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心房电生理学的特点:更好地理解心脏功能和心律失常机制的线索。

Specificities of atrial electrophysiology: Clues to a better understanding of cardiac function and the mechanisms of arrhythmias.

机构信息

INSERM, UMRS-956, 75013 Paris, France.

出版信息

J Mol Cell Cardiol. 2010 Jan;48(1):90-5. doi: 10.1016/j.yjmcc.2009.08.029. Epub 2009 Sep 8.

DOI:10.1016/j.yjmcc.2009.08.029
PMID:19744488
Abstract

The electrical properties of the atria and ventricles differ in several aspects reflecting the distinct role of the atria in cardiac physiology. The study of atrial electrophysiology had greatly contributed to the understanding of the mechanisms of atrial fibrillation (AF). Only the atrial L-type calcium current is regulated by serotonine or, under basal condition, by phosphodiesterases. These distinct regulations can contribute to I(Ca) down-regulation observed during AF, which is an important determinant of action potential refractory period shortening. The voltage-gated potassium current, I(Kur), has a prominent role in the repolarization of the atrial but not ventricular AP. In many species, this current is based on the functional expression of K(V)1.5 channels, which might represent a specific therapeutic target for AF. Mechanisms regulating the trafficking of K(V)1.5 channels to the plasma membrane are being actively investigated. The resting potential of atrial myocytes is maintained by various inward rectifier currents which differ with ventricle currents by a reduced density of I(K1), the presence of a constitutively active I(KACh) and distinct regulation of I(KATP). Stretch-sensitive or mechanosensitive ion channels are particularly active in atrial myocytes and are involved in the secretion of the natriuretic peptide. Integration of knowledge on electrical properties of atrial myocytes in comprehensive schemas is now necessary for a better understanding of the physiology of atria and the mechanisms of AF.

摘要

心房和心室在几个方面的电特性不同,反映了心房在心脏生理学中的独特作用。心房电生理学的研究极大地促进了对心房颤动 (AF) 机制的理解。只有心房 L 型钙电流受血清素调节,或在基础条件下受磷酸二酯酶调节。这些不同的调节可以有助于在 AF 期间观察到的 I(Ca)下调,这是动作电位不应期缩短的重要决定因素。电压门控钾电流 I(Kur)在心房而不是心室 AP 的复极化中起重要作用。在许多物种中,这种电流基于 K(V)1.5 通道的功能表达,这可能是 AF 的特定治疗靶点。调节 K(V)1.5 通道向质膜易位的机制正在积极研究中。心房肌细胞的静息电位由各种内向整流电流维持,这些电流与心室电流的不同之处在于 I(K1)的密度降低、存在组成型激活的 I(KACh)和 I(KATP)的不同调节。伸展敏感或机械敏感离子通道在心房肌细胞中特别活跃,并参与利钠肽的分泌。整合心房肌细胞电特性的知识到综合图式中对于更好地理解心房生理学和 AF 机制是必要的。

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