Sánchez Jorge, Gomez Juan F, Martinez-Mateu Laura, Romero Lucia, Saiz Javier, Trenor Beatriz
Centre for Research and Innovation in Bioengineering, Universitat Politècnica de València, Valencia, Spain.
Front Physiol. 2019 Jul 4;10:847. doi: 10.3389/fphys.2019.00847. eCollection 2019.
Atrial fibrillation (AF), the most common cardiac arrhythmia, is characterized by alteration of the action potential (AP) propagation. Under persistent AF, myocytes undergo electrophysiological and structural remodeling, which involves fibroblast proliferation and differentiation, modifying the substrate for AP propagation. The aim of this study was to analyze the effects on the AP of fibroblast-myocyte coupling during AF and its propagation in different regions of the atria. Isolated myocytes were coupled to different numbers of fibroblasts using the established AP models and tissue simulations were performed by randomly distributing fibroblasts. Fibroblast formulations were updated to match recent experimental data. Major ion current conductances of the myocyte model were modified to simulate AP heterogeneity in four different atrial regions (right atrium posterior wall, crista terminalis, left atrium posterior wall, and pulmonary vein) according to experimental and computational studies. The results of the coupled myocyte-fibroblast simulations suggest that a more depolarized membrane potential and higher fibroblast membrane capacitance have a greater impact on AP duration and myocyte maximum depolarization velocity. The number of coupled fibroblasts and the stimulation frequency are determining factors in altering myocyte AP. Strand simulations show that conduction velocity tends to homogenize in all regions, while the left atrium is more likely to be affected by fibroblast and AP propagation block is more likely to occur. The pulmonary vein is the most affected region, even at low fibroblast densities. In 2D sheets with randomly placed fibroblasts, wavebreaks are observed in the low density (10%) central fibrotic zone and when fibroblast density increases (40%) propagation in the fibrotic region is practically blocked. At densities of 10 and 20% the width of the vulnerable window increases with respect to control but is decreased at 40%. Myocyte-fibroblast coupling characteristics heterogeneously affect AP propagation and features in the different atrial zones, and myocytes from the left atria are more sensitive to fibroblast coupling.
心房颤动(AF)是最常见的心律失常,其特征是动作电位(AP)传播发生改变。在持续性AF状态下,心肌细胞会经历电生理和结构重塑,这涉及成纤维细胞的增殖和分化,从而改变AP传播的基质。本研究的目的是分析AF期间成纤维细胞与心肌细胞耦合对AP的影响及其在心房不同区域的传播情况。使用已建立的AP模型将分离的心肌细胞与不同数量的成纤维细胞耦合,并通过随机分布成纤维细胞进行组织模拟。根据最新实验数据更新了成纤维细胞公式。根据实验和计算研究,修改了心肌细胞模型的主要离子电流电导,以模拟四个不同心房区域(右心房后壁、界嵴、左心房后壁和肺静脉)的AP异质性。成纤维细胞与心肌细胞耦合模拟的结果表明,更去极化的膜电位和更高的成纤维细胞膜电容对AP持续时间和心肌细胞最大去极化速度有更大影响。耦合的成纤维细胞数量和刺激频率是改变心肌细胞AP的决定因素。束状模拟表明,所有区域的传导速度趋于均匀化,而左心房更容易受到成纤维细胞的影响,AP传播阻滞更可能发生。肺静脉是受影响最严重的区域,即使在成纤维细胞密度较低时也是如此。在随机放置成纤维细胞的二维薄片中,在低密度(10%)的中央纤维化区域观察到波裂,当成纤维细胞密度增加(40%)时,纤维化区域的传播实际上被阻断。在10%和20%的密度下,易损窗口的宽度相对于对照组增加,但在40%时减小。成纤维细胞与心肌细胞的耦合特性对不同心房区域的AP传播和特征产生异质性影响,并且左心房的心肌细胞对成纤维细胞耦合更敏感。