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心脏兰尼碱受体在心力衰竭和心源性猝死中的作用。

Roles of cardiac ryanodine receptor in heart failure and sudden cardiac death.

作者信息

Phrommintikul Arintaya, Chattipakorn Nipon

机构信息

Department of Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Int J Cardiol. 2006 Sep 20;112(2):142-52. doi: 10.1016/j.ijcard.2005.11.106. Epub 2006 May 15.

Abstract

Calcium (Ca2+) plays an important role as a messenger in the excitation-contraction coupling process of the myocardium. It is stored in the sarcoplasmic reticulum (SR) and released via a calcium release channel called the ryanodine receptor. Cardiac ryanodine receptor (RyR2) controls Ca2+ release, which is essential for cardiac contractility. There are several molecules which bind and regulate the function of RyR2 including calstabin2, calmodulin, protein kinase A (PKA), phosphatase, sorcin and calsequestrin. Alteration of RyR2 and associated molecules can cause functional and/or structural changes of the heart, leading to heart failure and sudden cardiac death. In this review, the alteration of RyR2 and its regulatory proteins, and its roles in heart failure and sudden cardiac death, are discussed. Evidence of a possible novel therapy targeting RyR2 and its associated regulatory proteins, currently proposed by investigators, is also included in this article.

摘要

钙(Ca2+)作为一种信使,在心肌兴奋-收缩偶联过程中发挥着重要作用。它储存于肌浆网(SR)中,并通过一种名为兰尼碱受体的钙释放通道释放。心脏兰尼碱受体(RyR2)控制Ca2+的释放,这对心脏收缩力至关重要。有几种分子可与RyR2结合并调节其功能,包括钙调蛋白2、钙调蛋白、蛋白激酶A(PKA)、磷酸酶、亲环蛋白和肌集钙蛋白。RyR2及其相关分子的改变可导致心脏功能和/或结构变化,进而导致心力衰竭和心源性猝死。在本综述中,将讨论RyR2及其调节蛋白的改变,以及它们在心力衰竭和心源性猝死中的作用。本文还纳入了研究人员目前提出的针对RyR2及其相关调节蛋白的一种可能新疗法的证据。

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