Cherry Brandon H, Nguyen Anh Q, Hollrah Roger A, Olivencia-Yurvati Albert H, Mallet Robert T
Brandon H Cherry, Anh Q Nguyen, Roger A Hollrah, Albert H Olivencia-Yurvati, Robert T Mallet, Department of Cardiovascular Research Institute, University of North Texas Health Science Center, Fort Worth, TX 76107, United States.
World J Crit Care Med. 2015 Feb 4;4(1):1-12. doi: 10.5492/wjccm.v4.i1.1.
Cardiac arrest remains a leading cause of death and permanent disability worldwide. Although many victims are initially resuscitated, they often succumb to the extensive ischemia-reperfusion injury inflicted on the internal organs, especially the brain. Cardiac arrest initiates a complex cellular injury cascade encompassing reactive oxygen and nitrogen species, Ca(2+) overload, ATP depletion, pro- and anti-apoptotic proteins, mitochondrial dysfunction, and neuronal glutamate excitotoxity, which injures and kills cells, compromises function of internal organs and ignites a destructive systemic inflammatory response. The sheer complexity and scope of this cascade challenges the development of experimental models of and effective treatments for cardiac arrest. Many experimental animal preparations have been developed to decipher the mechanisms of damage to vital internal organs following cardiac arrest and cardiopulmonary resuscitation (CPR), and to develop treatments to interrupt the lethal injury cascades. Porcine models of cardiac arrest and resuscitation offer several important advantages over other species, and outcomes in this large animal are readily translated to the clinical setting. This review summarizes porcine cardiac arrest-CPR models reported in the literature, describes clinically relevant phenomena observed during cardiac arrest and resuscitation in pigs, and discusses numerous methodological considerations in modeling cardiac arrest/CPR. Collectively, published reports show the domestic pig to be a suitable large animal model of cardiac arrest which is responsive to CPR, defibrillatory countershocks and medications, and yields extensive information to foster advances in clinical treatment of cardiac arrest.
心脏骤停仍然是全球范围内死亡和永久性残疾的主要原因。尽管许多患者最初能够复苏,但他们往往会死于对内脏器官,尤其是大脑造成的广泛缺血再灌注损伤。心脏骤停引发了一系列复杂的细胞损伤级联反应,包括活性氧和氮物种、钙离子超载、三磷酸腺苷(ATP)耗竭、促凋亡和抗凋亡蛋白、线粒体功能障碍以及神经元谷氨酸兴奋性毒性,这些会损伤并杀死细胞,损害内脏器官功能,并引发破坏性的全身炎症反应。这种级联反应的极端复杂性和范围对心脏骤停的实验模型开发和有效治疗构成了挑战。为了解析心脏骤停和心肺复苏(CPR)后重要内脏器官的损伤机制,并开发中断致命损伤级联反应的治疗方法,已经建立了许多实验动物模型。与其他物种相比,猪的心脏骤停和复苏模型具有几个重要优势,并且这种大型动物模型的实验结果很容易转化到临床环境中。本综述总结了文献中报道的猪心脏骤停 - CPR模型,描述了猪心脏骤停和复苏过程中观察到的与临床相关的现象,并讨论了心脏骤停/CPR模型中的众多方法学考虑因素。总体而言,已发表的报告表明家猪是一种合适的心脏骤停大型动物模型,它对CPR、除颤电击和药物有反应,并能提供大量信息以促进心脏骤停临床治疗的进展。