Lujan Heidi L, DiCarlo Stephen E
Department of Physiology, Wayne State University School of Medicine, Detroit, 48201, Michigan.
Physiol Rep. 2014 Jun 27;2(6). doi: 10.14814/phy2.12057. Print 2014 Jun 1.
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.
在冠状动脉痉挛缓解、不稳定型心绞痛、运动诱发缺血和无症状性缺血期间,可观察到再灌注诱发的致死性室性心律失常。因此,人们正在付出巨大努力来了解导致再灌注诱发致死性心律失常的机制,而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到了再灌注诱发的导致心室颤动(VF)的持续性室性心动过速,但关于小鼠的报道却很少,且成功率有限。重要的是,这些研究均未在完整、清醒的小鼠身上进行。因此,一种用于研究再灌注诱发致死性心律失常的长期植入仪器、完整、清醒的小鼠模型,对于推进驱动心血管治疗的概念和方法可能具有至关重要的意义。因此,我们首次描述了一种用于研究再灌注诱发致死性心律失常的完整、清醒的小鼠模型的应用。对9只雄性小鼠进行仪器植入,以记录心输出量和心电图。此外,在左冠状动脉主干周围放置一个圈套器。恢复后,通过拉动圈套器,在清醒小鼠中确定左冠状动脉主干闭塞3分钟并再灌注所产生的持续性室性心动过速的易感性。在所有9只清醒小鼠中,再灌注均导致了持续性室性心动过速,并最终发展为VF。在转基因研究中常用的C57BL/6J品系的清醒小鼠身上进行的这些操作,可用于基因改造模型,以增强我们对完整、清醒和复杂动物中单个基因缺陷对再灌注诱发致死性室性心律失常影响的理解。