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首页> 外文期刊>Journal of Translational Medicine >The Chinese herbal medicine FTZ attenuates insulin resistance via IRS1 and PI3K in vitro and in rats with metabolic syndrome
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The Chinese herbal medicine FTZ attenuates insulin resistance via IRS1 and PI3K in vitro and in rats with metabolic syndrome

机译:中药FTZ通过IRS1和PI3K在体外和代谢综合征大鼠中减弱胰岛素抵抗

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Background Insulin resistance plays an important role in the development of metabolic syndrome (MS). Fu Fang Zhen Zhu Tiao Zhi formula (FTZ), a Chinese medicinal decoction, has been used to relieve hyperlipidemia, atherosclerosis and other symptoms associated with metabolic disorders in the clinic. Methods To evaluate the effect of FTZ on insulin resistance, HepG2 cells were induced with high insulin as a model of insulin resistance and treated with FTZ at one of three dosages. Next, the levels of glucose content, insulin receptor substrate1 (IRS1) protein expression and phosphatidylinositol 3-kinase (PI3K) subunit p85 mRNA expression were measured. Alternatively, MS was induced in rats via gavage feeding of a high-fat diet for four consecutive weeks followed by administration of FTZ for eight consecutive weeks. Body weight and the plasma levels of lipids, insulin and glucose were evaluated. Finally, the expression of PI3K p85 mRNA in adipose tissue of rats was measured. Results Our results revealed that FTZ attenuated glucose content and up-regulated the expression of PI3K p85 mRNA and IRS1 protein in insulin-resistant HepG2 cells in vitro. Moreover, FTZ reduced body weight and the plasma concentrations of triacylglycerol, cholesterol, fasting glucose and insulin in insulin resistant MS rats. FTZ also elevated the expression of PI3K p85 mRNA in the adipose tissues of MS rats. Conclusion FTZ attenuated MS symptoms by decreasing the plasma levels of glucose and lipids. The underlying mechanism was attenuation of the reduced expression of PI3K p85 mRNA and IRS1 protein in both insulin-resistant HepG2 cells and MS rats.
机译:背景技术胰岛素抵抗在代谢综合征(MS)的发展中起着重要作用。复方珍竹调脂配方(FTZ)是一种中药汤剂,已被用于缓解高脂血症,动脉粥样硬化和其他与代谢紊乱有关的症状。方法为了评估FTZ对胰岛素抵抗的影响,以高胰岛素诱导的HepG2细胞作为胰岛素抵抗的模型,并以三种剂量之一的FTZ处理。接下来,测量葡萄糖含量,胰岛素受体底物1(IRS1)蛋白表达和磷脂酰肌醇3-激酶(PI3K)亚基p85 mRNA表达的水平。或者,通过强饲高脂饮食连续四周诱导大鼠MS,然后连续八周给予FTZ。评估体重,血浆脂质,胰岛素和葡萄糖水平。最后,测定了大鼠脂肪组织中PI3K p85 mRNA的表达。结果我们的结果显示,FTZ在体外可降低胰岛素抵抗性HepG2细胞中的葡萄糖含量并上调PI3K p85 mRNA和IRS1蛋白的表达。此外,FTZ降低了胰岛素抵抗性MS大鼠的体重和血浆三酰甘油,胆固醇,空腹血糖和胰岛素的浓度。 FTZ还提高了MS大​​鼠脂肪组织中PI3K p85 mRNA的表达。结论FTZ通过降低血浆葡萄糖和脂质水平减轻了MS症状。其潜在机制是减轻胰岛素抵抗的HepG 2 细胞和MS大鼠PI3K p85 mRNA和IRS1蛋白表达的降低。

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