Diekman Casey O, Wei Ning
Department of Mathematical Sciences, New Jersey Institute of Technology, Newark, New Jersey; EPSRC Centre for Predictive Modelling in Healthcare, Living Systems Institute, University of Exeter, Exeter, United Kingdom.
Department of Mathematics, Purdue University, West Lafayette, Indiana.
Biophys J. 2021 Jan 19;120(2):319-333. doi: 10.1016/j.bpj.2020.11.2264. Epub 2020 Dec 5.
Sudden cardiac arrest is a malfunction of the heart's electrical system, typically caused by ventricular arrhythmias, that can lead to sudden cardiac death (SCD) within minutes. Epidemiological studies have shown that SCD and ventricular arrhythmias are more likely to occur in the morning than in the evening, and laboratory studies indicate that these daily rhythms in adverse cardiovascular events are at least partially under the control of the endogenous circadian timekeeping system. However, the biophysical mechanisms linking molecular circadian clocks to cardiac arrhythmogenesis are not fully understood. Recent experiments have shown that L-type calcium channels exhibit circadian rhythms in both expression and function in guinea pig ventricular cardiomyocytes. We developed an electrophysiological model of these cells to simulate the effect of circadian variation in L-type calcium conductance. In our simulations, we found that there is a circadian pattern in the occurrence of early afterdepolarizations (EADs), which are abnormal depolarizations during the repolarization phase of a cardiac action potential that can trigger fatal ventricular arrhythmias. Specifically, the model produces EADs in the morning, but not at other times of day. We show that the model exhibits a codimension-2 Takens-Bogdanov bifurcation that serves as an organizing center for different types of EAD dynamics. We also simulated a two-dimensional spatial version of this model across a circadian cycle. We found that there is a circadian pattern in the breakup of spiral waves, which represents ventricular fibrillation in cardiac tissue. Specifically, the model produces spiral wave breakup in the morning, but not in the evening. Our computational study is the first, to our knowledge, to propose a link between circadian rhythms and EAD formation and suggests that the efficacy of drugs targeting EAD-mediated arrhythmias may depend on the time of day that they are administered.
心脏骤停是心脏电系统的故障,通常由室性心律失常引起,可在数分钟内导致心源性猝死(SCD)。流行病学研究表明,SCD和室性心律失常在早晨比在晚上更易发生,实验室研究表明,这些不良心血管事件的每日节律至少部分受内源性昼夜节律计时系统的控制。然而,将分子生物钟与心律失常发生联系起来的生物物理机制尚未完全明确。最近的实验表明,L型钙通道在豚鼠心室心肌细胞中的表达和功能均呈现昼夜节律。我们建立了这些细胞的电生理模型,以模拟L型钙电导昼夜变化的影响。在我们的模拟中,我们发现早期后去极化(EADs)的发生存在昼夜模式,EADs是心脏动作电位复极化阶段的异常去极化,可引发致命的室性心律失常。具体而言,该模型在早晨产生EADs,而在一天中的其他时间则不会。我们表明,该模型表现出一个余维2的Takens-Bogdanov分岔,它作为不同类型EAD动力学的组织中心。我们还在一个昼夜周期内模拟了该模型的二维空间版本。我们发现螺旋波破裂存在昼夜模式,螺旋波破裂代表心脏组织中的心室颤动。具体而言,该模型在早晨产生螺旋波破裂,而在晚上则不会。据我们所知,我们的计算研究首次提出了昼夜节律与EAD形成之间的联系,并表明针对EAD介导的心律失常的药物疗效可能取决于给药的时间。