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心房内的细胞异质性和复极化:一项计算机模拟研究。

Cellular heterogeneity and repolarisation across the atria: an in silico study.

机构信息

Department of Chemical and Material Engineering, Politecnico Di Milano, 20133, Milan, Italy.

Department of Electronic, Information and Bioengineering, Politecnico Di Milano, 20133, Milan, Italy.

出版信息

Med Biol Eng Comput. 2022 Nov;60(11):3153-3168. doi: 10.1007/s11517-022-02640-x. Epub 2022 Sep 15.

Abstract

Mechanisms of atrial fibrillation and the susceptibility to reentries can be impacted by the repolarization across the atria. Studies into atrial fibrillation ignore cell-to-cell heterogeneity due to electrotonic coupling. Recent studies show that cellular variability may have a larger impact on electrophysiological behaviour than assumed. This paper aims to determine the impact of cellular heterogeneity on the repolarization phase across the AF remodelled atria. Using a population of models approach, 10 anatomically identical atrial models were created to include cellular heterogeneity. Atrial models were compared with an equivalent homogenous model. Activation, APD90, and repolarization maps were used to compare models. The impact of electrotonic coupling in the tissue was determined through a comparison of RMP, APD20, APD50, APD90, and triangulation between regional atrial tissue and the single cell populations. After calibration, cellular heterogeneity does not impact atrial depolarization. Repolarization patterns were significantly impacted by cellular heterogeneity, with the APD90 across the LA increasing due to heterogeneity and the reverse occurring in the RA. Electrotonic coupling caused a reduction in variability across all biomarkers but did not fully remove variability. Electrotonic coupling resulted in an increase in APD20 and APD50, and reduced triangulation compared to isolated cell populations. Heterogeneity also caused a reduction in triangulation compared with regionally homogeneous atria.

摘要

心房颤动的机制和折返易感性可受心房复极的影响。由于电紧张耦合,研究心房颤动时忽略了细胞间的异质性。最近的研究表明,细胞变异性对电生理行为的影响可能比预期的要大。本文旨在确定细胞异质性对房颤重构心房复极相的影响。采用群体模型方法,创建了 10 个解剖学上相同的心房模型来包含细胞异质性。将心房模型与等效的均质模型进行比较。使用激活、APD90 和复极图来比较模型。通过比较组织中的 RMP、APD20、APD50、APD90 和区域心房组织与单细胞群体之间的三角剖分,确定电紧张耦合对组织的影响。在校准后,细胞异质性不会影响心房去极化。复极模式受到细胞异质性的显著影响,LA 中的 APD90 由于异质性而增加,而 RA 中则相反。电紧张耦合降低了所有生物标志物的变异性,但并未完全消除变异性。与孤立的细胞群体相比,电紧张耦合导致 APD20 和 APD50 增加,三角剖分减少。与区域性同质心房相比,异质性也导致三角剖分减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6524/9537222/6cc872a0abb0/11517_2022_2640_Fig1_HTML.jpg

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