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Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota

The effects of dimethyl fumarate (DMF) on mycotoxins and animal growth performance are well documented. However, its mechanism of anti-mildew effects is still unknown. The current study investigated how DMF detoxified the mycotoxin and improved the growth performance using BALB/c mice model, especia...

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Autores principales: Ma, Ning, Wu, Yi, Xie, Fei, Du, Kexin, Wang, Yuan, Shi, Linxin, Ji, Linbao, Liu, Tianyi, Ma, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546506/
https://www.ncbi.nlm.nih.gov/pubmed/28574825
http://dx.doi.org/10.18632/oncotarget.17886
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author Ma, Ning
Wu, Yi
Xie, Fei
Du, Kexin
Wang, Yuan
Shi, Linxin
Ji, Linbao
Liu, Tianyi
Ma, Xi
author_facet Ma, Ning
Wu, Yi
Xie, Fei
Du, Kexin
Wang, Yuan
Shi, Linxin
Ji, Linbao
Liu, Tianyi
Ma, Xi
author_sort Ma, Ning
collection PubMed
description The effects of dimethyl fumarate (DMF) on mycotoxins and animal growth performance are well documented. However, its mechanism of anti-mildew effects is still unknown. The current study investigated how DMF detoxified the mycotoxin and improved the growth performance using BALB/c mice model, especially its effects on intestinal barrier function and gut micro-ecology. Our study also compared with the ultraviolet radiation (UR) treatment, a traditional anti-mildew control (TC). The results indicated that the DMF treatment had a lower contents of mycotoxin, better growth performance and improved mucosal morphology (P < 0.05), accompanied with the decreased intestinal permeability and the tighter gut barrier. Moreover, the efficiency of DMF was better than TC (P < 0.05). 16S rRNA gene sequence analysis revealed that the richness and diversity of bacteria was increased in DMF treatment. The most abundant OTUs belonged to Firmicutes and Bacteroidetes, and their changes in DMF were more moderate than the TC group, suggesting a more stable micro-ecology and the positive impact of DMF on the biodiversity of intestine. Specifically, the increased abundance of bacteria producing short-chain fatty acids (SCFAs), such as Gemella, Roseburia, Bacillus and Bacteroides in DMF group and prebiotics such as Lactobacillus in TC group, suggested a more healthier microbial composition and distribution. These findings supported that DMF had significant effects on animal's growth performance and intestinal barrier function by modulating the pathway of nutrient absorption and increasing the diversity and balance of gut microbes, which also illuminate that DMF is more efficient than traditional anti-mildew method.
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spelling pubmed-55465062017-08-23 Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota Ma, Ning Wu, Yi Xie, Fei Du, Kexin Wang, Yuan Shi, Linxin Ji, Linbao Liu, Tianyi Ma, Xi Oncotarget Research Paper The effects of dimethyl fumarate (DMF) on mycotoxins and animal growth performance are well documented. However, its mechanism of anti-mildew effects is still unknown. The current study investigated how DMF detoxified the mycotoxin and improved the growth performance using BALB/c mice model, especially its effects on intestinal barrier function and gut micro-ecology. Our study also compared with the ultraviolet radiation (UR) treatment, a traditional anti-mildew control (TC). The results indicated that the DMF treatment had a lower contents of mycotoxin, better growth performance and improved mucosal morphology (P < 0.05), accompanied with the decreased intestinal permeability and the tighter gut barrier. Moreover, the efficiency of DMF was better than TC (P < 0.05). 16S rRNA gene sequence analysis revealed that the richness and diversity of bacteria was increased in DMF treatment. The most abundant OTUs belonged to Firmicutes and Bacteroidetes, and their changes in DMF were more moderate than the TC group, suggesting a more stable micro-ecology and the positive impact of DMF on the biodiversity of intestine. Specifically, the increased abundance of bacteria producing short-chain fatty acids (SCFAs), such as Gemella, Roseburia, Bacillus and Bacteroides in DMF group and prebiotics such as Lactobacillus in TC group, suggested a more healthier microbial composition and distribution. These findings supported that DMF had significant effects on animal's growth performance and intestinal barrier function by modulating the pathway of nutrient absorption and increasing the diversity and balance of gut microbes, which also illuminate that DMF is more efficient than traditional anti-mildew method. Impact Journals LLC 2017-05-16 /pmc/articles/PMC5546506/ /pubmed/28574825 http://dx.doi.org/10.18632/oncotarget.17886 Text en Copyright: © 2017 Ma et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ma, Ning
Wu, Yi
Xie, Fei
Du, Kexin
Wang, Yuan
Shi, Linxin
Ji, Linbao
Liu, Tianyi
Ma, Xi
Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
title Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
title_full Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
title_fullStr Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
title_full_unstemmed Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
title_short Dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
title_sort dimethyl fumarate reduces the risk of mycotoxins via improving intestinal barrier and microbiota
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546506/
https://www.ncbi.nlm.nih.gov/pubmed/28574825
http://dx.doi.org/10.18632/oncotarget.17886
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