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首页> 外文期刊>The Journal of toxicological sciences >Carbon tetrachloride-induced lethality in mouse is prevented by multiple pretreatment with zinc sulfate
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Carbon tetrachloride-induced lethality in mouse is prevented by multiple pretreatment with zinc sulfate

机译:硫酸锌多次预处理可防止四氯化碳诱导的小鼠致死性

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摘要

Carbon tetrachloride (CCl4) is commonly used as a chemical inducer of experimental liver injury. Several compounds have been demonstrated to attenuate the hepatic damage caused by sublethal doses of CCl4. However, rescue from lethal toxicity of CCl4 has not been reported. In the present study, we evaluated the protective effect of metallothionein (MT), an endogenous scavenger of free radicals, on CCl4-induced lethal toxicity of mice. To induce MT production in male ddY mice, we administered Zn (as ZnSO4) at 50 mg/kg as a once-daily subcutaneous injection for 3 days prior to a single intraperitoneal administration of 4 g/kg CCl4. Animals were observed for mortality every 3 hr for 24 hr after CCl4 injection. Liver damage was assessed by determining (in a subset of these mice) blood levels of alanine aminotransferase (ALT; a marker of liver injury) and liver histopathology at 6 hr after CCl4 injection. Our results showed that three times pretreatment with Zn yielded > 40-fold induction of hepatic MT protein levels compared to control group. Zn pretreatment completely abolished the CCl4-induced mortality of mice. We also found that pretreatment of mice with Zn significantly decreased the ALT levels and reduced the histological liver damage as assessed at 6 hr post-CCl4. These findings suggest that prophylaxis with Zn protects mice from CCl4-induced acute hepatic toxicity and mortality, presumably by induction of radical-scavenging MT.
机译:四氯化碳(CCl 4 )通常用作实验性肝损伤的化学诱导剂。已证明几种化合物可减轻亚致死剂量的CCl 4 对肝脏的损害。然而,尚无从CCl 4 致死毒性中解救的报道。在本研究中,我们评估了内源性自由基清除剂金属硫蛋白(MT)对CCl 4 诱导的小鼠致死毒性的保护作用。为了诱导雄性ddY小鼠的MT产生,我们以每天一次皮下注射的方式每天一次皮下注射50 mg / kg的Zn(以ZnSO 4 )3天,然后一次腹膜内给药4 g / kg CCl 4 。注射CCl 4 后每24小时每3小时观察一次动物死亡率。在注射CCl 4 后6小时,通过测定(在这些小鼠的一部分中)丙氨酸氨基转移酶(ALT;肝损伤的标志物)的血液水平和肝组织病理学来评估肝损伤。我们的结果表明,与对照组相比,锌的三倍预处理可诱导> 40倍的肝MT蛋白水平诱导。锌预处理完全消除了CCl 4 诱导的小鼠死亡率。我们还发现,在CCl 4 后6小时评估,用Zn预处理的小鼠可显着降低ALT水平并减少组织学肝损伤。这些发现表明,锌的预防可能通过诱导自由基清除MT来保护小鼠免受CCl 4 诱导的急性肝毒性和死亡。

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