Salehi Fariba, Normandin Louise, Krewski Daniel, Kennedy Greg, Philippe Suzanne, Zayed Joseph
Department of Environmental and Occupational Health and GRIS (Interdisciplinary Health Research Group), Faculty of Medicine, University of Montreal, Canada.
J Appl Toxicol. 2006 Sep-Oct;26(5):419-26. doi: 10.1002/jat.1156.
In Canada, Methylcyclopentadienyl manganese tricarbonyl (MMT) replaced tetraethyl lead in gasoline as an antiknock agent from 1976 until 2003. The combustion of MMT leads to increased manganese (Mn) concentrations in the atmosphere, and represents one of the main sources of human exposure to Mn. The nervous system is the major target of the toxicity of Mn and Mn compounds. The purpose of this study was to investigate exposure-response relationships for neuropathology and tremor, and the associated electromyogram (EMG), following subchronic inhalation exposure of rats to a mixture of Mn phosphate/sulfate particles. Rats were exposed 6 h per day, 5 days per week for 13 consecutive weeks at 30, 300 or 3000 microg m(-3) Mn phosphate/sulfate mixture and compared with controls. Half of the rats had EMG electrodes implanted in the gastrocnemius muscle of the hind limb to assess tremor at the end of Mn exposure. Two days after the end of Mn exposure, rats were killed by exsanguination and Mn concentrations in the brain (caudate putamen, globus pallidus and frontal cortex) were determined by neutron activation analysis while neuropathology was assessed by counting neuronal cells in 2.5 mm x 2.5 mm grid areas. Increased Mn concentrations were observed in all brain sections at the highest level of exposure. The neuronal cell loss was significantly different in the globus pallidus and the caudate putamen at the highest level of exposure (3000 microg m(-3)). No sign of tremor was observed among the rats. In conclusion, exposure to a high level of Mn phosphate/sulfate mixture brought on neuropathological changes in a specific area of the brain; however, no sign of tremor was observed.
在加拿大,从1976年到2003年,甲基环戊二烯三羰基锰(MMT)取代了汽油中的四乙基铅作为抗爆剂。MMT的燃烧导致大气中锰(Mn)浓度增加,是人类接触Mn的主要来源之一。神经系统是Mn及Mn化合物毒性的主要靶器官。本研究的目的是在大鼠亚慢性吸入暴露于磷酸锰/硫酸锰颗粒混合物后,研究神经病理学和震颤以及相关肌电图(EMG)的暴露-反应关系。大鼠每天暴露6小时,每周5天,连续13周暴露于30、300或3000微克/立方米的磷酸锰/硫酸锰混合物中,并与对照组进行比较。一半的大鼠在Mn暴露结束时在后肢腓肠肌植入EMG电极以评估震颤。Mn暴露结束后两天,通过放血处死大鼠,用中子活化分析法测定大脑(尾状壳核、苍白球和额叶皮质)中的Mn浓度,同时通过在2.5毫米×2.5毫米网格区域内计数神经元细胞来评估神经病理学。在最高暴露水平下,所有脑区的Mn浓度均升高。在最高暴露水平(3000微克/立方米)下,苍白球和尾状壳核中的神经元细胞损失有显著差异。在大鼠中未观察到震颤迹象。总之,暴露于高水平的磷酸锰/硫酸锰混合物会导致大脑特定区域出现神经病理学变化;然而,未观察到震颤迹象。