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
相关论文
共 160 条
[91]   Self-eating and self-killing: crosstalk between autophagy and apoptosis [J].
Maiuri, M. Chiara ;
Zalckvar, Einat ;
Kimchi, Adi ;
Kroemer, Guido .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (09) :741-752
[92]   Species differences in the hepatic biotransformation of zearalenone [J].
Malekinejad, H. ;
Maas-Bakker, R. ;
Fink-Gremmels, J. .
VETERINARY JOURNAL, 2006, 172 (01) :96-102
[93]   Cytotoxic and inflammatory effects of individual and combined exposure of HepG2 cells to zearalenone and its metabolites [J].
Marin, D. E. ;
Pistol, G. C. ;
Bulgaru, C., V ;
Taranu, I .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2019, 392 (08) :937-947
[94]   Effects of zearalenone on oxidative stress and inflammation in weanling piglets [J].
Marin, Daniela E. ;
Pistol, Gina C. ;
Neagoe, Ionela V. ;
Calin, Loredana ;
Taranu, Ionelia .
FOOD AND CHEMICAL TOXICOLOGY, 2013, 58 :408-415
[95]   Effects of zearalenone and its derivatives on porcine immune response [J].
Marin, Daniela E. ;
Taranu, Ionelia ;
Burlacu, Radu ;
Manda, Gina ;
Motiu, Monica ;
Neagoe, Ionela ;
Dragomir, Catalin ;
Stancu, Mariana ;
Calin, Loredana .
TOXICOLOGY IN VITRO, 2011, 25 (08) :1981-1988
[96]   Mycotoxins: Occurrence, toxicology, and exposure assessment [J].
Marin, S. ;
Ramos, A. J. ;
Cano-Sancho, G. ;
Sanchis, V. .
FOOD AND CHEMICAL TOXICOLOGY, 2013, 60 :218-237
[97]   Oxidative degradation and detoxification of mycotoxins using a novel source of ozone [J].
McKenzie, KS ;
Sarr, AB ;
Mayura, K ;
Bailey, RH ;
Miller, DR ;
Rogers, TD ;
Norred, WP ;
Voss, KA ;
Plattner, RD ;
Kubena, LF ;
Phillips, TD .
FOOD AND CHEMICAL TOXICOLOGY, 1997, 35 (08) :807-820
[98]   Endoplasmic reticulum stress and the unfolded protein response in pancreatic islet inflammation [J].
Meyerovich, Kira ;
Ortis, Fernanda ;
Allagnat, Florent ;
Cardozo, Alessandra K. .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2016, 57 (01) :R1-R17
[99]   Zearalenone and Reproductive Function in Farm Animals [J].
Minervini, Fiorenza ;
Dell'Aquila, Maria Elena .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2008, 9 (12) :2570-2584
[100]   Animal Model Contributions to Congenital Metabolic Disease [J].
Moro, Corinna A. ;
Hanna-Rose, Wendy .
ANIMAL MODELS OF HUMAN BIRTH DEFECTS, 2020, 1236 :225-244