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三羰基甲基环戊二烯基锰(MMT)对小鼠的神经毒性作用:MMT诱导癫痫发作活动的基础。

Neurotoxic effects of methylcyclopentadienyl manganese tricarbonyl (MMT) in the mouse: basis of MMT-induced seizure activity.

作者信息

Fishman B E, McGinley P A, Gianutsos G

出版信息

Toxicology. 1987 Aug;45(2):193-201. doi: 10.1016/0300-483x(87)90105-3.

DOI:10.1016/0300-483x(87)90105-3
PMID:3603584
Abstract

Methylcyclopentadienyl manganese tricarbonyl (MMT) is an organic manganese-containing compound which is used as an additive in unleaded gasoline. One neurotoxic effect of MMT in mice is seizure activity. In this study, seizures were observed in mice treated with MMT in propylene glycol or corn oil. The LD50 associated with seizure activity was lower in mice receiving MMT in propylene glycol (152 mg/kg) than in those receiving MMT in corn oil (999 mg/kg). Manganese concentrations in the brains of mice which showed seizure activity due to MMT were higher than in those that did not (2.45 micrograms/g vs. 1.14 micrograms/g for MMT treated in propylene glycol and 3.25 micrograms/g vs. 1.63 micrograms/g for MMT in corn oil). Mice treated with manganese chloride (MnCl2) showed increases in brain manganese comparable to those of the mice showing seizure activity due to MMT, but exhibited no sign of seizure activity. MMT in non-lethal seizure-inducing doses had no effect on the accumulation of 4-aminobutyric acid (GABA) in mouse brain. However, MMT inhibited the binding of t-[3H]t-butylbicycloorthobenzoate [3H]-TBOB (a ligand for the GABA-A-receptor linked chloride channel) in mouse brain membranes with an IC50 value of 22.8 microM. The data suggest that MMT (organic manganese) or a closely related metabolite and not elemental manganese itself is responsible for the seizure activity observed. The seizure activity may be the result of an inhibitory effect of MMT at the GABA-A receptor linked chloride channel.

摘要

甲基环戊二烯三羰基锰(MMT)是一种含锰有机化合物,用作无铅汽油的添加剂。MMT对小鼠的一种神经毒性作用是引发癫痫活动。在本研究中,观察到用丙二醇或玉米油中的MMT处理的小鼠出现癫痫发作。与癫痫活动相关的半数致死剂量(LD50)在接受丙二醇中MMT的小鼠中(152毫克/千克)低于接受玉米油中MMT的小鼠(999毫克/千克)。因MMT而出现癫痫活动的小鼠大脑中的锰浓度高于未出现癫痫活动的小鼠(丙二醇中MMT处理的小鼠为2.45微克/克对1.14微克/克,玉米油中MMT处理的小鼠为3.25微克/克对1.63微克/克)。用氯化锰(MnCl2)处理的小鼠大脑中的锰含量增加,与因MMT而出现癫痫活动的小鼠相当,但未表现出癫痫活动迹象。非致死性诱发癫痫剂量的MMT对小鼠大脑中4-氨基丁酸(GABA)的积累没有影响。然而,MMT抑制小鼠脑膜中t-[3H]叔丁基双环邻苯二甲酸酯[3H]-TBOB(GABA-A受体连接氯离子通道的配体)的结合,IC50值为22.8微摩尔。数据表明,MMT(有机锰)或与其密切相关的代谢物而非元素锰本身是观察到的癫痫活动的原因。癫痫活动可能是MMT对GABA-A受体连接氯离子通道产生抑制作用的结果。

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