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硒化合物可预防甲基汞对幼鼠大脑皮质细胞骨架蛋白体外磷酸化的影响。

Selenium compounds prevent the effects of methylmercury on the in vitro phosphorylation of cytoskeletal proteins in cerebral cortex of young rats.

作者信息

Moretto M B, Funchal C, Zeni G, Pessoa-Pureur R, Rocha J B T

机构信息

Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil.

出版信息

Toxicol Sci. 2005 May;85(1):639-46. doi: 10.1093/toxsci/kfi114. Epub 2005 Feb 16.

Abstract

In this study we investigated the protective ability of the selenium compounds ebselen and diphenyldiselenide against the effect of methylmercury on the in vitro incorporation of 32P into intermediate filament (IF) proteins from the cerebral cortex of 17-day-old rats. We observed that methylmercury in the concentrations of 1 and 5 microM was able to inhibit the phosphorylating system associated with IF proteins without altering the immunocontent of these proteins. Concerning the selenium compounds, diselenide (1, 15, and 50 microM) did not induce alteration of the in vitro phosphorylation of IF proteins. Conversely, 15 microM diselenide was effective in preventing the toxic effects induced by methylmercury. Otherwise, ebselen induced an altered in vitro phosphorylation of the cytoskeletal proteins in a dose-dependent manner. Ebselen at intermediate concentrations (15 and 30 microM) increased the in vitro phosphorylation. However, at low (5 microM) or high (50 and 100 microM) concentrations it was ineffective in altering the cytoskeletal-associated phosphorylating system. Furthermore, 5 microM ebselen presented a protective effect against the action of methylmercury on the phosphorylating system. In conclusion, our results indicate that the selenium compounds ebselen and diselenide present protective actions toward the alterations of the phosphorylating system associated with the IF proteins induced by methylmercury in slices of the cerebral cortex of rats.

摘要

在本研究中,我们探究了硒化合物依布硒啉和二苯基二硒化物对甲基汞作用的保护能力,该作用是针对甲基汞对17日龄大鼠大脑皮质中间丝(IF)蛋白体外掺入32P的影响。我们观察到,浓度为1和5微摩尔的甲基汞能够抑制与IF蛋白相关的磷酸化系统,而不改变这些蛋白的免疫含量。关于硒化合物,二硒化物(1、15和50微摩尔)未引起IF蛋白体外磷酸化的改变。相反,15微摩尔的二硒化物能有效预防甲基汞诱导的毒性作用。此外,依布硒啉以剂量依赖的方式诱导细胞骨架蛋白的体外磷酸化改变。中等浓度(15和30微摩尔)的依布硒啉增加了体外磷酸化。然而,低浓度(5微摩尔)或高浓度(50和100微摩尔)时,它对改变细胞骨架相关的磷酸化系统无效。此外,5微摩尔的依布硒啉对甲基汞对磷酸化系统的作用具有保护作用。总之,我们的结果表明,硒化合物依布硒啉和二硒化物对大鼠大脑皮质切片中甲基汞诱导的与IF蛋白相关的磷酸化系统改变具有保护作用。

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