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首页> 外文期刊>Medical electron microscopy >The therapeutic effects of resveratrol on hepatic steatosis in high-fat diet-induced obese mice by improving oxidative stress, inflammation and lipid-related gene transcriptional expression
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The therapeutic effects of resveratrol on hepatic steatosis in high-fat diet-induced obese mice by improving oxidative stress, inflammation and lipid-related gene transcriptional expression

机译:白藜芦醇通过改善氧化应激,炎症和脂质相关基因的转录表达而对高脂饮食诱导的肥胖小鼠肝脂肪变性的治疗作用

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摘要

So far, the majority of the previous animal studies have focused on the preventive effects of resveratrol (RSV) on nonalcoholic fatty liver disease (NAFLD) rather than the therapeutic effects. In this study, the therapeutic effects of RSV on hepatic oxidative stress (OS), inflammation, and lipid metabolism-related gene expression of obese mice induced by a high-fat diet (HFD) were investigated. Male C57BL/6 mice were fed a HFD for 8 weeks to induce obesity-related NAFLD model. And then, NAFLD mice were treated with daily RSV oral gavage at the dose of 100 mg/kg body weight for an additional 4 weeks. HFD-induced the elevation of serum total cholesterol, high-density lipoprotein cholesterol, glucose, insulin, aspar-tate aminotransferase and alanine aminotransferase levels, and homeostasis model assessment of insulin resistance, hepatic histology changes, the increases in hepatic triglyceride, malondialdehyde and tumor necrosis factor alpha concentrations, as well as the higher mRNA expression of hepatic toll-like receptor 4 and cluster of differentiation 36 in mice, were restored by RSV. The therapeutic effects of RSV against hepatic steatosis of HFD obese mice were attributed to the reduction of OS, inflammation and free fatty acid uptake.
机译:迄今为止,大多数先前的动物研究都集中于白藜芦醇(RSV)对非酒精性脂肪肝疾病(NAFLD)的预防作用,而不是治疗作用。在这项研究中,研究了RSV对高脂饮食(HFD)诱导的肥胖小鼠肝氧化应激(OS),炎症和脂质代谢相关基因表达的治疗作用。给雄性C57BL / 6小鼠喂食HFD 8周,以诱导肥胖相关的NAFLD模型。然后,每天以100 mg / kg体重的剂量通过RSV口服管饲NAFLD小鼠,持续4周。 HFD引起血清总胆固醇,高密度脂蛋白胆固醇,葡萄糖,胰岛素,天冬氨酸氨基转移酶和丙氨酸氨基转移酶水平的升高,以及胰岛素抵抗,肝组织学变化,肝甘油三酸酯,丙二醛和肿瘤增加的体内稳态模型评估通过RSV恢复了坏死因子α的浓度,以及小鼠肝脏toll样受体4的较高mRNA表达和分化簇36。 RSV对HFD肥胖小鼠肝脂肪变性的治疗作用归因于OS减少,炎症和游离脂肪酸摄取。

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