Centre for Mathematical Medicine and Biology, School of Mathematical Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Centre for Mathematical Medicine and Biology, School of Mathematical Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
J Theor Biol. 2019 Oct 7;478:102-114. doi: 10.1016/j.jtbi.2019.06.016. Epub 2019 Jun 17.
Cardiac alternans, in which the membrane potential and the intracellular calcium concentration exhibit alternating durations and peak amplitudes at consecutive beats, constitute a precursor to fatal cardiac arrhythmia such as sudden cardiac death. A crucial question therefore concerns the onset of cardiac alternans. Typically, alternans are only reported when they are fully developed. Here, we present a modelling approach to explore recently discovered microscopic alternans, which represent one of the earliest manifestations of cardiac alternans. In this case, the regular periodic dynamics of the local intracellular calcium concentration is already unstable, while the whole-cell behaviour suggests a healthy cell state. In particular, we use our model to investigate the impact of calcium diffusion in both the cytosol and the sarcoplasmic reticulum on the formation of microscopic calcium alternans. We find that for dominant cytosolic coupling, calcium alternans emerge via the traditional period doubling bifurcation. In contrast, dominant luminal coupling leads to a novel route to calcium alternans through a saddle-node bifurcation at the network level. Combining semi-analytical and computational approaches, we compute areas of stability in parameter space and find that as we cross from stable to unstable regions, the emergent patterns of the intracellular calcium concentration change abruptly in a fashion that is highly dependent upon position along the stability boundary. Our results demonstrate that microscopic calcium alternans may possess a much richer dynamical repertoire than previously thought and further strengthen the role of luminal calcium in shaping cardiac calcium dynamics.
心脏交替现象,即细胞膜电位和细胞内钙离子浓度在连续搏动时呈现出交替的持续时间和峰值幅度,是致命性心律失常(如心源性猝死)的前兆。因此,一个关键问题涉及到心脏交替现象的起始。通常情况下,只有当交替现象完全发展时才会报告。在这里,我们提出了一种建模方法来探索最近发现的微观交替现象,这是心脏交替现象的最早表现之一。在这种情况下,局部细胞内钙离子浓度的规则周期性动力学已经不稳定,而整个细胞的行为表明细胞处于健康状态。特别是,我们使用模型来研究细胞质和肌浆网中的钙离子扩散对微观钙离子交替现象形成的影响。我们发现,对于占主导地位的细胞质耦合,钙离子交替现象通过传统的倍周期分岔出现。相比之下,主导的腔室耦合导致通过网络级别的鞍结分岔出现钙离子交替现象的新途径。结合半解析和计算方法,我们计算了参数空间中的稳定性区域,并发现当我们从稳定区域过渡到不稳定区域时,细胞内钙离子的涌现模式会突然发生变化,这种变化高度依赖于沿着稳定性边界的位置。我们的结果表明,微观钙离子交替现象可能比之前认为的具有更丰富的动力学谱,并且进一步加强了腔室钙离子在塑造心脏钙离子动力学中的作用。