氧化应激
活性氧
一氧化碳中毒
一氧化碳
缺氧(环境)
氧气
化学
氧化磷酸化
线粒体
蛋白质羰基化
氧毒性
程序性细胞死亡
细胞生物学
药理学
医学
生物化学
生物
毒物控制
细胞凋亡
氧化损伤
催化作用
医疗急救
有机化学
作者
Andrey Y. Abramov,Isabella Myers,Plamena R. Angelova
出处
期刊:Antioxidants
[MDPI AG]
日期:2024-09-16
卷期号:13 (9): 1121-1121
标识
DOI:10.3390/antiox13091121
摘要
Despite recent technological progress, carbon monoxide poisoning is still one of the leading causes of domestic and industrial morbidity and mortality. The brain is particularly vulnerable to CO toxicity, and thus the majority of survivors develop delayed movement and cognitive complications. CO binds to haemoglobin in erythrocytes, preventing oxygen delivery to tissues, and additionally inhibits mitochondrial respiration. This renders the effect of CO to be closely related to hypoxia reperfusion injury. Oxygen deprivation, as well as CO poisoning and re-oxygenation, are shown to be able to activate the production of reactive oxygen species and to induce oxidative stress. Here, we review the role of reactive oxygen species production and oxidative stress in the mechanism of neuronal cell death induced by carbon monoxide and re-oxygenation. We discuss possible protective mechanisms used by brain cells with a specific focus on the inhibition of CO-induced ROS production and oxidative stress.
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