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SCN5A与窦房结起搏功能。

SCN5A and sinoatrial node pacemaker function.

作者信息

Lei Ming, Zhang Henggui, Grace Andrew A, Huang Christopher L-H

机构信息

Cardiovascular Group, School of Medicine, The University of Manchester, Manchester, M13, 9NT, UK.

出版信息

Cardiovasc Res. 2007 Jun 1;74(3):356-65. doi: 10.1016/j.cardiores.2007.01.009. Epub 2007 Jan 19.

Abstract

The SCN5A gene encodes specific voltage-dependent Na+ channels abundant in cardiac muscle that open and close at specific stages of cardiac activity in response to voltage change, thereby controlling the magnitude and timecourse of voltage-dependent Na+ currents (iNa) in cardiac muscle cells. Although iNa has been recorded from sinoatrial (SA) node pacemaker cells, its precise role in SA node pacemaker function remains uncertain. This review summarizes recent findings bearing upon: (i) Sinus node dysfunction resulting from genetic mutations in SCN5A; (ii) Sinus node function in the murine cardiac model with targeted disruptions of the SCN5A gene; (iii) Experimental and computational evaluations of the functional roles of iNa in SA node pacemaker function. Taken together, these new observations suggest strong correlations between SCN5A-encoded Na+ channel and SA node pacemaker function.

摘要

SCN5A基因编码在心肌中大量存在的特定电压依赖性钠通道,这些通道在心脏活动的特定阶段响应电压变化而打开和关闭,从而控制心肌细胞中电压依赖性钠电流(iNa)的大小和时程。尽管已经从窦房(SA)结起搏细胞中记录到iNa,但其在SA结起搏功能中的精确作用仍不确定。本综述总结了近期关于以下方面的研究结果:(i)SCN5A基因突变导致的窦房结功能障碍;(ii)SCN5A基因靶向破坏的小鼠心脏模型中的窦房结功能;(iii)iNa在SA结起搏功能中的功能作用的实验和计算评估。综合来看,这些新观察结果表明SCN5A编码的钠通道与SA结起搏功能之间存在密切关联。

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