Chang Xi-Wen, Zhao An-Peng, Yao Wan-Teng, Li Wen-Bin, Wang Rong
Department of Pharmacy, The 940th Hospital of PLA Joint Logistics Support Force, Lanzhou 730050, China.
School of Pharmacy, Lanzhou University, Lanzhou 730000, China.
Sheng Li Xue Bao. 2023 Apr 25;75(2):255-268.
Cerebral hypoxia often brings irreversible damage to the central nervous system, which seriously endangers human health. It is of great significance to further explore the mechanism of hypoxia-associated brain injury. As a programmed cell death, ferroptosis mainly manifests as cell death caused by excessive accumulation of iron-dependent lipid peroxides. It is associated with abnormal glutathione metabolism, lipid peroxidation and iron metabolism, and is involved in the occurrence and development of various diseases. Studies have found that ferroptosis plays an important role in hypoxia-associated brain injury. This review summarizes the mechanism of ferroptosis, and describes its research progress in cerebral ischemia reperfusion injury, neonatal hypoxic-ischemic brain damage, obstructive sleep apnea-induced brain injury and high-altitude hypoxic brain injury.
脑缺氧常给中枢神经系统带来不可逆损伤,严重危及人类健康。进一步探究缺氧相关脑损伤的机制具有重要意义。铁死亡作为一种程序性细胞死亡,主要表现为铁依赖性脂质过氧化物过度积累导致的细胞死亡。它与谷胱甘肽代谢异常、脂质过氧化及铁代谢相关,参与多种疾病的发生发展。研究发现,铁死亡在缺氧相关脑损伤中起重要作用。本文综述了铁死亡的机制,并阐述了其在脑缺血再灌注损伤、新生儿缺氧缺血性脑损伤、阻塞性睡眠呼吸暂停所致脑损伤及高原缺氧性脑损伤中的研究进展。