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心动过速诱导重塑对兔心房肌细胞钙波传播影响的计算研究

A Computational Study of the Effects of Tachycardia-Induced Remodeling on Calcium Wave Propagation in Rabbit Atrial Myocytes.

作者信息

Vagos Márcia R, Arevalo Hermenegild, Heijman Jordi, Schotten Ulrich, Sundnes Joakim

机构信息

Simula Research Laboratory, Computational Physiology Department, Lysaker, Norway.

Faculty of Health, Medicine and Life Sciences, School for Cardiovascular Diseases, Maastricht, Netherlands.

出版信息

Front Physiol. 2021 Apr 9;12:651428. doi: 10.3389/fphys.2021.651428. eCollection 2021.

Abstract

In atrial cardiomyocytes without a well-developed T-tubule system, calcium diffuses from the periphery toward the center creating a centripetal wave pattern. During atrial fibrillation, rapid activation of atrial myocytes induces complex remodeling in diffusion properties that result in failure of calcium to propagate in a fully regenerative manner toward the center; a phenomenon termed "calcium silencing." This has been observed in rabbit atrial myocytes after exposure to prolonged rapid pacing. Although experimental studies have pointed to possible mechanisms underlying calcium silencing, their individual effects and relative importance remain largely unknown. In this study we used computational modeling of the rabbit atrial cardiomyocyte to query the individual and combined effects of the proposed mechanisms leading to calcium silencing and abnormal calcium wave propagation. We employed a population of models obtained from a newly developed model of the rabbit atrial myocyte with spatial representation of intracellular calcium handling. We selected parameters in the model that represent experimentally observed cellular remodeling which have been implicated in calcium silencing, and scaled their values in the population to match experimental observations. In particular, we changed the maximum conductances of ICaL, INCX, and INaK, RyR open probability, RyR density, Serca2a density, and calcium buffering strength. We incorporated remodeling in a population of 16 models by independently varying parameters that reproduce experimentally observed cellular remodeling, and quantified the resulting alterations in calcium dynamics and wave propagation patterns. The results show a strong effect of ICaL in driving calcium silencing, with INCX, INaK, and RyR density also resulting in calcium silencing in some models. Calcium alternans was observed in some models where INCX and Serca2a density had been changed. Simultaneously incorporating changes in all remodeled parameters resulted in calcium silencing in all models, indicating the predominant role of decreasing ICaL in the population phenotype.

摘要

在没有发育完善的T管系统的心房心肌细胞中,钙从周边向中心扩散,形成向心波模式。在心房颤动期间,心房肌细胞的快速激活会诱导扩散特性的复杂重塑,导致钙无法以完全再生的方式向中心传播;这种现象被称为“钙沉默”。这已在兔心房肌细胞长时间快速起搏后被观察到。尽管实验研究已经指出了钙沉默潜在的可能机制,但其个体效应和相对重要性在很大程度上仍然未知。在本研究中,我们使用兔心房心肌细胞的计算模型来探究导致钙沉默和异常钙波传播的拟议机制的个体效应和联合效应。我们采用了一组从新开发的具有细胞内钙处理空间表示的兔心房肌细胞模型获得的模型。我们在模型中选择了代表实验观察到的与钙沉默有关的细胞重塑的参数,并在群体中缩放其值以匹配实验观察结果。特别是,我们改变了L型钙电流(ICaL)、钠钙交换电流(INCX)和钠钾泵电流(INaK)的最大电导率、兰尼碱受体(RyR)开放概率、RyR密度、肌浆网钙ATP酶2a(Serca2a)密度和钙缓冲强度。我们通过独立改变再现实验观察到的细胞重塑的参数,在16个模型的群体中纳入重塑,并量化钙动力学和波传播模式的由此产生的改变。结果表明,ICaL对驱动钙沉默有很强的作用,在一些模型中,INCX、INaK和RyR密度也导致钙沉默。在一些改变了INCX和Serca2a密度的模型中观察到了钙交替。同时纳入所有重塑参数的变化导致所有模型中出现钙沉默,表明降低ICaL在群体表型中起主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5457/8063103/94fec7ea7013/fphys-12-651428-g0001.jpg

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