Department of Pathology, Faculty of Medicine, Institute of Cardiovascular Pathophysiology (INFICA), University of Buenos Aires, 950 J. E. Uriburu, 2nd floor, C1114AAD, Buenos Aires, Argentina.
Institute of Biochemistry and Molecular Medicine (IBIMOL, UBA-CONICET), Buenos Aires, Argentina.
Mol Cell Biochem. 2021 Oct;476(10):3857-3867. doi: 10.1007/s11010-021-04192-4. Epub 2021 Jun 14.
Remote ischemic preconditioning (rIPC) is a cardioprotective phenomenon where brief periods of ischemia followed by reperfusion of one organ/tissue can confer subsequent protection against ischemia/reperfusion injury in other organs, such as the heart. It involves activation of humoral, neural or systemic communication pathways inducing different intracellular signals in the heart. The main purpose of this review is to summarize the possible mechanisms involved in the rIPC cardioprotection, and to describe recent clinical trials to establish the efficacy of these strategies in cardioprotection from lethal ischemia/reperfusion injury. In this sense, certain factors weaken the subcellular mechanisms of rIPC in patients, such as age, comorbidities, medication, and anesthetic protocol, which could explain the heterogeneity of results in some clinical trials. For these reasons, further studies, carefully designed, are necessary to develop a clearer understanding of the pathways and mechanism of early and late rIPC. An understanding of the pathways is important for translation to patients.
远程缺血预处理(rIPC)是一种心肌保护现象,即短暂的器官/组织缺血后再灌注可对其他器官(如心脏)的缺血/再灌注损伤产生后续保护作用。它涉及到体液、神经或全身通讯途径的激活,在心脏中诱导不同的细胞内信号。本综述的主要目的是总结 rIPC 心肌保护中涉及的可能机制,并描述最近的临床试验,以确定这些策略在预防致命性缺血/再灌注损伤中的疗效。在这种情况下,某些因素会削弱患者 rIPC 的亚细胞机制,如年龄、合并症、药物和麻醉方案,这可以解释一些临床试验结果的异质性。出于这些原因,需要进一步精心设计的研究来更清楚地了解早期和晚期 rIPC 的途径和机制。了解途径对于向患者转化很重要。