Icahn School of Medicine at Mount Sinai, New York, USA; University of Brescia, Italy.
Albert Einstein College of Medicine, Bronx, New York, USA.
Neurotoxicology. 2018 Jan;64:1-4. doi: 10.1016/j.neuro.2018.01.002. Epub 2018 Feb 3.
Manganese is an essential trace element, but also at high levels a neurotoxicant. Manganese neurotoxicity has been extensively studied since its discovery in highly exposed workers. The International conference MANGANESE2016 held at the Icahn School of Medicine at Mount Sinai in New York provided relevant updates on manganese research in relation to both occupational and environmental exposures. Epidemiological, toxicological and cellular studies reported at the conference have yielded new insights on mechanisms of manganese toxicity and on opportunities for preventive intervention. Strong evidence now exists for causal associations between manganese and both neurodevelopmental and neurodegenerative disorders. The neurodevelopmental effects of early life exposures are an example of the developmental origin of health and disease (DOHAD) concept. Brain imaging has rapidly become an important tool for examining brain areas impacted by manganese at various life stages. Candidate biomarkers of exposure are being identified in hair, nails, and teeth and reflect different exposure windows and relate to different health outcomes. Sex differences were reported in several studies, suggesting that women are more susceptible. New evidence indicates that the transporter genes SLC30A10 and SLC39A8 influence both manganese homeostasis and toxicity. New potential chelation modalities are being developed.
锰是一种必需的微量元素,但在高浓度下也是一种神经毒素。自从在高度暴露的工人中发现锰的神经毒性以来,人们对其进行了广泛的研究。在纽约西奈山伊坎医学院举行的国际会议“MANGANESE2016”提供了与职业和环境暴露相关的锰研究的最新进展。会议上报告的流行病学、毒理学和细胞研究为锰毒性的机制以及预防干预的机会提供了新的见解。现在有强有力的证据表明,锰与神经发育和神经退行性疾病之间存在因果关系。生命早期暴露的神经发育影响是健康和疾病的发育起源(DOHAD)概念的一个例子。脑成像已迅速成为检查不同生命阶段受锰影响的大脑区域的重要工具。头发、指甲和牙齿中的暴露候选生物标志物正在被识别,它们反映了不同的暴露窗口,并与不同的健康结果相关。几项研究报告了性别差异,表明女性更易受影响。新的证据表明,转运蛋白基因 SLC30A10 和 SLC39A8 影响锰的体内平衡和毒性。新的潜在螯合方式正在开发中。