心室离子通道与心律失常:生理学、病理生理学和药理学综述。

Medical review (Berlin, Germany) Pub Date : 2025-03-03 eCollection Date: 2025-06-01 DOI:10.1515/mr-2024-0085
Shiqi Liu, Wei Wang, Yang Yang, Zhuo Huang
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引用次数: 0

摘要

心脏离子通道是重要的跨膜蛋白,介导心脏功能的几乎所有方面,包括心脏动作电位(AP)的产生和传播以及心脏正常兴奋性和收缩的维持。此外,心脏离子通道在心脏健康和疾病中的关键作用被其功能失调突变对各种心律失常的深刻影响所强调。因此,离子通道是抗心律失常药物的重要靶点。本文首先综述了各种心脏离子通道的特点、结构及其在心脏电生理中的具体作用。随后,我们强调破坏离子通道功能的基因突变的影响,这与遗传性心律失常有关。最后,根据不同的治疗靶点,分别介绍了作用于心脏离子通道的抗心律失常药物。总之,本文旨在综述最突出的心室NaV、CaV、KV和Kir离子通道的生理学、病理生理学和药理学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ventricular ion channels and arrhythmias: an overview of physiology, pathophysiology and pharmacology.

Cardiac ion channels are critical transmembrane proteins that mediate almost all aspects of cardiac function including generation and propagation of cardiac action potential (AP) as well as maintenance of normal heart excitability and contraction. In addition, the pivotal role of cardiac ion channels in cardiac health and disease is underscored by the profound effects of their dysfunctional mutations on various arrhythmias. Hence, ion channels are vital targets for antiarrhythmic drugs. In this review, we first summarize the characteristics, structure of the various cardiac ion channels and their specific roles in cardiac electrophysiology. Subsequently, we highlight the implications of genetic mutations that disrupt ion channel function, which are associated with inherited cardiac arrhythmias. Finally, we address antiarrhythmic drugs acting on cardiac ion channels respectively, according to their therapeutic targets. In conclusion, this manuscript aims to review the physiology, pathophysiology and pharmacology of the most prominent ventricular NaV, CaV, KV, and Kir ion channels.

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