Evaluation of Cross-Talk and Alleviate Potential of Cytotoxic Factors Induced by Deoxynivalenol in IPEC-J2 Cells Interference with Curcumin

被引:2
|
作者
Wang, Qiyuan [1 ,2 ]
Li, Aike [1 ]
Yu, Hao [2 ]
Wang, Chuanqi [2 ]
Wang, Ting [2 ]
Zhang, Jing [1 ]
机构
[1] Acad Natl Food & Strateg Reserves Adm, Beijing 100037, Peoples R China
[2] Jilin Univ, Coll Anim Sci, Changchun 130062, Peoples R China
基金
中国国家自然科学基金;
关键词
deoxynivalenol; curcumin; cross-talk; cytotoxic factors; IPEC-J2; cells; OXIDATIVE STRESS; TNF-ALPHA; BIOAVAILABILITY; APOPTOSIS; FEED; PHARMACOKINETICS; INFLAMMATION; SUPPRESSION; PERFORMANCE; INHIBITION;
D O I
10.3390/ijms25136984
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
Deoxynivalenol (DON) is a mycotoxin produced by Fusarium graminearum, and curcumin (CUR) is a natural polyphenolic compound found in turmeric. However, the combined treatment of CUR and DON to explore the mitigating effect of CUR on DON and their combined mechanism of action is not clear. Therefore, in this study, we established four treatment groups (CON, CUR, DON and CUR + DON) to investigate their mechanism in the porcine intestinal epithelial cells (IPEC-J2). In addition, the cross-talk and alleviating potential of CUR interfering with DON-induced cytotoxic factors were evaluated by in vitro experiments; the results showed that CUR could effectively inhibit DON-exposed activated TNF-alpha/NF-kappa B pathway, attenuate DON-induced apoptosis, and alleviate DON-induced endoplasmic reticulum stress and oxidative stress through PERK/CHOP pathways, which were verified at both mRNA and protein levels. In conclusion, these promising findings may contribute to the future use of CUR as a novel feed additive to protect livestock from the harmful effects of DON.
引用
收藏
页数:20
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