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Exploiting mathematical models to illuminate electrophysiological variability between individuals

机译:利用数学模型阐明个体之间的电生理变异性

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Across individuals within a population, several levels of variability are observed, from the differential expression of ion channels at the molecular level, to the various action potential morphologies observed at the cellular level, to divergent responses to drugs at the organismal level. However, the limited ability of experiments to probe complex interactions between components has hitherto hindered our understanding of the factors that cause a range of behaviours within a population. Variability is a challenging issue that is encountered in all physiological disciplines, but recent work suggests that novel methods for analysing mathematical models can assist in illuminating its causes. In this review, we discuss mathematical modelling studies in cardiac electrophysiology and neuroscience that have enhanced our understanding of variability in a number of key areas. Specifically, we discuss parameter sensitivity analysis techniques that may be applied to generate quantitative predictions based on considering behaviours within a population of models, thereby providing novel insight into variability. Our discussion focuses on four issues that have benefited from the utilization of these methods: (1) the comparison of different electrophysiological models of cardiac myocytes, (2) the determination of the individual contributions of different molecular changes in complex disease phenotypes, (3) the identification of the factors responsible for the variable response to drugs, and (4) the constraining of free parameters in electrophysiological models of heart cells. Together, the studies that we discuss suggest that rigorous analyses of mathematical models can generate quantitative predictions regarding how molecular-level variations contribute to functional differences between experimental samples. These strategies may be applicable not just in cardiac electrophysiology, but in a wide range of disciplines.
机译:在种群中的各个个体之间,观察到了几个水平的可变性,从分子水平上离子通道的差异表达到细胞水平上观察到的各种动作电位形态,再到生物水平上对药物的不同反应。然而,迄今为止,实验探测组分之间复杂相互作用的能力有限,这阻碍了我们对引起种群内一系列行为的因素的理解。可变性是所有生理学科都遇到的具有挑战性的问题,但是最近的工作表明,用于分析数学模型的新颖方法可以帮助阐明其原因。在这篇综述中,我们讨论了心脏电生理学和神经科学中的数学建模研究,这些研究增强了我们对许多关键领域中变异性的理解。具体来说,我们讨论了参数敏感性分析技术,该技术可用于考虑模型群体内的行为来生成定量预测,从而提供对可变性的新颖见解。我们的讨论集中在受益于这些方法的使用的四个问题上:(1)心肌细胞不同电生理模型的比较;(2)确定复杂疾病表型中不同分子变化的个体贡献;(3)确定负责药物反应的因素,以及(4)限制心脏细胞电生理模型中的自由参数。总之,我们讨论的研究表明,对数学模型进行严格的分析可以生成有关分子水平变化如何导致实验样品之间功能差异的定量预测。这些策略可能不仅适用于心脏电生理学,而且适用于广泛的学科。

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