Mechanical Engineering Department, University College London, Torrington Place, London, UK.
Comput Biol Med. 2012 Oct;42(10):982-92. doi: 10.1016/j.compbiomed.2012.07.010. Epub 2012 Aug 24.
In cardiovascular computational physiology the importance of understanding cardiac contraction as a multi-scale process is of paramount importance to understand causality across different scales. Within this study, a multi-scale and multi-physics model of the left ventricle that connects the process of cardiac excitation and contraction from the protein to the organ level is presented in a novel way. The model presented here includes the functional description of a cardiomyocyte (cellular scale), which explains the dynamic behaviour of the calcium concentration within the cell whilst an action potential develops. The cell domain is coupled to a domain that determines the kinetics of the sliding filament mechanism (protein level), which is at the basis of cardiac contraction. These processes are then linked to the generation of muscular force and from there to the generation of pressure inside the ventricle. This multi-scale model presents a coherent and unified way to describe cardiac contraction from the protein to the organ level.
在心血管计算生理学中,理解心脏收缩作为一个多尺度过程至关重要,这对于理解不同尺度之间的因果关系至关重要。在本研究中,以新颖的方式提出了一种连接从蛋白质到器官水平的心脏兴奋和收缩过程的左心室多尺度多物理模型。这里提出的模型包括心肌细胞(细胞尺度)的功能描述,它解释了动作电位发展过程中细胞内钙浓度的动态行为。细胞域与确定滑动丝机制动力学的域(蛋白质水平)耦合,滑动丝机制是心脏收缩的基础。然后,这些过程与肌肉力的产生相关联,并且从那里与心室内部压力的产生相关联。这种多尺度模型提供了一种连贯而统一的方法来描述从蛋白质到器官水平的心脏收缩。