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首页> 外文期刊>Current topics in nutraceutical research >SOLUBLE DIETARY FIBER FROM FERMENTED SOYBEAN DREGS ENHANCES GLUCOSE UPTAKE AND MITIGATES INSULIN RESISTANCE IN HUMAN LIVER CANCER CELL (HEPG2) MODEL VIA AMPK/SIRT1 SIGNAL PATHWAY
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SOLUBLE DIETARY FIBER FROM FERMENTED SOYBEAN DREGS ENHANCES GLUCOSE UPTAKE AND MITIGATES INSULIN RESISTANCE IN HUMAN LIVER CANCER CELL (HEPG2) MODEL VIA AMPK/SIRT1 SIGNAL PATHWAY

机译:来自发酵大豆渣的可溶性膳食纤维增强了葡萄糖摄取和通过AMPK / SIRT1信号通路的人肝癌细胞(HepG2)模型中的胰岛素抵抗力

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In order to explore glucose uptake and elucidate the underlying mechanism of insulin resistance (IR) in human liver cancer cell (HepG2) upon the intervention of soluble dieta?) , fiber (SDF) from fermented soybean dregs, HepG2 cell model with insulin resistance (HepG2/IR) was established to measure the cell viability and glucose uptake by cholecystokinin (CCK) 8 and glucose oxidase (GOD) kits upon SDF intervention. Meanwhile, protein expression of insulin receptor substrate 1 (IRS-1) and protein kinase B (Akt) in HepG2/IR cells treated with SDF was evaluated by Western blot. Moreover, protein expression of Mfn2 and Drpl associated with mitochondrial dynamics in HepG2/IR cells exposed to SDF was detected Our results revealed that SDF increased glucose uptake in HepG2/IR cells, with evidences of up-regulated p-IRS, Akt, p-adenosine, 5'-monophosphate-activated protein kinase (AMPK), silent information regulator 1 (SIRT1) and irisin. Furthermore, SDF restored the balance of mitochondrial dynamics via up-regulating Mfn2, and down-regulating PGC-l alpha and Drpl in insulin-resistant HepG2 cells. In contrast, after blocking SIRT1 by EX527, the glucose uptake of HepG2/IR cells could not be rescued when treated with SDF. Therefore, SDF can mitigate or rescue insulin resistance to improve glucose uptake via regulating AMPK/SIRT1 signal pathway.
机译:为了探索葡萄糖摄取并阐明人肝癌细胞(Hepg2)的胰岛素抵抗(IR)的潜在机制在可溶性饮食的干预后,来自发酵大豆渣的纤维(SDF),HepG2细胞模型具有胰岛素抵抗(建立了HepG2 / IR)以测量细胞活力和通过胆囊蛋白(CCK)8和葡萄糖氧化酶(上帝)试剂盒在SDF干预时测量细胞活力和葡萄糖摄取。同时,通过蛋白质印迹评估用SDF处理的HepG2 / IR细胞中胰岛素受体基质1(IRS-1)和蛋白激酶B(Akt)的蛋白质表达。此外,检测到与暴露于SDF的HepG2 / IR细胞中的MFN2和与线粒体动态相关的MFN2和DRPL的蛋白表达显示,我们的结果表明,SDF增加了HepG2 / IR细胞中的葡萄糖摄取,具有上调的P-IRS,AKT,P-腺苷,5'-单磷酸活化的蛋白激酶(AMPK),无声信息调节器1(SIRT1)和Irisin。此外,SDF通过UP调节MFN2和胰岛素抗性HepG2细胞中的下调PGC-Lα和DRPL恢复线粒体动力学的平衡。相反,在通过EX527封闭SIRT1之后,在用SDF处理时不能拯救HepG2 / IR细胞的葡萄糖摄取。因此,SDF可以减轻或拯救胰岛素抵抗,以通过调节AMPK / SIRT1信号途径来改善葡萄糖摄取。

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