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A NEW STYLE OF DIMETHYLNITROSAMINE INDUCED FULMINANT HEPATITIS IN MICE

机译:二甲基亚硝胺诱导的小鼠恶性肝炎的新样式

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Background: There is still no suitable mice model that can completely mimic the human fulminant hepatitis, which sets a block for drug effect evaluation and mechanism researching of human fulminant hepatitis.Objectives: The aim of this study was to establish an animal model able to mimic the main features of human fulminant hepatitis.Materials and Methods: Dimethylnitrosamine (DMN) was peritoneally injected to mice for liver injury induction. Serum biochemicals, and Prothrombin Time were tested, and Prothrombin activity was calculated, the liver tissue pathological changes were evaluated via macroscopic view observation, HE staining, immunochemical staining, and electron microscopy observation. The mRNA levels of TNF-a, Fas, and IL-1beta were tested with quantitative PCR assay.Results: The serum levels of both ALT and AST were elevated significantly and showed a high plateau. Liver pathological changes were progressed before 48 hours post DMN injection and then started to restore. The mRNA and protein expression levels of TNF-? and IL-1 b were significantly elevated. The PT started to extend from 36 hours and PTA was lower than 40% from then on.Conclusions: This kind of DMN induced mice liver injury is similar to human fulminant hepatitis in main features. This work provided a mice model which could mimic human fulminant hepatitis, and could be valuable for fulminant hepatitis mechanism research and liver protection drug evaluation.
机译:背景:尚无合适的能完全模拟人暴发性肝炎的小鼠模型,为人暴发性肝炎的药效评估和机理研究提供了障碍。目的:本研究的目的是建立一种能够模拟人暴发性肝炎的动物模型。材料与方法:腹腔注射二甲基亚硝胺(DMN)诱导小鼠肝损伤。测试了血清生化试剂和凝血酶原时间,并计算了凝血酶原活性,通过肉眼观察,HE染色,免疫化学染色和电子显微镜观察评价了肝脏组织的病理变化。结果:血清ALT和AST均显着升高,并具有较高的平台性。TNF-α,Fas和IL-1β的mRNA水平通过定量PCR检测。 DMN注射后48小时之前,肝脏病理变化已经进展,然后开始恢复。 TNF-α的mRNA和蛋白质表达水平IL-1b明显升高。 PT从36小时开始延长,PTA从那时开始低于40%。结论:这种DMN诱导的小鼠肝损伤的主要特征与人类暴发性肝炎相似。这项工作提供了一种可以模拟人类暴发性肝炎的小鼠模型,对于暴发性肝炎的机理研究和肝保护药物评估具有重要的价值。

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