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砷诱导的神经毒性:机制评价。

Arsenic-induced neurotoxicity: a mechanistic appraisal.

机构信息

Redox Biology Center, University of Nebraska-Lincoln, Lincoln, NE, 68588, USA.

School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE, 68583, USA.

出版信息

J Biol Inorg Chem. 2019 Dec;24(8):1305-1316. doi: 10.1007/s00775-019-01740-8. Epub 2019 Nov 21.

Abstract

Arsenic is a metalloid found in groundwater as a byproduct of soil/rock erosion and industrial and agricultural processes. This xenobiotic elicits its toxicity through different mechanisms, and it has been identified as a toxicant that affects virtually every organ or tissue in the body. In the central nervous system, exposure to arsenic can induce cognitive dysfunction. Furthermore, iAs has been linked to several neurological disorders, including neurodevelopmental alterations, and is considered a risk factor for neurodegenerative disorders. However, the exact mechanisms involved are still unclear. In this review, we aim to appraise the neurotoxic effects of arsenic and the molecular mechanisms involved. First, we discuss the epidemiological studies reporting on the effects of arsenic in intellectual and cognitive function during development as well as studies showing the correlation between arsenic exposure and altered cognition and mental health in adults. The neurotoxic effects of arsenic and the potential mechanisms associated with neurodegeneration are also reviewed including data from experimental models supporting epidemiological evidence of arsenic as a neurotoxicant. Next, we focused on recent literature regarding arsenic metabolism and the molecular mechanisms that begin to explain how arsenic damages the central nervous system including, oxidative stress, energy failure and mitochondrial dysfunction, epigenetics, alterations in neurotransmitter homeostasis and synaptic transmission, cell death pathways, and inflammation. Outlining the specific mechanisms by which arsenic alters the cell function is key to understand the neurotoxic effects that convey cognitive dysfunction, neurodevelopmental alterations, and neurodegenerative disorders.

摘要

砷是一种类金属,作为土壤/岩石侵蚀以及工业和农业过程的副产品存在于地下水中。这种外源性化学物质通过不同的机制引发其毒性,已被确定为一种影响体内几乎每个器官或组织的有毒物质。在中枢神经系统中,砷暴露可导致认知功能障碍。此外,iAs 已与几种神经紊乱相关联,包括神经发育改变,并且被认为是神经退行性疾病的危险因素。然而,确切的涉及机制仍不清楚。在这篇综述中,我们旨在评估砷的神经毒性作用及其涉及的分子机制。首先,我们讨论了报告砷在发育过程中对智力和认知功能影响的流行病学研究,以及显示砷暴露与认知改变和成年人心理健康之间相关性的研究。还综述了砷的神经毒性作用以及与神经退行性变相关的潜在机制,包括支持流行病学证据表明砷作为神经毒物的实验模型数据。接下来,我们重点关注了最近关于砷代谢和分子机制的文献,这些机制开始解释砷如何损害中枢神经系统,包括氧化应激、能量衰竭和线粒体功能障碍、表观遗传学、神经递质稳态和突触传递的改变、细胞死亡途径和炎症。阐明砷改变细胞功能的具体机制是理解导致认知功能障碍、神经发育改变和神经退行性疾病的神经毒性作用的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f057/6903391/50acc52462a5/nihms-1544170-f0001.jpg

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