金属污染物通过铁下垂诱导神经毒性的研究进展。

Q2 Medicine
Ziyu Qin, Yuqing Chen, Xinyuan Zhao, Shali Yu
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引用次数: 0

摘要

已经证实,接触各种金属污染物会诱发神经中毒,这与神经系统疾病的发生和发展密切相关。铁变态反应是细胞因接触金属污染物而死亡的一种形式,它与氧化应激、铁代谢和脂质过氧化密切相关。最近的研究发现,铁突变在铅、镉、锰、镍和锑等金属诱发的神经毒性中起着重要作用。铅暴露会通过氧化应激、铁代谢紊乱和炎症引发铁变态反应。镉可通过铁离子代谢、氧化应激和与铁变态反应相关的信号通路(如 IRE1/JNK/FTH1)诱导铁变态反应。锰可通过线粒体功能障碍、铁代谢紊乱和氧化应激促进铁氧化。镍可通过影响线粒体功能、破坏铁平衡和促进中枢神经系统的脂质过氧化来促进铁中毒。锑暴露可通过激活铁的自噬作用诱发谷胱甘肽耗竭,导致细胞内铁过度沉积,最终引起铁变态反应。本文回顾了金属污染物对铁变态反应相关指标的影响,并讨论了每种金属引发铁变态反应的具体机制。它可为确定预防神经毒性的靶点和制定神经系统疾病的治疗策略提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Research progress on metal pollutants inducing neurotoxicity through ferroptosis].

It has been confirmed that exposure to various metal pollutants can induce neurotoxicity, which is closely associated with the occurrence and development of neurological disorders. Ferroptosis is a form of cell death in response to metal pollutant exposure and it is closely related to oxidative stress, iron metabolism and lipid peroxidation. Recent studies have revealed that ferroptosis plays a significant role in the neurotoxicity induced by metals such as lead, cadmium, manganese, nickel, and antimony. Lead exposure triggers ferroptosis through oxidative stress, iron metabolism disorder and inflammation. Cadmium can induce ferroptosis through iron metabolism, oxidative stress and ferroptosis related signaling pathways. Manganese can promote ferroptosis through mitochondrial dysfunction, iron metabolism disorder and oxidative stress. Nickel can promote ferroptosis by influencing mitochondrial function, disrupting iron homeostasis and facilitating lipid peroxidation in the central nervous system. Antimony exposure can induce glutathione depletion by activating iron autophagy, resulting in excessive intracellular iron deposition and ultimately causing ferroptosis. This article reviews the effects of metal pollutants on ferroptosis-related indicators and discusses the specific mechanisms by which each metal triggers ferroptosis. It provides a reference for identifying targets for preventing neurotoxicity and for developing treatment strategies for neurological disorders.

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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
67
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