Yeap Xin-Yi, Dehn Shirley, Adelman Jeremy, Lipsitz Jeremy, Thorp Edward B
Department of Pathology, Feinberg Cardiovascular Research Institute, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Methods Mol Biol. 2013;1004:115-33. doi: 10.1007/978-1-62703-383-1_9.
Myocardial infarction (MI) is death and necrosis of myocardial tissue secondary to ischemia. MI is associated with adverse cardiac remodeling, progressive heart chamber dilation, ventricular wall thinning, and loss of cardiac function. Myocardial necrosis can be experimentally induced in rodents to simulate human MI by surgical occlusion of coronary arteries. When induced in knockout or transgenic mice, this model is useful for the identification of molecular modulators of cell death, cardiac remodeling, and preclinical therapeutic potential. Herein we outline in tandem, methods for microsurgical ligation of the left anterior descending artery followed by quantitation of myocardial necrosis. Necrosis is quantified after staining the heart with triphenyltetrazolium chloride.
心肌梗死(MI)是继发于缺血的心肌组织死亡和坏死。心肌梗死与不良的心脏重塑、进行性心腔扩张、心室壁变薄以及心功能丧失有关。通过手术结扎冠状动脉,可在啮齿动物中实验性诱导心肌坏死以模拟人类心肌梗死。在基因敲除或转基因小鼠中诱导时,该模型可用于识别细胞死亡、心脏重塑的分子调节因子以及临床前治疗潜力。在此,我们依次概述左前降支动脉显微外科结扎方法以及随后心肌坏死定量方法。在用氯化三苯基四氮唑对心脏染色后对坏死进行定量。