Division of Pharmacology & Toxicology, College of Pharmacy, Institute for Cellular & Molecular Biology, and Institute for Neuroscience, The University of Texas at Austin, Austin, TX, USA.
Department of Cell and Developmental Biology, University College London, London, United Kingdom.
J Nutr. 2020 Jun 1;150(6):1360-1369. doi: 10.1093/jn/nxaa066.
Manganese is an essential metal, but elevated brain Mn concentrations produce a parkinsonian-like movement disorder in adults and fine motor, attentional, cognitive, and intellectual deficits in children. Human Mn neurotoxicity occurs owing to elevated exposure from occupational or environmental sources, defective excretion (e.g., due to cirrhosis), or loss-of-function mutations in the Mn transporters solute carrier family 30 member 10 or solute carrier family 39 member 14. Animal models are essential to study Mn neurotoxicity, but in order to be translationally relevant, such models should utilize environmentally relevant Mn exposure regimens that reproduce changes in brain Mn concentrations and neurological function evident in human patients. Here, we provide guidelines for Mn exposure in mice, rats, nematodes, and zebrafish so that brain Mn concentrations and neurobehavioral sequelae remain directly relatable to the human phenotype.
锰是一种必需的金属,但大脑中锰浓度升高会导致成年人出现类似帕金森的运动障碍,儿童则会出现精细运动、注意力、认知和智力缺陷。人类锰神经毒性是由于职业或环境来源暴露增加、排泄缺陷(例如,由于肝硬化)或锰转运蛋白溶质载体家族 30 成员 10 或溶质载体家族 39 成员 14 的功能丧失突变引起的。动物模型对于研究锰神经毒性至关重要,但为了具有转化意义,此类模型应使用环境相关的锰暴露方案,这种方案可重现人类患者大脑中锰浓度和神经功能的变化。在这里,我们提供了在小鼠、大鼠、线虫和斑马鱼中进行锰暴露的指南,以便大脑中锰浓度和神经行为后果与人类表型直接相关。