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脑内注射后甲基汞硫醇复合物的毒性、分布及消除

Toxicity, distribution, and elimination of thiol complexes of methylmercury after intracerebral injection.

作者信息

Fair P H, Balthrop J E, Wade J L, Braddon-Galloway S

出版信息

J Toxicol Environ Health. 1986;19(2):219-33. doi: 10.1080/15287398609530922.

Abstract

Intracerebral injection of CH3Hg and CH3Hg complexed with glutathione (GSH), cysteine (cys), cysteinylglycine (cys-gly), and homocysteine (homocys) resulted in differences in toxicity. Criteria based on neurological indices, mortality, and weight loss indicated that the cys-gly complex of CH3Hg was significantly less toxic than CH3Hg or the other complexes. The other complexes of CH3Hg (GSH, homocys, and cys) were also found to be less toxic than CH3Hg. The selenium status of the animal did not seem to significantly influence the toxicity of CH3Hg and the complexes. While CH3Hg complexed to cys-gly was significantly less toxic than CH3Hg alone, there were no differences observed in the CH3Hg half-life values or in the distribution of these compounds in the kidneys, brain, liver, and blood. It was observed, however, that the CH3Hg--cys-gly complex had higher fecal excretion on d 3 and 4 following intracerebral injection.

摘要

脑内注射甲基汞(CH3Hg)以及与谷胱甘肽(GSH)、半胱氨酸(cys)、半胱氨酰甘氨酸(cys-gly)和同型半胱氨酸(homocys)络合的甲基汞,会导致毒性差异。基于神经学指标、死亡率和体重减轻的标准表明,甲基汞的半胱氨酰甘氨酸络合物的毒性明显低于甲基汞或其他络合物。还发现甲基汞的其他络合物(谷胱甘肽、同型半胱氨酸和半胱氨酸)的毒性也低于甲基汞。动物的硒状态似乎对甲基汞及其络合物的毒性没有显著影响。虽然与半胱氨酰甘氨酸络合的甲基汞的毒性明显低于单独的甲基汞,但在甲基汞的半衰期值或这些化合物在肾脏、大脑、肝脏和血液中的分布方面未观察到差异。然而,观察到在脑内注射后的第3天和第4天,甲基汞-半胱氨酰甘氨酸络合物的粪便排泄量更高。

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