首页> 外文期刊>World Journal of Gastroenterology >Recombinant adenovirus containing hyper-interleukin-6 and hepatocyte growth factor ameliorates acute-on-chronic liver failure in rats
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Recombinant adenovirus containing hyper-interleukin-6 and hepatocyte growth factor ameliorates acute-on-chronic liver failure in rats

机译:含有高白介素6和肝细胞生长因子的重组腺病毒改善大鼠急性肝衰竭

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AIM: To investigate the protective efficacy of recombinant adenovirus containing hyper-interleukin-6 (Hyper-IL-6, HIL-6) and hepatocyte growth factor (HGF) (Ad-HGF-HIL-6) compared to that of recombinant adenovirus containing either HIL-6 or HGF (Ad-HIL-6 or Ad-HGF) in rats with acute-on-chronic liver failure (ACLF). METHODS: The recombinant adenoviruses containing HIL-6 and/or HGF were constructed. We established an ACLF model, and rats were randomly assigned to control, model, Ad-GFP, Ad-HIL-6, Ad-HGF or Ad-HGF-HIL-6 group. We collected serum and liver tissue samples to test pathological changes, biochemical indexes and molecular biological indexes. RESULTS: Attenuated alanine aminotransferase, prothrombin time, high-mobility group box 1 (HMGB1), endotoxin, tumour necrosis factor (TNF)-α and interferon-γ were observed in the Ad-HGF-, Ad-HIL-6- and Ad-HGF-HIL-6-treated rats with ACLF. Likewise, reduced hepatic damage and apoptotic activity, as well as reduced HMGB1 and Bax proteins, but raised expression of Ki67 and Bcl-2 proteins and Bcl-2/Bax ratio were also observed in the Ad-HGF-, Ad-HIL-6- and Ad-HGF-HIL-6-treated rats with ACLF. More significant changes were observed in the Ad-HGF-HIL-6 treatment group without obvious side effects. Furthermore, caspase-3 at the protein level decreased in the Ad-HIL-6 and Ad-HGF-HIL-6 treatment groups, more predominantly in the latter group. CONCLUSION: This study identifies that the protective efficacy of Ad-HGF-HIL-6 is more potent than that of Ad-HGF or Ad-HIL-6 in ACLF rats, with no significant side effects.
机译:目的:研究含有高白介素-6(Hyper-IL-6,HIL-6)和肝细胞生长因子(HGF)(Ad-HGF-HIL-6)的重组腺病毒与含有重组白细胞的腺病毒的保护作用。 HIL-6或HGF(Ad-HIL-6或Ad-HGF)在患有慢性慢性肝衰竭(ACLF)的大鼠中的作用。方法:构建含有HIL-6和/或HGF的重组腺病毒。我们建立了ACLF模型,将大鼠随机分为对照组,模型,Ad-GFP,Ad-HIL-6,Ad-HGF或Ad-HGF-HIL-6组。我们收集了血清和肝组织样本以测试病理变化,生化指标和分子生物学指标。结果:在Ad-HGF-,Ad-HIL-6-和Ad-中观察到了减弱的丙氨酸氨基转移酶,凝血酶原时间,高迁移率第1格盒(HMGB1),内毒素,肿瘤坏死因子(TNF)-α和干扰素-γ。 -HGF-HIL-6治疗的ACLF大鼠。同样,在Ad-HGF-,Ad-HIL-6中也观察到肝损伤和凋亡活性降低,HMGB1和Bax蛋白降低,但Ki67和Bcl-2蛋白表达以及Bcl-2 / Bax比值升高。 -和Ad-HGF-HIL-6治疗的ACLF大鼠。在Ad-HGF-HIL-6治疗组中观察到更明显的变化,而没有明显的副作用。此外,Ad-HIL-6和Ad-HGF-HIL-6治疗组中蛋白质水平的caspase-3降低,在后者组中更为明显。结论:本研究表明,Ad-HGF-HIL-6对ACLF大鼠的保护作用比Ad-HGF或Ad-HIL-6的保护作用更强,且无明显副作用。

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