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Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota

BACKGROUND: Disruption of the gut microbiota homeostasis may induce low-grade inflammation leading to obesity-associated diseases. A major protective mechanism is to use the multi-layered mucus structures to keep a safe distance between gut epithelial cells and microbiota. To investigate whether pes...

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Autores principales: Liang, Yiran, Zhan, Jing, Liu, Donghui, Luo, Mai, Han, Jiajun, Liu, Xueke, Liu, Chang, Cheng, Zheng, Zhou, Zhiqiang, Wang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371608/
https://www.ncbi.nlm.nih.gov/pubmed/30744700
http://dx.doi.org/10.1186/s40168-019-0635-4
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author Liang, Yiran
Zhan, Jing
Liu, Donghui
Luo, Mai
Han, Jiajun
Liu, Xueke
Liu, Chang
Cheng, Zheng
Zhou, Zhiqiang
Wang, Peng
author_facet Liang, Yiran
Zhan, Jing
Liu, Donghui
Luo, Mai
Han, Jiajun
Liu, Xueke
Liu, Chang
Cheng, Zheng
Zhou, Zhiqiang
Wang, Peng
author_sort Liang, Yiran
collection PubMed
description BACKGROUND: Disruption of the gut microbiota homeostasis may induce low-grade inflammation leading to obesity-associated diseases. A major protective mechanism is to use the multi-layered mucus structures to keep a safe distance between gut epithelial cells and microbiota. To investigate whether pesticides would induce insulin resistance/obesity through interfering with mucus-bacterial interactions, we conducted a study to determine how long-term exposure to chlorpyrifos affected C57Bl/6 and CD-1 (ICR) mice fed high- or normal-fat diets. To further investigate the effects of chlorpyrifos-altered microbiota, antibiotic treatment and microbiota transplantation experiments were conducted. RESULTS: The results showed that chlorpyrifos caused broken integrity of the gut barrier, leading to increased lipopolysaccharide entry into the body and finally low-grade inflammation, while genetic background and diet pattern have limited influence on the chlorpyrifos-induced results. Moreover, the mice given chlorpyrifos-altered microbiota had gained more fat and lower insulin sensitivity. CONCLUSIONS: Our results suggest that widespread use of pesticides may contribute to the worldwide epidemic of inflammation-related diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0635-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-63716082019-02-25 Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota Liang, Yiran Zhan, Jing Liu, Donghui Luo, Mai Han, Jiajun Liu, Xueke Liu, Chang Cheng, Zheng Zhou, Zhiqiang Wang, Peng Microbiome Research BACKGROUND: Disruption of the gut microbiota homeostasis may induce low-grade inflammation leading to obesity-associated diseases. A major protective mechanism is to use the multi-layered mucus structures to keep a safe distance between gut epithelial cells and microbiota. To investigate whether pesticides would induce insulin resistance/obesity through interfering with mucus-bacterial interactions, we conducted a study to determine how long-term exposure to chlorpyrifos affected C57Bl/6 and CD-1 (ICR) mice fed high- or normal-fat diets. To further investigate the effects of chlorpyrifos-altered microbiota, antibiotic treatment and microbiota transplantation experiments were conducted. RESULTS: The results showed that chlorpyrifos caused broken integrity of the gut barrier, leading to increased lipopolysaccharide entry into the body and finally low-grade inflammation, while genetic background and diet pattern have limited influence on the chlorpyrifos-induced results. Moreover, the mice given chlorpyrifos-altered microbiota had gained more fat and lower insulin sensitivity. CONCLUSIONS: Our results suggest that widespread use of pesticides may contribute to the worldwide epidemic of inflammation-related diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0635-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-11 /pmc/articles/PMC6371608/ /pubmed/30744700 http://dx.doi.org/10.1186/s40168-019-0635-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liang, Yiran
Zhan, Jing
Liu, Donghui
Luo, Mai
Han, Jiajun
Liu, Xueke
Liu, Chang
Cheng, Zheng
Zhou, Zhiqiang
Wang, Peng
Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
title Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
title_full Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
title_fullStr Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
title_full_unstemmed Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
title_short Organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
title_sort organophosphorus pesticide chlorpyrifos intake promotes obesity and insulin resistance through impacting gut and gut microbiota
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371608/
https://www.ncbi.nlm.nih.gov/pubmed/30744700
http://dx.doi.org/10.1186/s40168-019-0635-4
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