董悦生

个人信息Personal Information

副教授

博士生导师

硕士生导师

性别:男

毕业院校:中国协和医科大学

学位:博士

所在单位:生物工程学院

学科:生物化工. 微生物学. 微生物与生化药学

办公地点:辽宁省大连市高新园区凌工路2号大连理工大学西部校区生物工程学院309室

联系方式:辽宁省大连市高新园区凌工路2号大连理工大学生物工程学院

电子邮箱:yshdong@dlut.edu.cn

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Baicalein Alleviates Liver Oxidative Stress and Apoptosis Induced by High-Level Glucose through the Activation of the PERK/Nrf2 Signaling Pathway

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论文类型:期刊论文

发表时间:2021-02-25

发表刊物:MOLECULES

卷号:25

期号:3

关键字:diabetes mellitus; baicalein; oxidative stress; apoptosis; liver; PERK/Nrf2 signaling pathway

摘要:Baicalein, a widely-distributed natural flavonoid, exhibits antioxidative activity in mice with type-2 diabetes. However, the underlying mechanisms remain partially elucidated. In this study, we investigated the effect of baicalein on protein kinase R-like ER kinase (PERK)/nuclear factor erythroid-2-related factor 2 (Nrf2) pathway for the alleviation of oxidative stress and apoptosis. Human liver HL-7702 cells were stimulated with 60.5 mM of glucose to induce oxidative stress and treated with baicalein. The apoptosis was determined by fluorescence microscopy and flow cytometry. The regulation of the PERK/Nrf2 pathway by baicalein was determined by immunoblotting in both HL-7702 cells and liver tissues from diabetic mice. We found that baicalein significantly alleviated the oxidative stress and apoptosis in HL-7702 cells stimulated with glucose. Mechanistic studies showed that baicalein downregulated PERK and upregulated Nrf2, two key proteins involved in endoplasmic reticulum stress, in both HL-7702 cells and liver tissues from diabetic mice receiving baicalein treatment. Furthermore, the subcellular localization of Nrf2 and the regulation of downstream proteins including heme oxygenase-1 and CCAAT-enhancer-binding protein homologous protein (CHOP) by baicalein were also investigated. Our results suggest that the regulation of the PERK/Nrf2 pathway is one of the mechanisms contributing to the bioactivities of baicalein to improve diabetes-associated complications.