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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Protective Effect of Danhong Injection on Acute Hepatic Failure Induced by Lipopolysaccharide and D-Galactosamine in Mice
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Protective Effect of Danhong Injection on Acute Hepatic Failure Induced by Lipopolysaccharide and D-Galactosamine in Mice

机译:丹洪注射对小鼠脂多糖和D-半乳糖胺诱导的急性肝衰竭的保护作用

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Acute hepatic failure (AHF), which leads to an extremely high mortality rate, has become the focus of attention in clinic. In this study, Danhong injection (DHI) was investigated to evaluate the preventive and protective effect on AHF induced by lipopolysaccharide (LPS) and D-galactosamine (GalN) in mice. For AHF induction, ICR mice were intraperitoneally injected with D-GalN (700 mg/kg) and LPS (20 μg/kg). DHI was administrated twice, at 12 and 1 h, respectively, before D-GalN/LPS injection. After stimulation with D-GalN/LPS for 1 and 6 h, serum and livers were collected for analysis. We found that mice administrated with DHI displayed a higher survival rate, lower serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin (TBil), glutathione S-transferase (GST), and tumor necrosis factor (TNF)-α. DHI inhibited the elevations of hepatic lipid peroxidation (malondialdehyde), caspase-8 activity, and mRNA expression levels of inflammatory cytokines (interleukin-1βand interleukin-6) increased by D-GalN/LPS in the liver. Furthermore, liver histopathological analysis indicated that the DHI group showed markedly fewer apoptotic (TUNEL positive) cells and less pathological changes than those in the AHF model group. These results provide a novel insight into the pharmacological actions of DHI as a potential candidate for treating AHF.
机译:急性肝功能衰竭(AHF)导致极高的死亡率,已成为临床关注的焦点。在这项研究中,研究了丹红注射(DHI),评价对小鼠脂多糖(LPS)和D-半乳糖胺(GALN)诱导的AHF的预防和保护作用。对于AHF诱导,ICR小鼠用D-GALN(700mg / kg)和LPS(20μg/ kg)腹膜内注射。在D-GALN / LPS注射之前,DHI分别在12和1小时,12和1小时施用两次。用D-GALN / LPS刺激1和6小时,收集血清和肝脏进行分析。我们发现用DHI施用的小鼠呈现较高的存活率,降低血清氨基氨基转移酶(ALT),天冬氨酸氨基转移酶(AST),总胆红素(TBIL),谷胱甘肽S转移酶(GST)和肿瘤坏死因子(TNF) -α。 DHI抑制肝脂质过氧化(丙二醛),胱天蛋白酶-8活性的升高和mRNA表达水平(白细胞介素-1β和白细胞介素-6)的D-Galn / LPS在肝脏中增加。此外,肝脏组织病理学分析表明,DHI组显示出凋亡(TUNEL阳性)细胞的显着较少,病理变化比AHF模型组的较少的病理变化。这些结果提供了对DHI的药理作用的新颖洞察力作为治疗AHF的潜在候选者。

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