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Effects of Dantrolene on Arrhythmogenicity in Isolated Regional Ischemia-Reperfusion Rabbit Hearts with or without Pacing-Induced Heart Failure

机译:丹特罗对有或无起搏性心力衰竭的局部局部缺血再灌注家兔心律失常的影响

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摘要

Dantrolene was reported to suppress ventricular fibrillation (VF) in failing hearts with acute myocardial infarction, but its antiarrhythmic efficacy in regional ischemia-reperfusion (IR) hearts remains debatable. Heart failure (HF) was induced by right ventricular pacing. The IR rabbit model was created by coronary artery ligation for 30 min, followed by reperfusion for 15 min in vivo in both HF and non-HF groups (n = 9 in each group). Simultaneous voltage and intracellular Ca2+ (Cai) optical mapping was then performed in isolated Langendorff-perfused hearts. Electrophysiological studies were conducted and VF inducibility was evaluated by dynamic pacing. Dantrolene (10 μM) was administered after baseline studies. The HF group had a higher VF inducibility than the control group. Dantrolene had both antiarrhythmic (prolonged action potential duration (APD) and effective refractory period) and proarrhythmic effects (slowed conduction velocity, steepened APD restitution slope, and enhanced arrhythmogenic alternans induction) but had no significant effects on ventricular premature beat (VPB) suppression and VF inducibility in both groups. A higher VF conversion rate in the non-HF group was likely due to greater APD prolonging effects in smaller hearts compared to the HF group. The lack of significant effects on VPB suppression by dantrolene suggests that triggered activity might not be the dominant mechanism responsible for VPB induction in the IR model.
机译:据报道,Dantrolene可以抑制患有急性心肌梗死的心脏衰竭时的心室纤颤(VF),但其在局部缺血再灌注(IR)心脏中的抗心律不齐功效仍然值得商bat。右心室起搏诱发心力衰竭(HF)。 IR兔模型是通过冠状动脉结扎30分钟,然后在HF和非HF组中进行体内再灌注15分钟(每组n = 9)而创建的。然后在孤立的Langendorff灌注心脏中同时进行电压和细胞内Ca 2 + (Cai)光学映射。进行了电生理学研究,并通过动态起搏评估了VF诱导性。基线研究后给予丹特罗(10μm)。 HF组的VF诱导性高于对照组。 Dantrolene具有抗心律不齐(延长动作电位持续时间(APD)和有效不应期)和心律不齐的作用(传导速度减慢,APD复原斜率增加和致心律失常的交替性诱导增强),但对室性早搏(VPB)抑制和两组的VF诱导性。与HF组相比,非HF组中较高的VF转化率可能是由于较小心脏中的APD延长效应更大。 dantrolene对VPB抑制作用缺乏显着影响,提示触发的活性可能不是IR模型中诱导VPB的主要机制。

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