Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Department of Pharmacology, The University of Oxford, Oxford, UK.
Br J Pharmacol. 2018 Apr;175(8):1362-1374. doi: 10.1111/bph.13872. Epub 2017 Jun 28.
p21-activated kinase 1 (Pak1) is a member of the highly conserved family of serine/threonine protein kinases regulated by Ras-related small G-proteins, Cdc42/Rac1. It has been previously demonstrated to be involved in cardiac protection. Based on recent studies, this review provides an overview of the role of Pak1 in cardiac diseases including disrupted Ca homoeostasis-related cardiac arrhythmias, adrenergic stress- and pressure overload-induced hypertrophy, and ischaemia/reperfusion injury. These findings demonstrate the important role of Pak1 mediated through the phosphorylation and transcriptional modification of hypertrophy and/or arrhythmia-related genes. This review also discusses the anti-arrhythmic and anti-hypertrophic, protective function of Pak1 and the beneficial effects of fingolimod (an FDA-approved sphingolipid drug), a Pak1 activator, and its ability to prevent arrhythmias and cardiac hypertrophy. These findings also highlight the therapeutic potential of Pak1 signalling in the treatment and prevention of cardiac diseases.
This article is part of a themed section on Spotlight on Small Molecules in Cardiovascular Diseases. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.8/issuetoc.
p21 激活激酶 1(Pak1)是 Ras 相关小 G 蛋白调节的高度保守丝氨酸/苏氨酸蛋白激酶家族的成员,Cdc42/Rac1。先前已证明其参与心脏保护。基于最近的研究,本综述概述了 Pak1 在包括钙稳态紊乱相关心律失常、儿茶酚胺应激和压力超负荷诱导的肥大以及缺血/再灌注损伤在内的心脏疾病中的作用。这些发现表明 Pak1 通过磷酸化和转录修饰与肥大和/或心律失常相关基因的作用非常重要。本综述还讨论了 Pak1 的抗心律失常和抗肥大、保护作用,以及 fingolimod(一种获得 FDA 批准的鞘脂类药物)作为 Pak1 激活剂的有益作用,及其预防心律失常和心脏肥大的能力。这些发现还强调了 Pak1 信号在心脏疾病治疗和预防中的治疗潜力。
本文是心血管疾病小分子聚焦专题的一部分。要查看该部分中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.8/issuetoc.