Suppr超能文献

有机汞化合物的神经毒性。

Neurotoxicity of organomercurial compounds.

作者信息

Sanfeliu Coral, Sebastià Jordi, Cristòfol Rosa, Rodríguez-Farré Eduard

机构信息

Department of Pharmacology and Toxicology, Institut d'Investigacions Biomèdiques de Barcelona, CSIC, IDIBAPS, Rossellò 161, 08036 Barcelona, Spain.

出版信息

Neurotox Res. 2003;5(4):283-305. doi: 10.1007/BF03033386.

Abstract

Mercury is a ubiquitous contaminant, and a range of chemical species is generated by human activity and natural environmental change. Elemental mercury and its inorganic and organic compounds have different toxic properties, but all them are considered hazardous in human exposure. In an equimolecular exposure basis, organomercurials with a short aliphatic chain are the most harmful compounds and they may cause irreversible damage to the nervous system. Methylmercury (CH(3)Hg(+)) is the most studied following the neurotoxic outbreaks identified as Minamata disease and the Iraq poisoning. The first description of the CNS pathology dates from 1954. Since then, the clinical neurology, the neuropathology and the mechanisms of neurotoxicity of organomercurials have been widely studied. The high thiol reactivity of CH(3)Hg(+), as well as all mercury compounds, has been suggested to be the basis of their harmful biological effects. However, there is clear selectivity of CH(3)Hg(+) for specific cell types and brain structures, which is not yet fully understood. The main mechanisms involved are inhibition of protein synthesis, microtubule disruption, increase of intracellular Ca(2+) with disturbance of neurotransmitter function, oxidative stress and triggering of excitotoxicity mechanisms. The effects are more damaging during CNS development, leading to alterations of the structure and functionality of the nervous system. The major source of CH(3)Hg(+) exposure is the consumption of fish and, therefore, its intake is practically unavoidable. The present concern is on the study of the effects of low level exposure to CH(3)Hg(+) on human neurodevelopment, with a view to establishing a safe daily intake. Recommendations are 0.4 micro g/kg body weight/day by the WHO and US FDA and, recently, 0.1 micro g/kg body weight/day by the US EPA. Unfortunately, these levels are easily attained with few meals of fish per week, depending on the source of the fish and its position in the food chain.

摘要

汞是一种普遍存在的污染物,人类活动和自然环境变化会产生一系列汞的化学物种。元素汞及其无机和有机化合物具有不同的毒性特性,但所有这些在人体接触时都被视为有害物质。在等分子接触的基础上,具有短脂肪链的有机汞化合物是最有害的化合物,它们可能会对神经系统造成不可逆转的损害。甲基汞(CH(3)Hg(+))是在被认定为水俣病和伊拉克中毒事件的神经毒性爆发后研究最多的。中枢神经系统病理学的首次描述可追溯到1954年。从那时起,有机汞化合物的临床神经学、神经病理学和神经毒性机制就得到了广泛研究。CH(3)Hg(+)以及所有汞化合物的高硫醇反应性被认为是其有害生物学效应的基础。然而,CH(3)Hg(+)对特定细胞类型和脑结构具有明显的选择性,这一点尚未完全理解。主要涉及的机制包括抑制蛋白质合成、微管破坏、细胞内Ca(2+)增加并伴有神经递质功能紊乱、氧化应激以及引发兴奋性毒性机制。这些影响在中枢神经系统发育期间更具破坏性,会导致神经系统结构和功能的改变。CH(3)Hg(+)暴露的主要来源是食用鱼类,因此实际上难以避免摄入。目前关注的是低水平接触CH(3)Hg(+)对人类神经发育的影响研究,以期确定安全的每日摄入量。世界卫生组织和美国食品药品监督管理局建议的摄入量为0.4微克/千克体重/天,最近美国环境保护局建议的摄入量为0.1微克/千克体重/天。不幸的是,根据鱼类的来源及其在食物链中的位置,每周只需吃几餐鱼就很容易达到这些水平。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验