Pfeiffer Emily R, Tangney Jared R, Omens Jeffrey H, McCulloch Andrew D
J Biomech Eng. 2014 Feb;136(2):021007. doi: 10.1115/1.4026221.
Cardiac mechanical contraction is triggered by electrical activation via an intracellular calcium-dependent process known as excitation-contraction coupling. Dysregulation of cardiac myocyte intracellular calcium handling is a common feature of heart failure. At the organ scale, electrical dyssynchrony leads to mechanical alterations and exacerbates pump dysfunction in heart failure. A reverse coupling between cardiac mechanics and electrophysiology is also well established. It is commonly referred as cardiac mechanoelectric feedback and thought to be an important contributor to the increased risk of arrhythmia during pathological conditions that alter regional cardiac wall mechanics, including heart failure. At the cellular scale, most investigations of myocyte mechanoelectric feedback have focused on the roles of stretch-activated ion channels, though mechanisms that are independent of ionic currents have also been described. Here we review excitation-contraction coupling and mechanoelectric feedback at the cellular and organ scales, and we identify the need for new multicellular tissue-scale model systems and experiments that can help us to obtain a better understanding of how interactions between electrophysiological and mechanical processes at the cell scale affect ventricular electromechanical interactions at the organ scale in the normal and diseased heart.
心脏的机械收缩是由电激活通过一种称为兴奋 - 收缩偶联的细胞内钙依赖性过程触发的。心肌细胞内钙处理的失调是心力衰竭的一个常见特征。在器官层面,电不同步会导致机械改变,并加剧心力衰竭中的泵功能障碍。心脏力学与电生理学之间的反向偶联也已得到充分证实。它通常被称为心脏机械电反馈,并且被认为是在改变局部心脏壁力学的病理状态(包括心力衰竭)期间心律失常风险增加的一个重要因素。在细胞层面,大多数关于心肌细胞机械电反馈的研究都集中在牵张激活离子通道的作用上,不过也描述了一些独立于离子电流的机制。在这里,我们综述了细胞和器官层面的兴奋 - 收缩偶联以及机械电反馈,并且我们确定需要新的多细胞组织层面的模型系统和实验,这些能够帮助我们更好地理解在正常和患病心脏中,细胞层面的电生理过程与机械过程之间的相互作用如何影响器官层面的心室机电相互作用。