首页> 外文期刊>Journal of applied toxicology >Role of glutathione conjugation in the hepatotoxicity and immunotoxicity induced by 1-bromopropane in female BALB/c mice.
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Role of glutathione conjugation in the hepatotoxicity and immunotoxicity induced by 1-bromopropane in female BALB/c mice.

机译:谷胱甘肽结合在1-溴丙烷诱导的雌性BALB / c小鼠肝毒性和免疫毒性中的作用。

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摘要

1-Bromopropane (1-BP) is used as a cleaning agent or adhesive solvent in the workplace. In the present study, the hepatotoxic and immunotoxic effects of 1-bromopropane and its conjugation with glutathione (GSH) were investigated in female BALB/c mice. The animals were treated orally with 200, 500 and 1000 mg kg(-1) of 1-BP in corn oil for a dose response study or treated orally with 1000 mg kg(-1) of 1-BP for 6, 12, 24 and 48 h for a time course study. The hepatic and splenic contents of GSH were significantly decreased by 1-BP in a dose-dependent manner. S-propyl GSH was identified in livers following treatment with 1-BP by liquid chromatography-electrospray ionization tandem mass spectrometry. When the production of conjugates from 1-BP was investigated in livers following oral treatment with 1000 mg kg(-1) of 1-BP for 6, 12, 24 and 48 h, the GSH conjugates were detected maximally 6 h after treatment. Treatment of mice with 1-BP increased the serum activity of alanine aminotransferase dose-dependently. The oral 1-BP treatment significantly suppressed the antibody response to a T-dependent antigen and the production of splenic intracellular IL-2 in response to Con A in a dose-dependent manner. The present results suggested that 1-BP could cause hepatotoxicity and immunotoxicity as well as depletion of GSH content due to the formation of GSH conjugates.
机译:1-溴丙烷(1-BP)在工作场所用作清洁剂或粘合剂溶剂。在本研究中,在雌性BALB / c小鼠中研究了1-溴丙烷的肝毒性和免疫毒性及其与谷胱甘肽(GSH)的结合。用剂量分别为200、500和1000 mg kg(-1)的玉米油1-BP口服处理动物以进行剂量反应研究,或采用1000 mg kg(-1)的1-BP口服处理6、12、24。和48小时的时间课程学习。 1-BP以剂量依赖的方式显着降低了GSH的肝和脾含量。通过液相色谱-电喷雾串联质谱法在用1-BP处理后在肝脏中鉴定出S-丙基GSH。当用1000 mg kg(-1)的1-BP口服治疗6、12、24和48小时后,在肝脏中研究了1-BP产生的结合物时,在治疗后最多6小时检测到GSH结合物。用1-BP处理小鼠可剂量依赖性地提高血清丙氨酸转氨酶的活性。口服1-BP治疗以剂量依赖性方式显着抑制抗体对T依赖性抗原的应答和脾细胞内IL-2的应答。目前的结果表明1-BP可能由于GSH缀合物的形成而引起肝毒性和免疫毒性以及GSH含量的减少。

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