Deoxynivalenol Exposure Induced Colon Damage in Mice Independent of the Gut Microbiota

被引:3
作者
Liao, Yuxiao [1 ,2 ]
Peng, Zhao [1 ,2 ]
Xu, Shiyin [1 ,2 ]
Meng, Zitong [1 ,2 ]
Li, Dan [1 ,2 ]
Zhou, Xiaolei [1 ,2 ]
Zhang, Rui [3 ]
Shi, Shaojun [3 ,4 ]
Hao, Liping [1 ,2 ]
Liu, Liegang [1 ,2 ]
Yang, Wei [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Nutr & Food Hyg, Hubei Key Lab Food Nutr & Safety, Hangkong Rd 13, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Dept Nutr & Food Hyg, Hangkong Rd 13, Wuhan 430030, Peoples R China
[3] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pharm, Wuhan 430022, Peoples R China
[4] Huazhong Univ Sci & Technol, Union Jiangnan Hosp, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
colon damage; deoxynivalenol; fecal microbiota transplantation; gut microbiota; metabolites; INTESTINAL INFLAMMATION; CELL PROLIFERATION; INDUCED APOPTOSIS; OXIDATIVE STRESS; BARRIER; METABOLISM; INGESTION;
D O I
10.1002/mnfr.202300317
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope: To investigate whether deoxynivalenol (DON) can induce intestinal damage through gut microbiota in mice. Methods and results: Mice are orally administered DON (1 mg kg(-1) bw day(-1)) for 4 weeks, and then recipient mice receive fecal microbiota transplantation (FMT) from DON-exposed mice after antibiotic treatment. Furthermore, the mice are orally treated with DON (1 mg kg(-1) bw day(-1)) for 4 weeks after antibiotic treatment. Histological damage, disruption of tight junction protein expression, and increased oxidative stress and apoptosis in the colon as well as higher serum lipopolysaccharides are observed after DON exposure. Moreover, DON exposure changes the composition and diversity of the gut microbiota as well as the contents of fecal metabolites (mainly bile acids). Differential metabolic pathways may be related to mitochondrial metabolism, apoptosis, and inflammation following DON exposure. However, only a decrease in mRNA levels of occludin and claudin-3 is observed in the colon of recipient mice after FMT. After depleting the gut microbiota in mice, DON exposure can also cause histological damage, disorders of tight junction protein expression, and increased oxidative stress and apoptosis in the colon. Conclusions: DON exposure can induce colon damage in mice independent of the gut microbiota.
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页数:13
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