Department of Computer Science, University of Oxford, Oxford, UK.
J Physiol. 2012 Sep 15;590(18):4553-69. doi: 10.1113/jphysiol.2012.231928. Epub 2012 May 21.
To investigate the effects of the coupling between excitation and contraction on whole-organ function, we have developed a novel biophysically based multiscale electromechanical model of the murine heart. Through comparison with a comprehensive in vivo experimental data set, we show good agreement with pressure and volume measurements at both physiological temperatures and physiological pacing frequencies. This whole-organ model was used to investigate the effects of material and haemodynamic properties introduced at the tissue level, as well as emergent function of our novel cell contraction model. Through a comprehensive sensitivity analysis at both the cellular and whole organ level, we demonstrate the sensitivity of the model's results to its parameters and the constraining effect of experimental data. These results demonstrate the fundamental importance of length- and velocity-dependent feedback to the cellular scale for whole-organ function, and we show that a strong velocity dependence of tension is essential for explaining the differences between measured single cell tension and whole-organ pressure transients.
为了研究兴奋和收缩之间的耦合对整体器官功能的影响,我们开发了一种新的基于生物物理的鼠心多尺度机电模型。通过与综合的体内实验数据集进行比较,我们在生理温度和生理起搏频率下显示出与压力和体积测量的良好一致性。这个整体器官模型被用来研究组织水平上引入的材料和血液动力学特性以及我们新的细胞收缩模型的涌现功能的影响。通过在细胞和整体器官水平上进行全面的敏感性分析,我们证明了模型结果对其参数的敏感性以及实验数据的约束作用。这些结果表明,长度和速度依赖性反馈对整体器官功能的细胞尺度至关重要,我们表明,张力的强烈速度依赖性对于解释测量的单个细胞张力和整体器官压力瞬变之间的差异是必不可少的。