Naito Hiromichi, Nojima Tsuyoshi, Fujisaki Noritomo, Tsukahara Kohei, Yamamoto Hirotsugu, Yamada Taihei, Aokage Toshiyuki, Yumoto Tetsuya, Osako Takaaki, Nakao Atsunori
Department of Emergency, Critical Care and Disaster Medicine Okayama University Graduate School of Medicine Dentistry and Pharmaceutical Sciences Okayama Japan.
Acute Med Surg. 2020 Apr 13;7(1):e501. doi: 10.1002/ams2.501. eCollection 2020 Jan-Dec.
Ischemia reperfusion (IR) injury occurs when blood supply, perfusion, and concomitant reoxygenation is restored to an organ or area following an initial poor blood supply after a critical time period. Ischemia reperfusion injury contributes to mortality and morbidity in many pathological conditions in emergency medicine clinical practice, including trauma, ischemic stroke, myocardial infarction, and post-cardiac arrest syndrome. The process of IR is multifactorial, and its pathogenesis involves several mechanisms. Reactive oxygen species are considered key molecules in reperfusion injury due to their potent oxidizing and reducing effects that directly damage cellular membranes by lipid peroxidation. In general, IR injury to an individual organ causes various pro-inflammatory mediators to be released, which could then induce inflammation in remote organs, thereby possibly advancing the dysfunction of multiple organs. In this review, we summarize IR injury in emergency medicine. Potential therapies include pharmacological treatment, ischemic preconditioning, and the use of medical gases or vitamin therapy, which could significantly help experts develop strategies to inhibit IR injury.
缺血再灌注(IR)损伤是指在一段关键时间后,当血液供应、灌注以及随之而来的再氧合作用恢复到最初血液供应不足的器官或区域时所发生的损伤。缺血再灌注损伤在急诊医学临床实践中的许多病理状况下,包括创伤、缺血性中风、心肌梗死和心脏骤停后综合征,都会导致死亡率和发病率上升。IR过程是多因素的,其发病机制涉及多种机制。由于活性氧具有强大的氧化和还原作用,可通过脂质过氧化直接损伤细胞膜,因此被认为是再灌注损伤中的关键分子。一般来说,单个器官的IR损伤会导致多种促炎介质释放,进而可能诱发远处器官的炎症,从而可能导致多器官功能障碍。在本综述中,我们总结了急诊医学中的IR损伤。潜在的治疗方法包括药物治疗、缺血预处理以及使用医用气体或维生素疗法,这可能会显著帮助专家们制定抑制IR损伤的策略。