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本文引用的文献

1
Increased risk of parkinsonism associated with welding exposure.焊接暴露与帕金森病风险增加相关。
Neurotoxicology. 2012 Oct;33(5):1356-61. doi: 10.1016/j.neuro.2012.08.011. Epub 2012 Sep 3.
2
Basal ganglia intensity indices and diffusion weighted imaging in manganese-exposed welders.基底节区强度指数与锰暴露焊工的弥散加权成像。
Occup Environ Med. 2012 Jun;69(6):437-43. doi: 10.1136/oemed-2011-100119. Epub 2012 Mar 23.
3
Research capacity development in South African manganese mines to bridge exposure and neuropathologic outcomes.南非锰矿的研究能力发展以弥合暴露与神经病理结果之间的差距。
Neurotoxicology. 2012 Aug;33(4):683-6. doi: 10.1016/j.neuro.2012.01.003. Epub 2012 Jan 31.
4
Role of glial cells in manganese neurotoxicity.胶质细胞在锰神经毒性中的作用。
J Appl Toxicol. 2012 May;32(5):310-7. doi: 10.1002/jat.1762. Epub 2011 Nov 26.
5
Role of manganese in neurodegenerative diseases.锰在神经退行性疾病中的作用。
J Trace Elem Med Biol. 2011 Dec;25(4):191-203. doi: 10.1016/j.jtemb.2011.08.144. Epub 2011 Oct 1.
6
Prospective study on neurotoxic effects in manganese-exposed bridge construction welders.前瞻性研究锰暴露于桥梁建筑焊工的神经毒性作用。
Neurotoxicology. 2011 Oct;32(5):596-605. doi: 10.1016/j.neuro.2011.06.004. Epub 2011 Jul 5.
7
Reduced uptake of [¹⁸F]FDOPA PET in asymptomatic welders with occupational manganese exposure.职业性锰暴露无症状焊工[¹⁸F]FDOPA PET 摄取减少。
Neurology. 2011 Apr 12;76(15):1296-301. doi: 10.1212/WNL.0b013e3182152830. Epub 2011 Apr 6.
8
Loss of mitochondrial complex I activity potentiates dopamine neuron death induced by microtubule dysfunction in a Parkinson's disease model.线粒体复合物 I 活性丧失加剧了帕金森病模型中微管功能障碍诱导的多巴胺神经元死亡。
J Cell Biol. 2011 Mar 7;192(5):873-82. doi: 10.1083/jcb.201009132.
9
Statistical modeling to determine sources of variability in exposures to welding fumes.用于确定焊接烟尘暴露变异性来源的统计建模。
Ann Occup Hyg. 2011 Apr;55(3):305-18. doi: 10.1093/annhyg/meq088. Epub 2011 Feb 25.
10
Estimation of particulate mass and manganese exposure levels among welders.焊工中颗粒物质量和锰暴露水平的评估。
Ann Occup Hyg. 2011 Jan;55(1):113-25. doi: 10.1093/annhyg/meq069. Epub 2010 Sep 24.

南非矿工慢性锰暴露相关的定量神经病理学

Quantitative neuropathology associated with chronic manganese exposure in South African mine workers.

作者信息

Gonzalez-Cuyar Luis F, Nelson Gill, Criswell Susan R, Ho Pokuan, Lonzanida Jaymes A, Checkoway Harvey, Seixas Noah, Gelman Benjamin B, Evanoff Bradley A, Murray Jill, Zhang Jing, Racette Brad A

机构信息

Department of Pathology, Division of Neuropathology, University of Washington, School of Medicine, Seattle, WA, USA.

School of Public Health, Faculty of Health Sciences, University of the Witwatersrand, Parktown, South Africa.

出版信息

Neurotoxicology. 2014 Dec;45:260-6. doi: 10.1016/j.neuro.2013.12.008. Epub 2013 Dec 26.

DOI:10.1016/j.neuro.2013.12.008
PMID:24374477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4072755/
Abstract

Manganese (Mn) is a common neurotoxicant associated with a clinical syndrome that includes signs and symptoms referable to the basal ganglia. Despite many advances in understanding the pathophysiology of Mn neurotoxicity in humans, with molecular and structural imaging techniques, only a few case reports describe the associated pathological findings, and all are in symptomatic subjects exposed to relatively high-level Mn. We performed an exploratory, neurohistopathological study to investigate the changes in the corpus striatum (caudate nucleus, putamen, and globus pallidus) associated with chronic low-level Mn exposure in South African Mn mine workers. Immunohistochemical techniques were used to quantify cell density of neuronal and glial components of the corpus striatum in eight South African Mn mine workers without clinical evidence of a movement disorder and eight age-race-gender matched, non-Mn mine workers. There was higher mean microglia density in Mn mine workers than non-Mn mine workers in the globus pallidus external and internal segments [GPe: 1.33 and 0.87 cells per HPF, respectively (p=0.064); GPi: 1.37 and 0.99 cells per HPF, respectively (p=0.250)]. The number of years worked in the Mn mines was significantly correlated with microglial density in the GPi (Spearman's rho 0.886; p=0.019). The ratio of astrocytes to microglia in each brain region was lower in the Mn mine workers than the non-Mn mine workers in the caudate (7.80 and 14.68; p=0.025), putamen (7.35 and 11.11; p=0.117), GPe (10.60 and 16.10; p=0.091) and GPi (9.56 and 12.42; p=0.376). Future studies incorporating more detailed occupational exposures in a larger sample of Mn mine workers will be needed to demonstrate an etiologic relationship between Mn exposure and these pathological findings.

摘要

锰(Mn)是一种常见的神经毒物,与一种临床综合征相关,该综合征包括基底神经节相关的体征和症状。尽管在利用分子和结构成像技术了解人类锰神经毒性的病理生理学方面取得了许多进展,但仅有少数病例报告描述了相关的病理发现,且所有报告均针对接触相对高水平锰的有症状受试者。我们进行了一项探索性神经组织病理学研究,以调查南非锰矿工人慢性低水平锰暴露与纹状体(尾状核、壳核和苍白球)变化之间的关系。采用免疫组织化学技术对8名无运动障碍临床证据的南非锰矿工人以及8名年龄、种族、性别匹配的非锰矿工人纹状体中神经元和胶质细胞成分的细胞密度进行量化。锰矿工人苍白球外部和内部节段的平均小胶质细胞密度高于非锰矿工人[外侧苍白球:分别为每高倍视野1.33个和0.87个细胞(p = 0.064);内侧苍白球:分别为每高倍视野1.37个和0.99个细胞(p = 0.250)]。在锰矿工作的年限与内侧苍白球中的小胶质细胞密度显著相关(斯皮尔曼等级相关系数为0.886;p = 0.019)。在尾状核(分别为7.80和14.68;p = 0.025)、壳核(分别为7.35和11.11;p = 0.117)、外侧苍白球(分别为10.60和16.10;p = 0.091)和内侧苍白球(分别为9.56和12.42;p = 0.376)中,锰矿工人每个脑区的星形胶质细胞与小胶质细胞的比例均低于非锰矿工人。未来需要在更大样本的锰矿工人中开展纳入更详细职业暴露情况的研究,以证明锰暴露与这些病理发现之间的病因学关系。