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Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward
BACKGROUND: Excessive hedonic consumption is one of the main drivers for weight gain. Identifying contributors of this dysregulation would help to tackle obesity. The gut microbiome is altered during obesity and regulates host metabolism including food intake. RESULTS: By using fecal material transp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142783/ https://www.ncbi.nlm.nih.gov/pubmed/37106463 http://dx.doi.org/10.1186/s40168-023-01526-w |
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author | de Wouters d’Oplinter, Alice Verce, Marko Huwart, Sabrina J. P. Lessard-Lord, Jacob Depommier, Clara Van Hul, Matthias Desjardins, Yves Cani, Patrice D. Everard, Amandine |
author_facet | de Wouters d’Oplinter, Alice Verce, Marko Huwart, Sabrina J. P. Lessard-Lord, Jacob Depommier, Clara Van Hul, Matthias Desjardins, Yves Cani, Patrice D. Everard, Amandine |
author_sort | de Wouters d’Oplinter, Alice |
collection | PubMed |
description | BACKGROUND: Excessive hedonic consumption is one of the main drivers for weight gain. Identifying contributors of this dysregulation would help to tackle obesity. The gut microbiome is altered during obesity and regulates host metabolism including food intake. RESULTS: By using fecal material transplantation (FMT) from lean or obese mice into recipient mice, we demonstrated that gut microbes play a role in the regulation of food reward (i.e., wanting and learning processes associated with hedonic food intake) and could be responsible for excessive motivation to obtain sucrose pellets and alterations in dopaminergic and opioid markers in reward-related brain areas. Through untargeted metabolomic approach, we identified the 3-(3’-hydroxyphenyl)propanoic acid (33HPP) as highly positively correlated with the motivation. By administrating 33HPP in mice, we revealed its effects on food reward. CONCLUSIONS: Our data suggest that targeting the gut microbiota and its metabolites would be an interesting therapeutic strategy for compulsive eating, preventing inappropriate hedonic food intake. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01526-w. |
format | Online Article Text |
id | pubmed-10142783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101427832023-04-29 Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward de Wouters d’Oplinter, Alice Verce, Marko Huwart, Sabrina J. P. Lessard-Lord, Jacob Depommier, Clara Van Hul, Matthias Desjardins, Yves Cani, Patrice D. Everard, Amandine Microbiome Research BACKGROUND: Excessive hedonic consumption is one of the main drivers for weight gain. Identifying contributors of this dysregulation would help to tackle obesity. The gut microbiome is altered during obesity and regulates host metabolism including food intake. RESULTS: By using fecal material transplantation (FMT) from lean or obese mice into recipient mice, we demonstrated that gut microbes play a role in the regulation of food reward (i.e., wanting and learning processes associated with hedonic food intake) and could be responsible for excessive motivation to obtain sucrose pellets and alterations in dopaminergic and opioid markers in reward-related brain areas. Through untargeted metabolomic approach, we identified the 3-(3’-hydroxyphenyl)propanoic acid (33HPP) as highly positively correlated with the motivation. By administrating 33HPP in mice, we revealed its effects on food reward. CONCLUSIONS: Our data suggest that targeting the gut microbiota and its metabolites would be an interesting therapeutic strategy for compulsive eating, preventing inappropriate hedonic food intake. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01526-w. BioMed Central 2023-04-28 /pmc/articles/PMC10142783/ /pubmed/37106463 http://dx.doi.org/10.1186/s40168-023-01526-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research de Wouters d’Oplinter, Alice Verce, Marko Huwart, Sabrina J. P. Lessard-Lord, Jacob Depommier, Clara Van Hul, Matthias Desjardins, Yves Cani, Patrice D. Everard, Amandine Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
title | Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
title_full | Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
title_fullStr | Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
title_full_unstemmed | Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
title_short | Obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
title_sort | obese-associated gut microbes and derived phenolic metabolite as mediators of excessive motivation for food reward |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142783/ https://www.ncbi.nlm.nih.gov/pubmed/37106463 http://dx.doi.org/10.1186/s40168-023-01526-w |
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