School of Health Sciences, Purdue University, 550 Stadium Mall Drive, Room 1173, West Lafayette, IN, 47907, USA.
Curr Environ Health Rep. 2015 Sep;2(3):315-28. doi: 10.1007/s40572-015-0056-x.
Exposure to manganese (Mn) causes clinical signs and symptoms resembling, but not identical to, Parkinson's disease. Since our last review on this subject in 2004, the past decade has been a thriving period in the history of Mn research. This report provides a comprehensive review on new knowledge gained in the Mn research field. Emerging data suggest that beyond traditionally recognized occupational manganism, Mn exposures and the ensuing toxicities occur in a variety of environmental settings, nutritional sources, contaminated foods, infant formulas, and water, soil, and air with natural or man-made contaminations. Upon fast absorption into the body via oral and inhalation exposures, Mn has a relatively short half-life in blood, yet fairly long half-lives in tissues. Recent data suggest Mn accumulates substantially in bone, with a half-life of about 8-9 years expected in human bones. Mn toxicity has been associated with dopaminergic dysfunction by recent neurochemical analyses and synchrotron X-ray fluorescent imaging studies. Evidence from humans indicates that individual factors such as age, gender, ethnicity, genetics, and pre-existing medical conditions can have profound impacts on Mn toxicities. In addition to body fluid-based biomarkers, new approaches in searching biomarkers of Mn exposure include Mn levels in toenails, non-invasive measurement of Mn in bone, and functional alteration assessments. Comments and recommendations are also provided with regard to the diagnosis of Mn intoxication and clinical intervention. Finally, several hot and promising research areas in the next decade are discussed.
接触锰(Mn)会引起类似于帕金森病的临床症状和体征,但并不完全相同。自 2004 年我们对上一次综述以来,过去十年是 Mn 研究历史上的一个繁荣时期。本报告提供了对 Mn 研究领域新获得的知识的全面综述。新出现的数据表明,除了传统上公认的职业性锰中毒外,Mn 暴露以及由此产生的毒性发生在各种环境背景、营养来源、污染食物、婴儿配方奶粉以及受自然或人为污染的水、土壤和空气中。通过口服和吸入暴露快速吸收到体内后,Mn 在血液中的半衰期相对较短,但在组织中的半衰期相当长。最近的数据表明,Mn 大量积聚在骨骼中,预计人类骨骼中的半衰期约为 8-9 年。最近的神经化学分析和同步加速器 X 射线荧光成像研究表明,Mn 毒性与多巴胺能功能障碍有关。来自人类的证据表明,个体因素,如年龄、性别、种族、遗传和预先存在的医疗条件,可对 Mn 毒性产生深远影响。除了基于体液的生物标志物外,寻找 Mn 暴露生物标志物的新方法包括指甲中的 Mn 水平、骨骼中 Mn 的非侵入性测量以及功能改变评估。还就 Mn 中毒的诊断和临床干预提供了意见和建议。最后,讨论了下一个十年的几个热门和有前途的研究领域。