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首页> 外文期刊>Nutrition Metabolism >Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats
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Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats

机译:叶酸和褪黑素改善四氯化碳引起的大鼠肝损伤,氧化应激和炎症

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This study investigated the protective effects of melatonin and folic acid against carbon tetrachloride (CCl4)-induced hepatic injury in rats. Oxidative stress, liver function, liver histopathology and serum lipid levels were evaluated. The levels of protein kinase B (Akt1), interferon gamma (IFN-γ), programmed cell death-receptor (Fas) and Tumor necrosis factor-alpha (TNF-α) mRNA expression were analyzed. CCl4 significantly elevated the levels of lipid peroxidation (MDA), cholesterol, LDL, triglycerides, bilirubin and urea. In addition, CCl4 was found to significantly suppress the activity of both catalase and glutathione (GSH) and decrease the levels of serum total protein and HDL-cholesterol. All of these parameters were restored to their normal levels by treatment with melatonin, folic acid or their combination. An improvement of the general hepatic architecture was observed in rats that were treated with the combination of melatonin and folic acid along with CCl4. Furthermore, the CCl4-induced upregulation of TNF-α and Fas mRNA expression was significantly restored by the three treatments. Melatonin, folic acid or their combination also restored the baseline levels of IFN-γ and Akt1 mRNA expression. The combination of melatonin and folic acid exhibited ability to reduce the markers of liver injury induced by CCl4 and restore the oxidative stability, the level of inflammatory cytokines, the lipid profile and the cell survival Akt1 signals.
机译:这项研究调查了褪黑素和叶酸对四氯化碳(CCl4)诱导的大鼠肝损伤的保护作用。评估氧化应激,肝功能,肝组织病理学和血脂水平。分析了蛋白激酶B(Akt1),干扰素γ(IFN-γ),程序性细胞死亡受体(Fas)和肿瘤坏死因子-α(TNF-α)mRNA表达的水平。 CCl4显着提高了脂质过氧化(MDA),胆固醇,LDL,甘油三酸酯,胆红素和尿素的水平。此外,发现CCl4可以显着抑制过氧化氢酶和谷胱甘肽(GSH)的活性,并降低血清总蛋白和HDL-胆固醇的水平。通过褪黑激素,叶酸或其组合治疗,所有这些参数均恢复到正常水平。在褪黑素和叶酸与CCl4联合治疗的大鼠中,观察到总体肝结构的改善。此外,通过三种处理,CCl4诱导的TNF-α和Fas mRNA表达的上调被显着恢复。褪黑素,叶酸或其组合也恢复了IFN-γ和Akt1 mRNA表达的基线水平。褪黑素和叶酸的组合具有减少CCl4诱导的肝损伤标志物,恢复氧化稳定性,炎性细胞因子水平,脂质分布和细胞存活Akt1信号的能力。

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