Gut Microbiota Reshaped by Pectin Treatment Improves Liver Steatosis in Obese Mice.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
22 Oct 2021
Historique:
received: 08 09 2021
revised: 12 10 2021
accepted: 20 10 2021
entrez: 27 11 2021
pubmed: 28 11 2021
medline: 15 12 2021
Statut: epublish

Résumé

Pectin, a soluble fiber, improves non-alcoholic fatty-liver disease (NAFLD), but its mechanisms are unclear. We aimed to investigate the role of pectin-induced changes in intestinal microbiota (IM) in NAFLD. We recovered the IM from mice fed a high-fat diet, treated or not with pectin, to perform a fecal microbiota transfer (FMT). Mice fed a high-fat diet, which induces NAFLD, were treated with pectin or received a fecal microbiota transfer (FMT) from mice treated with pectin before (preventive FMT) or after (curative FMT) being fed a high-fat diet. Pectin prevented the development of NAFLD, induced browning of adipose tissue, and modified the IM without increasing the abundance of proteobacteria. Preventive FMT also induced browning of white adipose tissue but did not improve liver steatosis, in contrast to curative FMT, which induced an improvement in steatosis. This was associated with an increase in the concentration of short-chain fatty acids (SCFAs), in contrast to preventive FMT, which induced an increase in the concentration of branched SCFAs. Overall, we show that the effect of pectin may be partially mediated by gut bacteria.

Identifiants

pubmed: 34835981
pii: nu13113725
doi: 10.3390/nu13113725
pmc: PMC8621973
pii:
doi:

Substances chimiques

Pectins 89NA02M4RX

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Servier (France)
ID : CT0069291-01
Organisme : Fondation pour la Recherche Médicale
ID : DEQ-20170336743

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Auteurs

Camille Houron (C)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.

Dragos Ciocan (D)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.
AP-HP, Hepato-Gastroenterology and Nutrition, Hôpital Antoine-Béclère, 92140 Clamart, France.

Nicolas Trainel (N)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.

Françoise Mercier-Nomé (F)

Université Paris-Saclay, Inserm, CNRS, Institut Paris Saclay d'Innovation Thérapeutique, 5 rue J.B. Clément, 92296 Châtenay-Malabry, France.

Cindy Hugot (C)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.

Madeleine Spatz (M)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.

Gabriel Perlemuter (G)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.
AP-HP, Hepato-Gastroenterology and Nutrition, Hôpital Antoine-Béclère, 92140 Clamart, France.

Anne-Marie Cassard (AM)

Université Paris-Saclay, Inserm U996, Inflammation, Microbiome and Immunosurveillance, 32 rue des carnets, 92140 Clamart, France.

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Classifications MeSH