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首页> 外文期刊>BioMed research international >Simulation of Ectopic Pacemakers in the Heart: Multiple Ectopic Beats Generated by Reentry inside Fibrotic Regions
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Simulation of Ectopic Pacemakers in the Heart: Multiple Ectopic Beats Generated by Reentry inside Fibrotic Regions

机译:心脏异位起搏器的模拟:纤维化区域内折返产生的多个异位搏动

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摘要

The inclusion of nonconducting media, mimicking cardiac fibrosis, in two models of cardiac tissue produces the formation of ectopic beats. The fraction of nonconducting media in comparison with the fraction of healthy myocytes and the topological distribution of cells determines the probability of ectopic beat generation. First, a detailed subcellular microscopic model that accounts for the microstructure of the cardiac tissue is constructed and employed for the numerical simulation of action potential propagation. Next, an equivalent discrete model is implemented, which permits a faster integration of the equations. This discrete model is a simplified version of the microscopic model that maintains the distribution of connections between cells. Both models produce similar results when describing action potential propagation in homogeneous tissue; however, they slightly differ in the generation of ectopic beats in heterogeneous tissue. Nevertheless, both models present the generation of reentry inside fibrotic tissues. This kind of reentry restricted to microfibrosis regions can result in the formation of ectopic pacemakers, that is, regions that will generate a series of ectopic stimulus at a fast pacing rate. In turn, such activity has been related to trigger fibrillation in the atria and in the ventricles in clinical and animal studies.
机译:在两种心脏组织模型中都包含模仿心脏纤维化的非导电性介质,可形成异位搏动。与健康心肌细胞的比例和细胞的拓扑分布相比,非导电介质的比例决定了异位搏动产生的可能性。首先,构建一个详细的亚细胞显微模型,该模型解释了心脏组织的微观结构,并将其用于动作电位传播的数值模拟。接下来,实现等效的离散模型,从而可以更快地积分方程。这种离散模型是微观模型的简化版本,可维持细胞之间连接的分布。当描述动作电位在均质组织中的传播时,两个模型都产生相似的结果。但是,它们在异质组织中异位搏动的产生方面略有不同。尽管如此,这两种模型都显示了纤维化组织内部折返的产生。这种限制进入微纤维化区域的折返会导致异位起搏器的形成,即异位起搏器将以快速的起搏速度产生一系列异位刺激。反过来,在临床和动物研究中,这种活性与在心房和心室中引发纤颤有关。

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