Tartary buckwheat flavonoids protect hepatic cells against high glucose-induced oxidative stress and insulin resistance via MAPK signaling pathways

被引:47
作者
Hu, Yuanyuan [1 ]
Hou, Zuoxu [2 ]
Liu, Dongyang [3 ]
Yang, Xingbin [1 ]
机构
[1] Shaanxi Normal Univ, Coll Food Engn & Nutr Sci, Xian 710062, Peoples R China
[2] Fourth Mil Med Univ, Dept Aerosp Med, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, Brigade Cadets 1, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; HEPG2; CELLS; EPIGALLOCATECHIN GALLATE; MOLECULAR-MECHANISMS; QUERCETIN; RUTIN; GLUTATHIONE; APOPTOSIS; ANTIOXIDANT; RECEPTOR;
D O I
10.1039/c5fo01467k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1523 / 1536
页数:14
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