Professor H. Zhang: School of Physics and Astronomy, The University of Manchester, Manchester M13 9PL, UK.
J Physiol. 2013 Sep 1;591(17):4249-72. doi: 10.1113/jphysiol.2013.254987. Epub 2013 Jun 3.
Chronic atrial fibrillation (AF) is associated with structural and electrical remodelling in the atria, which are associated with a high recurrence of AF. Through biophysically detailed computer modelling, this study investigated mechanisms by which AF-induced electrical remodelling promotes and perpetuates AF. A family of Courtemanche-Ramirez-Nattel variant models of human atrial cell action potentials (APs), taking into account of intrinsic atrial electrophysiological properties, was modified to incorporate various experimental data sets on AF-induced changes of major ionic channel currents (ICaL, IKur, Ito, IK1, IKs, INaCa) and on intracellular Ca(2+) handling. The single cell models for control and AF-remodelled conditions were incorporated into multicellular three-dimensional (3D) atrial tissue models. Effects of the AF-induced electrical remodelling were quantified as the changes of AP profile, AP duration (APD) and its dispersion across the atria, and the vulnerability of atrial tissue to the initiation of re-entry. The dynamic behaviour of re-entrant excitation waves in the 3D models was characterised. In our simulations, AF-induced electrical remodelling abbreviated atrial APD non-uniformly across the atria; this resulted in relatively short APDs co-existing with marked regional differences in the APD at junctions of the crista terminalis/pectinate muscle, pulmonary veins/left atrium. As a result, the measured tissue vulnerability to re-entry initiation at these tissue junctions was increased. The AF-induced electrical remodelling also stabilized and accelerated re-entrant excitation waves, leading to rapid and sustained re-entry. Under the AF-remodelled condition, re-entrant scroll waves in the 3D model degenerated into persistent and erratic wavelets, leading to fibrillation. In conclusion, realistic 3D atrial tissue models indicate that AF-induced electrical remodelling produces regionally heterogeneous and shortened APD; these respectively facilitate initiation and maintenance of re-entrant excitation waves.
慢性心房颤动(AF)与心房的结构和电重构有关,这与 AF 的高复发率有关。通过生物物理详细的计算机建模,本研究探讨了 AF 诱导的电重构促进和维持 AF 的机制。一组考虑到内在心房电生理特性的 Courtemanche-Ramirez-Nattel 变体人类心房细胞动作电位(AP)模型,被修改为纳入关于 AF 诱导的主要离子通道电流(ICaL、IKur、Ito、IK1、IKs、INaCa)和细胞内 Ca(2+)处理的变化的各种实验数据集。对照和 AF 重构条件的单细胞模型被纳入三维(3D)心房组织模型。作为 AF 诱导的电重构的效应,通过 AP 轮廓、APD(APD)及其在心房中的弥散以及心房组织对折返起始的易感性的变化来量化。3D 模型中折返兴奋波的动态行为特征。在我们的模拟中,AF 诱导的电重构使心房 APD 在心房内不均匀缩短;这导致相对较短的 APD 与在冠状静脉终嵴/梳状肌、肺静脉/左心房交界处的 APD 存在明显的区域差异并存。因此,在这些组织交界处,组织对折返起始的易感性增加。AF 诱导的电重构还稳定并加速折返兴奋波,导致快速和持续的折返。在 AF 重构条件下,3D 模型中的折返卷曲波退化为持续和不稳定的波,导致颤动。总之,现实的 3D 心房组织模型表明,AF 诱导的电重构产生区域异质性和缩短的 APD;这些分别促进折返兴奋波的起始和维持。