Hu Yuanyuan, Hou Zuoxu, Liu Dongyang, Yang Xingbin
College of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi'an 710062, China.
Department of Aerospace Medicine, Fourth Military Medical University, Xi'an 710032, China.
Food Funct. 2016 Mar;7(3):1523-36. doi: 10.1039/c5fo01467k.
Oxidative stress plays a crucial role in chronic complication of diabetes. In this study, the protective effect of purified tartary buckwheat flavonoids (TBF) fraction against oxidative stress induced by a high-glucose challenge, which causes insulin resistance, was investigated on hepatic HepG2 cells. Oxidative status, phosphorylated mitogen-activated protein kinases (MAPKs), nuclear factor E2 related factor 2 (Nrf2) and p-(Ser307)-IRS-1 expression, and glucose uptake were evaluated. Results suggest that treatment of HepG2 cells with TBF alone improved glucose uptake and antioxidant enzymes, and activated Nrf2, and attenuated the IRS-1 Ser307 phosphorylation, and enhanced total levels of IRS-1. Furthermore, the high glucose-induced changes in antioxidant defences, Nrf2, p-MAPKs, p-IRS1 Ser307, and IRS-1 levels, and glucose uptake were also significantly inhibited by pre-treatment with TBF. Interestingly, the selective MAPK inhibitors significantly enhanced the TBF-mediated protection by inducing changes in the redox status, glucose uptake, p-(Ser307) and total IRS-1 levels. This report firstly showed that TBF could recover the redox status of insulin-resistant HepG2 cells, suggesting that TBF significantly protected the cells against high glucose-induced oxidative stress, and these beneficial effects of TBF on redox balance and insulin resistance were mediated by targeting MAPKs.
氧化应激在糖尿病慢性并发症中起关键作用。在本研究中,研究了纯化的苦荞黄酮(TBF)组分对高糖刺激诱导的氧化应激的保护作用,高糖刺激会导致胰岛素抵抗,该研究以肝HepG2细胞为对象。评估了氧化状态、磷酸化丝裂原活化蛋白激酶(MAPK)、核因子E2相关因子2(Nrf2)和p-(Ser307)-胰岛素受体底物-1(IRS-1)的表达以及葡萄糖摄取情况。结果表明,单独用TBF处理HepG2细胞可改善葡萄糖摄取和抗氧化酶,激活Nrf2,减弱IRS-1的Ser307磷酸化,并提高IRS-1的总水平。此外,TBF预处理也显著抑制了高糖诱导的抗氧化防御、Nrf2、磷酸化MAPK、p-IRS1 Ser307和IRS-1水平以及葡萄糖摄取的变化。有趣的是,选择性MAPK抑制剂通过诱导氧化还原状态、葡萄糖摄取、p-(Ser307)和总IRS-1水平的变化,显著增强了TBF介导的保护作用。本报告首次表明,TBF可以恢复胰岛素抵抗的HepG2细胞的氧化还原状态,这表明TBF能显著保护细胞免受高糖诱导的氧化应激,并且TBF对氧化还原平衡和胰岛素抵抗的这些有益作用是通过靶向MAPK介导的。