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Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease
Reshaping the intestinal microbiota by the ingestion of fiber, such as pectin, improves alcohol-induced liver lesions in mice by modulating bacterial metabolites, including indoles, as well as bile acids (BAs). In this context, we aimed to elucidate how oral supplementation of pectin affects BA meta...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946080/ https://www.ncbi.nlm.nih.gov/pubmed/35326419 http://dx.doi.org/10.3390/cells11060968 |
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author | Ciocan, Dragos Spatz, Madeleine Trainel, Nicolas Hardonnière, Kévin Domenichini, Séverine Mercier-Nomé, Françoise Desmons, Aurore Humbert, Lydie Durand, Sylvère Kroemer, Guido Lamazière, Antonin Hugot, Cindy Perlemuter, Gabriel Cassard, Anne-Marie |
author_facet | Ciocan, Dragos Spatz, Madeleine Trainel, Nicolas Hardonnière, Kévin Domenichini, Séverine Mercier-Nomé, Françoise Desmons, Aurore Humbert, Lydie Durand, Sylvère Kroemer, Guido Lamazière, Antonin Hugot, Cindy Perlemuter, Gabriel Cassard, Anne-Marie |
author_sort | Ciocan, Dragos |
collection | PubMed |
description | Reshaping the intestinal microbiota by the ingestion of fiber, such as pectin, improves alcohol-induced liver lesions in mice by modulating bacterial metabolites, including indoles, as well as bile acids (BAs). In this context, we aimed to elucidate how oral supplementation of pectin affects BA metabolism in alcohol-challenged mice receiving feces from patients with alcoholic hepatitis. Pectin reduced alcohol liver disease. This beneficial effect correlated with lower BA levels in the plasma and liver but higher levels in the caecum, suggesting that pectin stimulated BA excretion. Pectin modified the overall BA composition, favoring an augmentation in the proportion of hydrophilic forms in the liver, plasma, and gut. This effect was linked to an imbalance between hydrophobic and hydrophilic (less toxic) BAs in the gut. Pectin induced the enrichment of intestinal bacteria harboring genes that encode BA-metabolizing enzymes. The modulation of BA content by pectin inhibited farnesoid X receptor signaling in the ileum and the subsequent upregulation of Cyp7a1 in the liver. Despite an increase in BA synthesis, pectin reduced BA serum levels by promoting their intestinal excretion. In conclusion, pectin alleviates alcohol liver disease by modifying the BA cycle through effects on the intestinal microbiota and enhanced BA excretion. |
format | Online Article Text |
id | pubmed-8946080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89460802022-03-25 Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease Ciocan, Dragos Spatz, Madeleine Trainel, Nicolas Hardonnière, Kévin Domenichini, Séverine Mercier-Nomé, Françoise Desmons, Aurore Humbert, Lydie Durand, Sylvère Kroemer, Guido Lamazière, Antonin Hugot, Cindy Perlemuter, Gabriel Cassard, Anne-Marie Cells Article Reshaping the intestinal microbiota by the ingestion of fiber, such as pectin, improves alcohol-induced liver lesions in mice by modulating bacterial metabolites, including indoles, as well as bile acids (BAs). In this context, we aimed to elucidate how oral supplementation of pectin affects BA metabolism in alcohol-challenged mice receiving feces from patients with alcoholic hepatitis. Pectin reduced alcohol liver disease. This beneficial effect correlated with lower BA levels in the plasma and liver but higher levels in the caecum, suggesting that pectin stimulated BA excretion. Pectin modified the overall BA composition, favoring an augmentation in the proportion of hydrophilic forms in the liver, plasma, and gut. This effect was linked to an imbalance between hydrophobic and hydrophilic (less toxic) BAs in the gut. Pectin induced the enrichment of intestinal bacteria harboring genes that encode BA-metabolizing enzymes. The modulation of BA content by pectin inhibited farnesoid X receptor signaling in the ileum and the subsequent upregulation of Cyp7a1 in the liver. Despite an increase in BA synthesis, pectin reduced BA serum levels by promoting their intestinal excretion. In conclusion, pectin alleviates alcohol liver disease by modifying the BA cycle through effects on the intestinal microbiota and enhanced BA excretion. MDPI 2022-03-11 /pmc/articles/PMC8946080/ /pubmed/35326419 http://dx.doi.org/10.3390/cells11060968 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ciocan, Dragos Spatz, Madeleine Trainel, Nicolas Hardonnière, Kévin Domenichini, Séverine Mercier-Nomé, Françoise Desmons, Aurore Humbert, Lydie Durand, Sylvère Kroemer, Guido Lamazière, Antonin Hugot, Cindy Perlemuter, Gabriel Cassard, Anne-Marie Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease |
title | Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease |
title_full | Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease |
title_fullStr | Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease |
title_full_unstemmed | Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease |
title_short | Modulation of the Bile Acid Enterohepatic Cycle by Intestinal Microbiota Alleviates Alcohol Liver Disease |
title_sort | modulation of the bile acid enterohepatic cycle by intestinal microbiota alleviates alcohol liver disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946080/ https://www.ncbi.nlm.nih.gov/pubmed/35326419 http://dx.doi.org/10.3390/cells11060968 |
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