心脏离子通道和心肌细胞电生理模型的新方法。

IF 2.9 Q2 BIOPHYSICS
Biophysics reviews Pub Date : 2023-03-01 Epub Date: 2023-03-30 DOI:10.1063/5.0127713
Jonathan D Moreno, Jonathan R Silva
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引用次数: 0

摘要

在心脏电生理学领域,建模几十年来一直发挥着核心作用。然而,尽管这项工作已经建立起来,但它最近看到了正在创建的模型的复杂性和预测能力的快速和持续的演变。特别是,新的建模方法允许跟踪平行和相互连接的过程,从确定离子通道门控的纳米和飞秒到描述心律失常所需的厘米和分钟。尺度之间的联系为心律失常的机制和药物治疗带来了前所未有的见解。这篇综述的重点是从第一性原理生成这些模型,生成描述离子通道动力学的详细模型,创建和数值求解动力学模型的算法,以及参数化这些模型的数据收集新方法。虽然我们关注的是这些模型在心律失常中的应用,但这些概念广泛适用于任何可兴奋细胞的生理和病理生理模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging methods to model cardiac ion channel and myocyte electrophysiology.

In the field of cardiac electrophysiology, modeling has played a central role for many decades. However, even though the effort is well-established, it has recently seen a rapid and sustained evolution in the complexity and predictive power of the models being created. In particular, new approaches to modeling have allowed the tracking of parallel and interconnected processes that span from the nanometers and femtoseconds that determine ion channel gating to the centimeters and minutes needed to describe an arrhythmia. The connection between scales has brought unprecedented insight into cardiac arrhythmia mechanisms and drug therapies. This review focuses on the generation of these models from first principles, generation of detailed models to describe ion channel kinetics, algorithms to create and numerically solve kinetic models, and new approaches toward data gathering that parameterize these models. While we focus on application of these models for cardiac arrhythmia, these concepts are widely applicable to model the physiology and pathophysiology of any excitable cell.

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CiteScore
3.60
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