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Tea polyphenols protect bovine mammary epithelial cells from hydrogen peroxide-induced oxidative damage in vitro

文献类型： 外文期刊

作者： Ma, Yanfen 1 ; Zhao, Lei 1 ; Gao, Min 1 ; Loor, Juan J. 2 ;

作者机构： 1.Inner Mongolia Acad Agr & Anim Husb Sci, Inst Anim Nutr & Feed, Hohhot 010031, Peoples R China

2.Univ Illinois, Dept Anim Sci, 328 Mumford Hall, Urbana, IL 61801 USA

3.Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA

关键词： bovine mammary epithelial cells; oxidative stress; tea polyphenols

期刊名称：JOURNAL OF ANIMAL SCIENCE （ 影响因子：3.159； 五年影响因子：2.912 ）

ISSN： 0021-8812

年卷期： 2018 年 96 卷 10 期

页码：

收录情况： SCI

摘要： Periparturient dairy cows are subjected to altered intracellular reduction-oxidation (redox) balance due to the high metabolic rates and physiological adaptations characteristic of the transition into lactation. Such conditions could alter oxidative stress status. The objective of this study was to investigate the cytoprotective effects of tea polyphenols (TP) in cultured bovine mammary epithelial cells (BMEC) exposed to hydrogen peroxide (H2O2)-induced oxidative stress. To establish oxidative stress, isolated BMEC were exposed to increasing concentrations of H2O2 (0, 100, 200, 400, 600, 800, and 1,000 mu M) for 0, 2, 4, 6, 8, 12, and 24 h. Doses of TP (0, 60, 80, and 100 mu g/mL) were evaluated by pretreatment of BMEC for 0, 2, 4, 6, 8, 12 and 24 h, followed by an H2O2 (600 mu M per culture well) challenge for 6 h. Bovine mammary epithelial cells were preincubated for 30 min with or without 2,4-dinitrochloro-benzene (DNCB), then cultured with or without TP (100 mu g/mL) for another 12 h followed by H2O2 (600 mu M per culture well) exposure. There were 5 replicate cultures for each treatment in each experiment. Treatment with 600 mu M H2O2 per culture well for 6 h induced oxidative damage of BMEC, indicating this system could be used to establish an oxidative stress model. After H2O2 (600 mu M per culture well) exposure, a concentration of TP of 100 mu g/mL during a 12-h incubation increased cell viability, decreased intracellular reactive oxygen species accumulation, and increased the abundance of nuclear factor-erythroid 2-related factor 2 (NFE2L2). Furthermore, TP upregulated mRNA abundance of genes in the NFE2L2 and mitogen-activated protein kinase (MAPK) pathways of BMEC. The DNCB assay allowed further confirmation that the induction of NFE2L2 and HMOX-1 in response to TP was mediated through the sustained upregulation of the abundance of MAPK3/1 [formerly known as extracellular regulated kinases 1/2] and MAPK11/12/13/14 (formerly known as p38). Overall, results indicate that TP has beneficial effects on BMEC redox balance; it can reduce cellular oxidative stress-related injury and may potentially serve as an antioxidant against oxidative stress in dairy cows.

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