Qu Zhilin, Liu Michael B, Nivala Michael
Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, California, 90095, USA.
Department of Biomathematics, David Geffen School of Medicine, University of California, Los Angeles, California, 90095, USA.
Sci Rep. 2016 Oct 20;6:35625. doi: 10.1038/srep35625.
Intracellular calcium (Ca) alternans is a dynamical phenomenon in ventricular myocytes, which is linked to the genesis of lethal arrhythmias. Iterated map models of intracellular Ca cycling dynamics in ventricular myocytes under periodic pacing have been developed to study the mechanisms of Ca alternans. Two mechanisms of Ca alternans have been demonstrated in these models: one relies mainly on fractional sarcoplasmic reticulum Ca release and uptake, and the other on refractoriness and other properties of Ca sparks. Each of the two mechanisms can partially explain the experimental observations, but both have their inconsistencies with the experimental results. Here we developed an iterated map model that is composed of two coupled iterated maps, which unifies the two mechanisms into a single cohesive mathematical framework. The unified theory can consistently explain the seemingly contradictory experimental observations and shows that the two mechanisms work synergistically to promote Ca alternans. Predictions of the theory were examined in a physiologically-detailed spatial Ca cycling model of ventricular myocytes.
细胞内钙(Ca)交替变化是心室肌细胞中的一种动态现象,与致死性心律失常的发生有关。为了研究钙交替变化的机制,已经建立了周期性起搏下心室肌细胞内钙循环动力学的迭代映射模型。在这些模型中已经证明了钙交替变化的两种机制:一种主要依赖于肌浆网钙释放和摄取的分数,另一种依赖于钙火花的不应期和其他特性。这两种机制中的每一种都可以部分解释实验观察结果,但两者都与实验结果存在不一致之处。在这里,我们开发了一个由两个耦合迭代映射组成的迭代映射模型,将这两种机制统一到一个连贯的数学框架中。该统一理论可以一致地解释看似矛盾的实验观察结果,并表明这两种机制协同作用以促进钙交替变化。该理论的预测在心室肌细胞的生理详细空间钙循环模型中进行了检验。