Department of Medicine (Cardiology), David Geffen School of Medicine at University of California, Los Angeles, California, USA.
Biophys J. 2010 Aug 4;99(3):765-73. doi: 10.1016/j.bpj.2010.05.019.
Irregularly occurring early afterdepolarizations (EADs) in cardiac myocytes are traditionally hypothesized to be caused by random ion channel fluctuations. In this study, we combined 1), patch-clamp experiments in which action potentials were recorded at different pacing cycle lengths from isolated rabbit ventricular myocytes under several experimental conditions inducing EADs, including oxidative stress with hydrogen peroxide, calcium overload with BayK8644, and ionic stress with hypokalemia; 2), computer simulations using a physiologically detailed rabbit ventricular action potential model, in which repolarization reserve was reduced to generate EADs and random ion channel or path cycle length fluctuations were implemented; and 3), iterated maps with or without noise. By comparing experimental, modeling, and bifurcation analyses, we present evidence that noise-induced transitions between bistable states (i.e., between an action potential with and without an EAD) is not sufficient to account for the large variation in action potential duration fluctuations observed in experimental studies. We conclude that the irregular dynamics of EADs is intrinsically chaotic, with random fluctuations playing a nonessential, auxiliary role potentiating the complex dynamics.
心肌细胞中不规则早后除极(EAD)的传统假设是由随机离子通道波动引起的。在这项研究中,我们将 1)在不同起搏周期长度下从分离的兔心室肌细胞记录动作电位的膜片钳实验,包括在几种诱导 EAD 的实验条件下,如氧化应激与过氧化氢、钙超载与 BayK8644 以及低钾血症与离子应激;2)使用生理详细的兔心室动作电位模型的计算机模拟,其中复极储备减少以产生 EAD 并实施随机离子通道或路径周期长度波动;以及 3)具有或不具有噪声的迭代映射。通过比较实验、建模和分岔分析,我们提供了证据表明,噪声诱导的双稳态状态之间的转变(即,具有和不具有 EAD 的动作电位之间)不足以解释实验研究中观察到的动作电位持续时间波动的巨大变化。我们得出结论,EAD 的不规则动力学本质上是混沌的,随机波动起着非必要的辅助作用,增强了复杂的动力学。