脂质过氧化
神经毒性
氧化应激
活性氧
谷胱甘肽
抗氧化剂
化学
锰
细胞生物学
GPX4
线粒体
程序性细胞死亡
生物化学
药理学
毒性
生物
细胞凋亡
超氧化物歧化酶
酶
谷胱甘肽过氧化物酶
有机化学
作者
Yaoyang Liu,Shasha Lv,Guo‐Wei He,Changyong Wang,Ou Chen
出处
期刊:Toxicology
[Elsevier BV]
日期:2024-01-01
卷期号:: 153727-153727
标识
DOI:10.1016/j.tox.2024.153727
摘要
Manganese is an essential trace element, but overexposure can cause neurotoxicity and subsequent neurodegenerative diseases. Ferroptosis is a form of cell death characterized by lipid peroxidation and iron overload inside cells, which is closely related to manganese neurotoxicity. Manganese can induce ferroptosis through multiple pathways: causing oxidative stress and increased cellular reactive oxygen species (ROS), resulting in lipid peroxidation; depleting glutathione (GSH) and weakening the antioxidant capacity of cells; disrupting iron metabolism and increasing iron-dependent lipid peroxidation; damaging mitochondrial function and disrupting the electron transport chain, leading to increased ROS production. Oxidative stress, iron metabolism disorders, lipid peroxidation, GSH depletion, and mitochondrial dysfunction, typical features of ferroptosis, have been observed in animal and cell models after manganese exposure. In summary, manganese can participate in the pathogenesis of neurodegenerative diseases by inducing events related to ferroptosis. This provides new insights into studying the mechanism of manganese neurotoxicity and developing therapeutic drugs.
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