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金属神经毒性中的小胶质细胞激活:对神经退行性疾病的影响。

Microglial Activation in Metal Neurotoxicity: Impact in Neurodegenerative Diseases.

机构信息

Departamento de Toxicología, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Mexico City 07360, Mexico.

出版信息

Biomed Res Int. 2023 Jan 31;2023:7389508. doi: 10.1155/2023/7389508. eCollection 2023.

Abstract

Neurodegenerative processes encompass a large variety of diseases with different pathological patterns and clinical features, such as Alzheimer's and Parkinson's diseases. Exposure to metals has been hypothesized to increase oxidative stress in brain cells leading to cell death and neurodegeneration. Neurotoxicity of metals has been demonstrated by several and experimental studies, and most probably, each metal has its specific pathway to trigger cell death. As a result, exposure to essential metals, such as manganese, iron, copper, zinc, and cobalt, and nonessential metals, including lead, aluminum, and cadmium, perturbs metal homeostasis at the cellular and organism levels leading to neurodegeneration. In this contribution, a comprehensive review of the molecular mechanisms by which metals affect microglia physiology and signaling properties is presented. Furthermore, studies that validate the disruption of microglia activation pathways as an essential mechanism of metal toxicity that can contribute to neurodegenerative disease are also presented and discussed.

摘要

神经退行性过程包含多种具有不同病理模式和临床特征的疾病,如阿尔茨海默病和帕金森病。有假说认为,金属暴露会增加脑细胞中的氧化应激,导致细胞死亡和神经退行性变。多项 和 实验研究证明了金属的神经毒性,而且很可能每种金属都有其触发细胞死亡的特定途径。因此,暴露于必需金属(如锰、铁、铜、锌和钴)和非必需金属(包括铅、铝和镉)会扰乱细胞和机体水平的金属内稳态,导致神经退行性变。在本综述中,全面回顾了金属影响小胶质细胞生理和信号特性的分子机制。此外,还提出并讨论了一些研究,这些研究验证了小胶质细胞激活途径的破坏是金属毒性的一个重要机制,可能导致神经退行性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd7/9904912/88f6ab2e072a/BMRI2023-7389508.001.jpg

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