Roles of stress response-related signaling and its contribution to the toxicity of zearalenone in mammals

被引:29
作者
Bai, Jun [1 ]
Zhou, Yusong [1 ]
Luo, Xin [1 ]
Hai, Jia [1 ]
Si, Xuemeng [1 ]
Li, Jun [1 ]
Fu, Huiyang [1 ]
Dai, Zhaolai [1 ]
Yang, Ying [1 ]
Wu, Zhenlong [1 ,2 ]
机构
[1] China Agr Univ, Dept Compan Anim Sci, Coll Anim Sci & Technol, State Key Lab Anim Nutr, Beijing, Peoples R China
[2] Beijing Jingwa Agr Sci & Technol Innovat Ctr, 1 Yuda Rd, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Endoplasmic reticulum stress; Oxidative stress; Toxicity; Zearalenone; ENDOPLASMIC-RETICULUM STRESS; GERM-CELL APOPTOSIS; MOUSE LEYDIG-CELLS; OXIDATIVE STRESS; BETA-ZEARALENOL; ER STRESS; MYCOTOXINS OCCURRENCE; NATURAL OCCURRENCE; ESTROGENIC MYCOTOXIN; DEOXYNIVALENOL DON;
D O I
10.1111/1541-4337.12974
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Zearalenone (ZEA) is a mycotoxin frequently found in cereal crops and cereal-derived foodstuffs worldwide. It affects plant productivity, and is also a serious hazard to humans and animals if being exposed to food/feed contaminated by ZEA. Studies over the last decade have shown that the toxicity of ZEA in animals is mainly mediated by the various stress responses, such as endoplasmic reticulum (ER) stress, oxidative stress, and others. Accumulating evidence shows that oxidative stress and ER stress signaling are actively implicated in and contributes to the pathophysiology of various diseases. Biochemically, the deleterious effects of ZEA are associated with apoptosis, DNA damage, and lipid peroxidation by regulating the expression of genes implicated in these biological processes. Despite these findings, the underlying mechanisms responsible for these alterations remain unclear. This review summarized the characteristics, metabolism, toxicity and the deleterious effects of ZEA exposure in various tissues of animals. Stress response signaling implicated in the toxicity as well as potential therapeutic options with the ability to reduce the deleterious effects of ZEA in animals were highlighted and discussed.
引用
收藏
页码:3326 / 3345
页数:20
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