Tapin Danielle, Kennedy Greg, Lambert Jean, Zayed Joseph
TOXHUM (Human Toxicology Research Group) and Department of Environmental and Occupational Health, Faculty of Medicine, Université de Montréal, C.P. 6128, Succursale Centre-Ville, Montréal, Québec, Canada, H3C 3J7.
Toxicol Appl Pharmacol. 2006 Mar 1;211(2):166-74. doi: 10.1016/j.taap.2005.07.007. Epub 2005 Aug 19.
Methylcyclopentadienyl manganese tricarbonyl (MMT) is an organic compound that was introduced as an anti-knock additive to replace lead in unleaded fuel. The combustion of MMT results in the emission of fine Mn particulates mainly in the form of manganese sulfate and manganese phosphate. The objective of this study is to determine the effects of subchronic exposure to Mn sulfate in different tissues, on locomotor activity, on neuropathology, and on blood serum biochemical parameters. A control group and three groups of 30 male Sprague-Dawley rats were exposed 6-h/day, 5 days/week for 13 consecutive weeks at 30, 300, or 3,000 microg/m(3) Mn sulfate. Locomotor activity was measured during 36 h using an Auto-Track System. Blood and the following tissues were collected and analyzed for manganese content by neutron activation analysis: olfactory bulb, globus pallidus, caudate/putamen, cerebellum, frontal cortex, liver, lung, testis, and kidney. Neuronal cell counts were obtained for the caudate/putamen and the globus pallidus and clinical biochemistry was assessed. Manganese concentrations were increased in blood, kidney, lung, and testis and in all brain regions in the 3,000 microg/m(3) exposure group. Significant differences were also noted in the 300 microg/m(3) exposure group. Neuronal cell counts for the globus pallidus were significantly different between the two highest exposed groups and the controls. Locomotor activity for all exposure concentrations and resting time for the middle and highest concentrations for the two night resting periods were significantly increased. Total ambulatory count was decreased significantly for all exposure concentrations. Biochemical profiles also presented significant differences. No body weight loss was observed between all groups. These results suggest that neurotoxicity could occur at low exposure levels of Mn sulfate, one of the main combustion products of MMT.
甲基环戊二烯基三羰基锰(MMT)是一种有机化合物,作为抗爆添加剂被引入无铅燃料中以替代铅。MMT燃烧会导致主要以硫酸锰和磷酸锰形式存在的细锰颗粒排放。本研究的目的是确定亚慢性暴露于不同组织中的硫酸锰对运动活性、神经病理学和血清生化参数的影响。将一组对照组和三组每组30只雄性Sprague-Dawley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/立方米的硫酸锰环境中。使用自动跟踪系统在36小时内测量运动活性。采集血液以及以下组织,通过中子活化分析测定锰含量:嗅球、苍白球、尾状核/壳核、小脑、额叶皮质、肝脏、肺、睾丸和肾脏。获得尾状核/壳核和苍白球的神经元细胞计数,并评估临床生化指标。在3000微克/立方米暴露组中,血液、肾脏、肺、睾丸以及所有脑区的锰浓度均升高。在300微克/立方米暴露组中也观察到了显著差异。两个最高暴露组与对照组之间,苍白球的神经元细胞计数存在显著差异。所有暴露浓度下的运动活性以及两个夜间休息期的中高浓度下的休息时间均显著增加。所有暴露浓度下的总行走计数均显著降低。生化指标也呈现出显著差异。所有组之间均未观察到体重减轻。这些结果表明,MMT的主要燃烧产物之一硫酸锰在低暴露水平下可能会产生神经毒性。