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电压和钙动力学均为心肌细胞电交替的基础。

Voltage and calcium dynamics both underlie cellular alternans in cardiac myocytes.

机构信息

Greenberg Division of Cardiology, Weill Cornell Medical College, New York, New York.

Greenberg Division of Cardiology, Weill Cornell Medical College, New York, New York; Department of Physiology and Biophysics, Weill Cornell Medical College, New York, New York.

出版信息

Biophys J. 2014 May 20;106(10):2222-32. doi: 10.1016/j.bpj.2014.03.048.

Abstract

Cardiac alternans, a putative trigger event for cardiac reentry, is a beat-to-beat alternation in membrane potential and calcium transient. Alternans was originally attributed to instabilities in transmembrane ion channel dynamics (i.e., the voltage mechanism). As of this writing, the predominant view is that instabilities in subcellular calcium handling are the main underlying mechanism. That being said, because the voltage and calcium systems are bidirectionally coupled, theoretical studies have suggested that both mechanisms can contribute. To date, to our knowledge, no experimental evidence of such a dual role within the same cell has been reported. Here, a combined electrophysiological and calcium imaging approach was developed and used to illuminate the contributions of voltage and calcium dynamics to alternans. An experimentally feasible protocol, quantification of subcellular calcium alternans and restitution slope during cycle-length ramping alternans control, was designed and validated. This approach allows simultaneous illumination of the contributions of voltage and calcium-driven instability to total cellular instability as a function of cycle-length. Application of this protocol in in vitro guinea-pig left-ventricular myocytes demonstrated that both voltage- and calcium-driven instabilities underlie alternans, and that the relative contributions of the two systems change as a function of pacing rate.

摘要

心脏交替,一种可能引发心脏折返的触发事件,是膜电位和钙瞬变的逐搏交替。交替最初归因于跨膜离子通道动力学的不稳定性(即电压机制)。截至目前,主要观点认为亚细胞钙处理的不稳定性是主要的潜在机制。话虽如此,由于电压和钙系统是双向耦合的,理论研究表明这两种机制都可能起作用。迄今为止,据我们所知,尚未有实验证据表明同一细胞中存在这种双重作用。在这里,开发了一种结合电生理和钙成像的方法,用于阐明电压和钙动力学对交替的贡献。设计并验证了一种在实验上可行的方案,用于在周期长度递增的交替控制期间量化亚细胞钙交替和恢复斜率。该方法允许同时照亮电压和钙驱动不稳定性对总细胞不稳定性的贡献,作为周期长度的函数。该方案在体外豚鼠左心室心肌细胞中的应用表明,电压和钙驱动的不稳定性均导致交替,并且两个系统的相对贡献随起搏率的变化而变化。

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