The protective role of resveratrol against high glucose-induced oxidative stress and apoptosis in HepG2 cells

被引:6
作者
Tshivhase, Abegail Mukhethwa [1 ]
Matsha, Tandi [1 ,2 ]
Raghubeer, Shanel [1 ]
机构
[1] Cape Peninsula Univ Technol, Fac Hlth & Wellness Sci, Dept Biomed Sci, SAMRC CPUT Cardiometab Hlth Res Unit, ZA-7530 Bellville, South Africa
[2] Sefako Makgatho Hlth Sci Univ, Ga Rankuwa, South Africa
基金
新加坡国家研究基金会;
关键词
apoptosis; high glucose; hyperglycemia; oxidative stress; resveratrol; HIGH-FAT DIET; INSULIN-RESISTANCE; ACTIVATION; EXPRESSION; DAMAGE; MITOCHONDRIA; MECHANISM; RADICALS; ENZYME; LEADS;
D O I
10.1002/fsn3.4027
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
High glucose concentrations result in oxidative stress, leading to damage of cellular constituents like DNA, proteins, and lipids, ultimately resulting in apoptosis. Resveratrol, a polyphenol phytoalexin, has been studied for its potential therapeutic effects on diabetes. This study investigated the influence of high glucose (HG) on HepG2 cells and assessed resveratrol's effect on high-glucose-induced oxidative stress and apoptosis. HepG2 cells were cultured for 48 and 72 h with high glucose (40 mM), low resveratrol (25 mu M), high resveratrol (50 mu M), high glucose + low resveratrol, and high glucose + high resveratrol. After exposure, oxidative and apoptosis-related gene expression was evaluated using quantitative polymerase chain reaction (qPCR), and lactate dehydrogenase (LDH) release was measured using the supernatant. In HepG2 cells cultured with high glucose, all antioxidant enzymes (SOD, superoxide dismutase; GPx1, glutathione peroxidase 1; CAT, catalase; Nrf2, nuclear factor erythroid 2-related factor 2; and NQO1, NAD(P)H quinone oxidoreductase 1) were significantly reduced; however, when HepG2 cells were cultured with resveratrol (25 and 50 mu M) and high glucose, the expression levels of all antioxidant enzymes were increased. The anti-apoptotic gene (B-cell lymphoma 2; Bcl2) and the DNA repair gene (Oxoguanine glycosylase-1, OGG1) were significantly decreased following high glucose exposure to HepG2 cells. Surprisingly, the expression levels of Bcl2 and OGG1 were notably elevated after resveratrol treatment. Furthermore, high glucose levels increased the LHD release in HepG2 cells, whereas resveratrol treatment reduced the LDH release. Our results demonstrate that resveratrol provides protection against oxidative stress and apoptosis induced by high glucose in HepG2 cells. Hence, resveratrol shows potential as an effective approach to address the impaired antioxidant response resulting from elevated glucose levels commonly observed in diabetes and metabolic disorders. Our investigation into the effects of resveratrol on HepG2 cells demonstrates that resveratrol protects against high glucose-induced oxidative stress and apoptosis in HepG2 cells. Therefore, resveratrol may serve as a promising strategy to combat antioxidant response dysfunction caused by high glucose levels characteristic of diabetes conditions and metabolic disorders.image
引用
收藏
页码:3574 / 3584
页数:11
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