Quindry John C, Hamilton Karyn L
Cardioprotection Laboratory, Department of Kinesiology, Auburn University, AL 36849, USA.
Curr Cardiol Rev. 2013 Aug;9(3):220-9. doi: 10.2174/1573403x113099990033.
Cardiovascular disease (CVD), including ischemia reperfusion (IR) injury, remains a major cause of morbidity and mortality in industrialized nations. Ongoing research is aimed at uncovering therapeutic interventions against IR injury. Regular exercise participation is recognized as an important lifestyle intervention in the prevention and treatment of CVD and IR injury. More recent understanding reveals that moderate intensity aerobic exercise is also an important experimental model for understanding the cellular mechanisms of cardioprotection against IR injury. An important discovery in this regard was the observation that one-to-several days of exercise will attenuate IR injury. This phenomenon has been observed in young and old hearts of both sexes. Due to the short time course of exercise induced protection, IR injury prevention must be mediated by acute biochemical alterations within the myocardium. Research over the last decade reveals that redundant mechanisms account for exercise induced cardioprotection against IR. While much is now known about exercise preconditioning against IR injury, many questions remain. Perhaps most pressing, is what mechanisms mediate cardioprotection in aged hearts and what sex-dependent differences exist. Given that that exercise preconditioning is a polygenic effect, it is likely that multiple mediators of exercise induced cardioprotection have yet to be uncovered. Also unknown, is whether post translational modifications due to exercise are responsible for IR injury prevention. This review will provide an overview the major mechanisms of IR injury and exercise preconditioning. The discussion highlights many promising avenues for further research and describes how exercise preconditioning may continue to be an important scientific paradigm in the translation of cardioprotection research to the clinic.
心血管疾病(CVD),包括缺血再灌注(IR)损伤,仍然是工业化国家发病和死亡的主要原因。正在进行的研究旨在发现针对IR损伤的治疗干预措施。定期参加体育锻炼被认为是预防和治疗CVD及IR损伤的重要生活方式干预措施。最近的认识表明,中等强度有氧运动也是理解针对IR损伤的心脏保护细胞机制的重要实验模型。在这方面的一个重要发现是观察到一至几天的运动将减轻IR损伤。这种现象在男女老少的心脏中均有观察到。由于运动诱导的保护作用时间较短,IR损伤的预防必须由心肌内的急性生化改变介导。过去十年的研究表明,多种机制共同作用导致运动对IR的心脏保护作用。虽然现在对运动预处理预防IR损伤已经了解很多,但仍有许多问题存在。也许最紧迫的问题是,在老年心脏中介导心脏保护作用的机制是什么,以及存在哪些性别差异。鉴于运动预处理是一种多基因效应,很可能还有多种运动诱导心脏保护作用的介质尚未被发现。同样未知的是,运动引起的翻译后修饰是否负责预防IR损伤。本综述将概述IR损伤和运动预处理的主要机制。讨论突出了许多有前景的进一步研究途径,并描述了运动预处理如何可能继续成为将心脏保护研究转化为临床应用的重要科学范式。