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Chronotropic Modulation of the Source-Sink Relationship of Sinoatrial-Atrial Impulse Conduction and Its Significance to Initiation of AF: A One-Dimensional Model Study

机译:慢性心房心房冲动传导的源汇关系的调制及其对房颤发作的意义:一维模型研究

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摘要

Initiation and maintenance of atrial fibrillation (AF) is often associated with pharmacologically or pathologically induced bradycardic states. Even drugs specifically developed in order to counteract cardiac arrhythmias often combine their action with bradycardia and, in turn, with development of AF, via still largely unknown mechanisms. This study aims to simulate action potential (AP) conduction between sinoatrial node (SAN) and atrial cells, either arranged in cell pairs or in a one-dimensional strand, where the relative amount of SAN membrane is made varying, in turn, with junctional resistance. The source-sink relationship between the two membrane types is studied in control conditions and under different simulated chronotropic interventions, in order to define a safety factor for pacemaker-to-atrial AP conduction (SASF) for each treatment. Whereas antiarrhythmic-like interventions which involve downregulation of calcium channels or of calcium handling decrease SASF, the simulation of Ivabradine administration does so to a lesser extent. Particularly interesting is the increase of SASF observed when downregulation G Kr, which simulates the administration of class III antiarrhythmic agents and is likely sustained by an increase in I CaL. Also, the increase in SASF is accompanied by a decreased conduction delay and a better entrainment of repolarization, which is significant to anti-AF strategies.
机译:心房颤动(AF)的启动和维持通常与药理或病理学诱发的心动过缓状态有关。即使是专门为抵抗心律不齐而研发的药物,也常常通过很大程度上未知的机制将其作用与心动过缓以及AF的发展结合起来。这项研究的目的是模拟窦房结(SAN)和心房细胞之间的动作电位(AP)传导,该动作电位以细胞对或一维链的形式排列,其中SAN膜的相对量随连接处而变化抵抗性。为了控制起搏器至心房AP传导(SASF)的安全系数,在控制条件下和在不同的模拟变时性干预下研究了两种膜类型之间的源-库关系。涉及钙通道下调或钙处理的抗心律失常样干预措施可降低SASF,而模拟使用伊伐布雷定的效果则较小。特别令人感兴趣的是,当下调G Kr时观察到的SASF升高,这模拟了III类抗心律不齐药物的给药,并可能因I CaL的升高而持续。同样,SASF的增加伴随着传导延迟的减少和复极化的更好夹带,这对于抗AF策略很重要。

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