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Establishment of a new animal model of azithromycin-induced liver injury and study the molecular pathological change during the process

机译:建立阿奇霉素引起的肝损伤新动物模型并研究其过程中的分子病理变化

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The purpose of the present study is to establish a new animal model of azithromycin (AZ)-induced liver injury and study the molecular pathological change during the process. First, mice were respectively injected intraperitoneally with AZ of different high doses. Our results showed that 800 mg/kg AZ injection significantly induced liver injury in the mice, which reflected an ideal process of liver injury and repair. In this study, we analyzed the molecular pathological changes during the process by hematoxylin and eosin staining, immunohistochemistry, Western blot, and quantitative real-time reverse transcription polymerase chain reaction in the liver of mice at 0, 12, 24, 48, and 72 h after 800 mg/kg injection. Our results showed that the expression of heat shock protein 70, proliferating cell nuclear antigen, vascular endothelial growth factor, caspase 3, and cytochrome P450 2E1 were significantly differently expressed during liver injury induced by 800 mg/kg AZ in mice. Our results will be conducive for further study of the pathogenesis and prevention of drug-induced liver injury.
机译:本研究的目的是建立阿奇霉素(AZ)引起的肝损伤的新动物模型,并研究该过程中的分子病理学变化。首先,分别给小鼠腹膜内注射不同高剂量的AZ。我们的结果表明,800 mg / kg AZ注射显着诱导小鼠肝损伤,这反映了理想的肝损伤和修复过程。在这项研究中,我们通过苏木精和曙红染色,免疫组化,Western印迹和定量实时逆转录聚合酶链反应在小鼠肝脏中0、12、24、48和72的变化过程中的分子病理学变化进行了分析。注射800 mg / kg后h。我们的结果表明,在800 mg / kg AZ诱发的小鼠肝损伤中,热休克蛋白70,增殖细胞核抗原,血管内皮生长因子,caspase 3和细胞色素P450 2E1的表达明显不同。我们的结果将有助于进一步研究药物性肝损伤的发病机理和预防。

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