH有用。