Huang Y S
Institute of Burn Research, the First Affiliated Hospital, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical University (the Third Military Medical University), Chongqing 400038, China.
Zhonghua Shao Shang Za Zhi. 2018 Jan 20;34(1):3-7. doi: 10.3760/cma.j.issn.1009-2587.2018.01.002.
It is an important clinical subject to illuminate the mechanisms of myocardial damage in the early stage post severe burn in prevention against and treatment of burn shock, which may offer a targeted " dynamic support" in the treatment of severe burn patients. In recent years, the role of autophagy in hypoxic myocardial injury has attracted much attention. Autophagy is a physiological phenomenon on intracellular digestion process of long-life proteins and the aging and damaged organelles through lysosomal system, and it is essential for maintaining the homeostasis of cells. Severe hypoxia/ischemia causes lysosome dysfunction, insufficient fusion between autophagosome and lysosome, accumulation of autophagosomes, and damaged autophagy flux, thus leading to cell dysfunction and cell death. To study the roles of autophagy and explore the potential signals in autophagy modulation will provide a new therapeutic target for alleviating cardiac dysfunction following severe burn.
阐明严重烧伤后早期心肌损伤的机制对于烧伤休克的防治是一个重要的临床课题,这可能为严重烧伤患者的治疗提供有针对性的“动态支持”。近年来,自噬在缺氧性心肌损伤中的作用备受关注。自噬是通过溶酶体系统对长寿蛋白及衰老和受损细胞器进行细胞内消化的一种生理现象,对维持细胞内稳态至关重要。严重缺氧/缺血会导致溶酶体功能障碍、自噬体与溶酶体融合不足、自噬体积累以及自噬流受损,从而导致细胞功能障碍和细胞死亡。研究自噬的作用并探索自噬调节中的潜在信号,将为减轻严重烧伤后心脏功能障碍提供新的治疗靶点。