Protective Role of Hydrogen Gas on Oxidative Damage and Apoptosis in Intestinal Porcine Epithelial Cells (IPEC-J2) Induced by Deoxynivalenol: A Preliminary Study

被引:15
作者
Ji, Xu [1 ]
Zheng, Weijiang [1 ,2 ]
Yao, Wen [1 ,2 ,3 ]
机构
[1] Nanjing Agr Univ, Coll Anim Sci & Technol, Lab Gastrointestinal Microbiol, Jiangsu Key Lab Gastrointestinal Nutr & Anim Hlth, Nanjing 210095, Peoples R China
[2] Nanjing Agr Univ, Coll Anim Sci & Technol, Natl Expt Teaching Ctr Anim Sci, Nanjing 210095, Peoples R China
[3] Minist Agr, Key Lab Anim Physiol & Biochem, Nanjing 210095, Peoples R China
关键词
hydrogen gas; deoxynivalenol; IPEC-J2; oxidative damage; apoptosis; RICH MEDIUM; HIGH GLUCOSE; STRESS; CYTOTOXICITY; INJURY; METABOLISM; SALINE; DON; FIBROBLASTS; ANTIOXIDANT;
D O I
10.3390/toxins12010005
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
To explore the protective role of hydrogen gas (H-2) on oxidative damage and apoptosis in intestinal porcine epithelial cells (IPEC-J2) induced by deoxynivalenol (DON), cells were assigned to four treatment groups, including control, 5 mu M DON, H-2-saturated medium, and 5 mu M DON + H-2-saturated medium treatments. After 12 h of different treatments, the cell viability, biomarkers of cell redox states, and gene expression of antioxidant enzymes and apoptosis were observed and detected. Furthermore, caspase-3 and Bax protein expressions were measured by Western blot analysis. Our results demonstrated that the 5 mu M DON significantly caused cytotoxicity to IPEC-J2 cells by reducing cell viability and increasing lactate dehydrogenase release in culture supernatants. Moreover, DON treatments significantly increased levels of 8-hydroxy-2 '-deoxyguanosine, 3-nitrotyrosine, and malonaldehyde; however, they decreased total superoxide dismutase and catalase activities and downregulated messenger RNA (mRNA) expression related to antioxidant enzymes in cells. The 5 mu M DON treatment also downregulated Bcl-2 expression and upregulated caspase-3 and Bax expression. However, the H-2-saturated medium significantly improved cell growth status and reversed the change of redox states and expression of genes and proteins related to apoptosis induced by DON in IPEC-J2 cells. In conclusion, H-2 could protect IPEC-J2 cells from DON-induced oxidative damage and apoptosis in vitro.
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页数:14
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