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Dietary Lycium barbarum Polysaccharide Induces Nrf2/ARE Pathway and Ameliorates Insulin Resistance Induced by High-Fat via Activation of PI3K/AKT Signaling

机译:膳食枸杞多糖诱导Nrf2 / ARE途径并通过激活PI3K / AKT信号改善高脂诱导的胰岛素抵抗

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摘要

Lycium barbarum polysaccharide (LBP), an antioxidant from wolfberry, displays the antioxidative and anti-inflammatory effects on experimental models of insulin resistance in vivo. However, the effective mechanism of LBP on high-fat diet-induced insulin resistance is still unknown. The objective of the study was to investigate the mechanism involved in LBP-mediated phosphatidylinositol 3-kinase (PI3K)/AKT/Nrf2 axis against high-fat-induced insulin resistance. HepG2 cells were incubated with LBP for 12 hrs in the presence of palmitate. C57BL/6J mice were fed a high-fat diet supplemented with LBP for 24 weeks. We analyzed the expression of nuclear factor-E2-related factor 2 (Nrf2), Jun N-terminal kinases (JNK), and glycogen synthase kinase 3β (GSK3β) involved in insulin signaling pathway in vivo and in vitro. First, LBP significantly induced phosphorylation of Nrf2 through PI3K/AKT signaling. Second, LBP obviously increased detoxification and antioxidant enzymes expression and reduced reactive oxygen species (ROS) levels via PI3K/AKT/Nrf2 axis. Third, LBP also regulated phosphorylation levels of GSK3β and JNK through PI3K/AKT signaling. Finally, LBP significantly reversed glycolytic and gluconeogenic genes expression via the activation of Nrf2-mediated cytoprotective effects. In summary, LBP is novel antioxidant against insulin resistance induced by high-fat diet via activation of PI3K/AKT/Nrf2 pathway.
机译:枸杞的抗氧化剂枸杞多糖(LBP)对体内胰岛素抵抗的实验模型具有抗氧化和抗炎作用。但是,LBP对高脂饮食诱导的胰岛素抵抗的有效机制仍是未知的。该研究的目的是研究参与LBP介导的磷脂酰肌醇3-激酶(PI3K)/ AKT / Nrf2轴对抗高脂诱导的胰岛素抵抗的机制。在棕榈酸酯存在的情况下,将HepG2细胞与LBP孵育12小时。给C57BL / 6J小鼠喂食补充LBP的高脂饮食24周。我们分析了参与体内和体外胰岛素信号通路的核因子-E2相关因子2(Nrf2),Jun N末端激酶(JNK)和糖原合酶激酶3β(GSK3β)的表达。首先,LBP通过PI3K / AKT信号传导显着诱导Nrf2磷酸化。其次,LBP通过PI3K / AKT / Nrf2轴明显增加了排毒和抗氧化酶的表达,并降低了活性氧(ROS)的水平。第三,LBP还通过PI3K / AKT信号传导调节GSK3β和JNK的磷酸化水平。最后,LBP通过激活Nrf2介导的细胞保护作用,显着逆转了糖酵解和糖异生基因的表达。总之,LBP是一种通过激活PI3K / AKT / Nrf2途径抵抗高脂饮食诱导的胰岛素抵抗的新型抗氧化剂。

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