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首页> 外文期刊>The Journal of Physiology >Pro-arrhythmogenic effects of atrial fibrillation-induced electrical remodelling: Insights from the three-dimensional virtual human atria
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Pro-arrhythmogenic effects of atrial fibrillation-induced electrical remodelling: Insights from the three-dimensional virtual human atria

机译:心房颤动引起的电重构的促心律失常作用:三维虚拟人心房的见解

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摘要

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 Ca2+ 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.
机译:慢性心房纤颤(AF)与心房的结构和电重构有关,与房颤的高复发有关。通过生物物理上详细的计算机建模,本研究调查了房颤诱发的电重构促进和维持房颤的机制。考虑到固有的心房电生理特性,对人心房细胞动作电位(AP)的Courtemanche-Ramirez-Nattel变体模型家族进行了修改,以纳入关于AF诱导的主要离子通道电流(ICaL, IKur,伊藤,IK1,IK,INaCa)以及细胞内Ca2 +处理。将用于对照和AF重塑条件的单细胞模型整合到多细胞三维(3D)心房组织模型中。 AF引起的电重构的影响可量化为AP轮廓,AP持续时间(APD)及其在心房中的分散以及心房组织对再次进入的脆弱性的变化。表征了3D模型中折返激励波的动态行为。在我们的模拟中,AF引起的电重构在整个心房中缩写为APD。这导致相对较短的APD并存,在the末端/果胶状肌肉,肺静脉/左心房的交界处,APD出现明显的区域差异。结果,增加了在这些组织连接处所测量的组织对于再次进入的脆弱性。 AF引起的电重塑也稳定并加速了折返激励波,从而导致快速且持续的折返。在房颤重塑的情况下,3D模型中的折返涡旋波退化为持续性和不稳定的小波,从而导致纤颤。总之,现实的3D心房组织模型表明,AF引起的电重构会产生局部异质且缩短的APD。这些分别促进了重入激发波的产生和维持。

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