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钙信号与心律失常

Calcium Signaling and Cardiac Arrhythmias.

作者信息

Landstrom Andrew P, Dobrev Dobromir, Wehrens Xander H T

机构信息

From the Section of Cardiology, Department of Pediatrics (A.P.L.), Cardiovascular Research Institute (A.P.L., X.H.T.W.), and Departments of Molecular Physiology and Biophysics, Medicine (Cardiology), Center for Space Medicine (X.H.T.W.), Baylor College of Medicine, Houston, TX; and Institute of Pharmacology, West German Heart and Vascular Center, University Duisburg-Essen, Essen, Germany (D.D.).

出版信息

Circ Res. 2017 Jun 9;120(12):1969-1993. doi: 10.1161/CIRCRESAHA.117.310083.

Abstract

There has been a significant progress in our understanding of the molecular mechanisms by which calcium (Ca) ions mediate various types of cardiac arrhythmias. A growing list of inherited gene defects can cause potentially lethal cardiac arrhythmia syndromes, including catecholaminergic polymorphic ventricular tachycardia, congenital long QT syndrome, and hypertrophic cardiomyopathy. In addition, acquired deficits of multiple Ca-handling proteins can contribute to the pathogenesis of arrhythmias in patients with various types of heart disease. In this review article, we will first review the key role of Ca in normal cardiac function-in particular, excitation-contraction coupling and normal electric rhythms. The functional involvement of Ca in distinct arrhythmia mechanisms will be discussed, followed by various inherited arrhythmia syndromes caused by mutations in Ca-handling proteins. Finally, we will discuss how changes in the expression of regulation of Ca channels and transporters can cause acquired arrhythmias, and how these mechanisms might be targeted for therapeutic purposes.

摘要

我们对钙离子介导各种类型心律失常的分子机制的理解取得了重大进展。越来越多的遗传性基因缺陷可导致潜在致命的心律失常综合征,包括儿茶酚胺能多形性室性心动过速、先天性长QT综合征和肥厚型心肌病。此外,多种钙处理蛋白的后天性缺陷可促成各类心脏病患者心律失常的发病机制。在这篇综述文章中,我们将首先回顾钙在正常心脏功能中的关键作用——特别是兴奋-收缩偶联和正常电节律。将讨论钙在不同心律失常机制中的功能参与情况,随后探讨由钙处理蛋白突变引起的各种遗传性心律失常综合征。最后,我们将讨论钙通道和转运体的表达调控变化如何导致后天性心律失常,以及这些机制如何可能成为治疗靶点。

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