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Reperfusion‐induced sustained ventricular tachycardia leading to ventricular fibrillation in chronically instrumented intact conscious mice

机译:再灌注引起的持续性室性心动过速导致慢性仪器化的完整的意识清醒的小鼠

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摘要

Reperfusion‐induced lethal ventricular arrhythmias are observed during relief of coronary artery spasm, with unstable angina, exercise‐induced ischemia, and silent ischemia. Accordingly, significant efforts are underway to understand the mechanisms responsible for reperfusion‐induced lethal arrhythmias and mice have become increasingly important in these efforts. However, although reperfusion‐induced sustained ventricular tachycardia leading to ventricular fibrillation (VF) has been recorded in many models, reports in mice are sparse and of limited success. Importantly, none of these studies were conducted in intact, conscious mice. Accordingly, a chronically instrumented, intact, conscious murine model of reperfusion‐induced lethal arrhythmias has the potential to be of major importance for advancing the concepts and methods that drive cardiovascular therapies. Therefore, we describe, for the first time, the use of an intact, conscious, murine model of reperfusion‐induced lethal arrhythmias. Male mice (n = 9) were instrumented to record cardiac output and the electrocardiogram. In addition, a snare was placed around the left main coronary artery. Following recovery, the susceptibility to sustained ventricular tachycardia produced by 3 min of occlusion and reperfusion of the left main coronary artery was determined in conscious mice by pulling on the snare. Reperfusion culminated in sustained ventricular tachycardia, leading to VF, in all nine conscious mice. The procedures conducted in conscious C57BL/6J mice, a strain commonly used in transgenic studies, can be utilized in genetically modified models to enhance our understanding of single gene defects on reperfusion‐induced lethal ventricular arrhythmias in intact, conscious, and complex animals.
机译:在冠状动脉痉挛缓解期间观察到由再灌注引起的致死性室性心律失常,伴不稳定的心绞痛,运动诱发的缺血和无症状的缺血。因此,正在进行大量努力来了解引起再灌注致死性心律失常的机制,并且小鼠在这些努力中变得越来越重要。然而,尽管在许多模型中都记录了由再灌注引起的持续性室性心动过速导致室颤(VF),但有关小鼠的报道稀少且成功率有限。重要的是,这些研究均未在完整的清醒小鼠中进行。因此,一种长期使用的,完整的,有意识的鼠类模型,具有再灌注诱导的致死性心律失常的潜力,对推进驱动心血管疗法的概念和方法具有重要意义。因此,我们首次描述了使用完整,自觉的鼠模型,用于再灌注诱导的致死性心律失常。雄性小鼠(n = 9)被仪器记录心输出量和心电图。另外,在左主冠状动脉周围放置圈套器。恢复后,通过拉除圈套器,在有意识的小鼠中确定左主冠状动脉闭塞和再灌注3分钟对持续性室性心动过速的敏感性。在所有九只意识清醒的小鼠中,再灌注最终导致持续的室性心动过速,从而导致VF。在有意识的C57BL / 6J小鼠(转基因研究中常用的一种菌株)中进行的程序可用于转基因模型中,以增进我们对完整,有意识和复杂动物中再灌注引起的致死性室性心律失常的单基因缺陷的了解。

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