Rotors Drift Toward and Stabilize in Low Power Regions in Heterogeneous Models of Atrial Fibrillation.

Laura Martinez-Mateu, Javier Saiz, Omer Berenfeld
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Abstract

Atrial fibrillation (AF) afflicts more than 33 million people worldwide. Success of therapy strategies remains poor and better understanding of the arrhythmia and how to device more effective therapies are needed. The aim of this work is to study the role of electric power distributions in rotors and AF dynamics. For this purpose, single cell and tissue simulations were performed to study the effect of ionic currents gradients and fibrosis in rotor's drifting. The root mean square of the ionic (Pion), capacitance (Pc) and electrotonic (Pele) power was computed over action potentials. Single cell simulations were performed for different values of IK1 and ICaL and number of coupled myofibroblasts. Tissue simulations were performed in presence of IK1 and ICaL gradients and diffused fibrosis. Single cell simulations showed that Pion and Pc increased with IK1, while decreased by increasing ICaL. Increasing the number of coupled myofibroblasts reduced Pion and Pc, whereas Pele increased. Finally, in tissue simulations rotors drifted to regions with low power and anchored in regions with higher density of blunted ionic induced power gradients.

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在非均质房颤模型中,转子向低功率区域漂移并稳定。
全世界有超过3300万人患有心房颤动(AF)。治疗策略的成功率仍然很低,需要更好地了解心律失常以及如何设计更有效的治疗方法。这项工作的目的是研究电力分布在转子和AF动力学中的作用。为此,进行了单细胞和组织模拟,研究了离子电流梯度和纤维化对转子漂移的影响。计算了离子(Pion)、电容(Pc)和电紧张(Pele)功率的均方根除以动作电位。对不同的IK1和ICaL值以及偶联的肌成纤维细胞数量进行单细胞模拟。在IK1和ICaL梯度和弥漫性纤维化存在的情况下进行组织模拟。单细胞模拟结果表明,Pion和Pc随IK1升高而升高,而随ICaL升高而降低。增加偶联肌成纤维细胞的数量,可降低Pion和Pc,而增加Pele。最后,在组织模拟中,转子漂移到低功率区域,锚定在钝化离子诱导功率梯度密度较高的区域。
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