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ε蛋白激酶C作为缺血性心脏病的潜在治疗靶点。

Epsilon protein kinase C as a potential therapeutic target for the ischemic heart.

作者信息

Inagaki Koichi, Churchill Eric, Mochly-Rosen Daria

机构信息

Department of Molecular Pharmacology, Stanford University School of Medicine, CCSR, Room 3145A, 269 Campus Drive Stanford, CA 94305-5174, United States.

出版信息

Cardiovasc Res. 2006 May 1;70(2):222-30. doi: 10.1016/j.cardiores.2006.02.015. Epub 2006 Feb 23.

Abstract

Ischemic heart disease is the leading cause of morbidity and mortality in the western world. Ischemic damage can occur by acute myocardial infarction, stable angina, cardiac stunning, and myocardial hibernation. In addition, 'scheduled' ischemic events, occurring during cardiac surgery, heart transplantation, and elective angioplasty, can also result in cardiac damage. Ischemic or pharmacological preconditioning can decrease the extent of damage to the myocardium. Although the mechanism of preconditioning-mediated cardioprotection is not fully understood, epsilonPKC has been implicated as a critical mediator of this process in animal studies. The use of isozyme-specific pharmacological tools has permitted a better elucidation of the upstream stimuli and the downstream transducers of epsilonPKC in the pathways leading to cardioprotection. While little is known about the role of epsilonPKC in these pathways in humans, animal studies suggest a potential therapeutic role of epsilonPKC. This review will focus on the role of epsilonPKC in cardiac protection and on the signal transduction cascades that have been implicated in this protection.

摘要

缺血性心脏病是西方世界发病和死亡的主要原因。缺血性损伤可由急性心肌梗死、稳定型心绞痛、心脏顿抑和心肌冬眠引起。此外,在心脏手术、心脏移植和择期血管成形术期间发生的“计划性”缺血事件也可导致心脏损伤。缺血预处理或药物预处理可减少心肌损伤的程度。尽管预处理介导的心脏保护机制尚未完全明确,但在动物研究中,ε蛋白激酶C(epsilonPKC)被认为是这一过程的关键介质。使用同工酶特异性药理学工具能够更好地阐明导致心脏保护的信号通路中epsilonPKC的上游刺激因素和下游转导因子。虽然人们对epsilonPKC在人类这些信号通路中的作用知之甚少,但动物研究表明epsilonPKC具有潜在的治疗作用。本综述将聚焦于epsilonPKC在心脏保护中的作用以及与此保护相关的信号转导级联反应。

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