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Anti-diabetic effects of emodin involved in the activation of PPAR gamma on high-fat diet-fed and low dose of streptozotocin-induced diabetic mice

机译:大黄素对高脂饮食和低剂量链脲佐菌素诱导的糖尿病小鼠激活PPARγ的抗糖尿病作用

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Rheum palmatum unit has been widely applied in the clinical treatment of diabetes mellitus It has been found that emodin as the major bioactive component of R palmatum L exhibits the competency to activate peroxisomal proliferator-activated receptor-gamma (PPAR gamma) in vitro So the aim of this study was to evaluate the anti-diabetic effects of emodin through the activation of PPAR gamma on high-fat diet-fed and low dose of streptozotocin (STZ)-induced diabetic mice The diabetic mice were intraperitoneally injected with emodin for three weeks No changes of food consumption and the body weight in emodin-treated mice were monitored daily during the entire experiment At the end of experiment. the levels of blood glucose, triglyceride and total cholesterol in serum were significantly decreased after emodin treatment. However, serum high-density lipoprotein cholesterol (HDLc) concentration was significantly elevated The glucose tolerance and insulin sensitivity in emodin-treated group were significantly improved Furthermore, the results of quantitative RT-PCR analysis showed that emodin significantly elevated the mRNA expression level of PPAR gamma and regulated the mRNA expressions of LPL. FAT/CD36, resistin and FABPs (ap2) in liver and adipocyte tissues. No effects on the mRNA expressions of PPAR alpha and PPAR alpha-target genes were observed Taken together, the results suggested that the activation of PPAR gamma and the modulation of metabolism-related genes were likely involved in the anti-diabetic effects of emodin
机译:大黄掌单位已被广泛应用于糖尿病的临床治疗中。已发现大黄素作为大黄掌中主要的生物活性成分,具有在体外激活过氧化物酶体增殖物激活受体-γ(PPARγ)的能力。这项研究的目的是评估大黄素通过激活PPARγ对高脂饮食和低剂量链脲佐菌素(STZ)诱导的糖尿病小鼠的抗糖尿病作用。向糖尿病小鼠腹膜内注射大黄素3周。在整个实验期间,每天监测大黄素处理过的小鼠的食物消耗和体重的变化。在实验结束时。大黄素处理后血清中的血糖,甘油三酸酯和总胆固醇水平明显降低。然而,血清高密度脂蛋白胆固醇(HDLc)浓度显着升高。大黄素治疗组的糖耐量和胰岛素敏感性显着提高。此外,定量RT-PCR分析结果表明,大黄素显着提高了PPAR的mRNA表达水平γ和调节LPL的mRNA表达。肝脏和脂肪细胞组织中的FAT / CD36,抵抗素和FABP(ap2)。综上所述,对PPARα和PPARα靶基因的mRNA表达没有影响,表明PPARγ的激活和代谢相关基因的调节可能与大黄素的抗糖尿病作用有关。

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