Long-Term Overconsumption of Fat and Sugar Causes a Partially Reversible Pre-inflammatory Bowel Disease State.

IBD-inflammatory bowel diseases colitis diet-induced gut homeostasis high-fat high-sucrose diet

Journal

Frontiers in nutrition
ISSN: 2296-861X
Titre abrégé: Front Nutr
Pays: Switzerland
ID NLM: 101642264

Informations de publication

Date de publication:
2021
Historique:
received: 14 08 2021
accepted: 22 10 2021
entrez: 6 12 2021
pubmed: 7 12 2021
medline: 7 12 2021
Statut: epublish

Résumé

Nutrition appears to be an important environmental factor involved in the onset of inflammatory bowel diseases (IBD) through yet poorly understood biological mechanisms. Most studies focused on fat content in high caloric diets, while refined sugars represent up to 40% of caloric intake within industrialized countries and contribute to the growing epidemics of inflammatory diseases. Herein we aim to better understand the impact of a high-fat-high-sucrose diet on intestinal homeostasis in healthy conditions and the subsequent colitis risk. We investigated the early events and the potential reversibility of high caloric diet-induced damage in mice before experimental colitis. C57BL/6 mice were fed with a high-fat or high-fat high-sucrose or control diet before experimental colitis. In healthy mice, a high-fat high-sucrose diet induces a pre-IBD state characterized by gut microbiota dysbiosis with a total depletion of bacteria belonging to Barnesiella that is associated with subclinical endoscopic lesions. An overall down-regulation of the colonic transcriptome converged with broadly decreased immune cell populations in the mesenteric lymph nodes leading to the inability to respond to tissue injury. Such

Identifiants

pubmed: 34869528
doi: 10.3389/fnut.2021.758518
pmc: PMC8637418
doi:

Types de publication

Journal Article

Langues

eng

Pagination

758518

Informations de copyright

Copyright © 2021 Arnone, Vallier, Hergalant, Chabot, Ndiaye, Moulin, Aignatoaei, Alberto, Louis, Boulard, Mayeur, Dreumont, Peuker, Strigli, Zeissig, Hansmannel, Chamaillard, Kökten and Peyrin-Biroulet.

Déclaration de conflit d'intérêts

LP-B reports personal fees from AbbVie, Janssen, Genentech, Ferring, Tillots, Pharmacosmos, Celltrion, Takeda, Boerhinger Ingelheim, Pfizer, Index Pharmaceuticals, Sandoz, Celgene, Biogen, Samsung Bioepis, Alma, Sterna, Nestle, Enterome, Allergan, MSD, Roche, Arena, Gilead, Hikma, Amgen, BMS, Vifor, Norgine; Mylan, Lilly, Fresenius Kabi, Oppilan Pharma, Sublimity Therapeutics, Applied Molecular Transport, OSE Immunotherapeutics, Enthera, Theravance; grants from Abbvie, MSD, Takeda; stock options: CTMA. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Djésia Arnone (D)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

Marie Vallier (M)

Section of Evolutionary Medicine, Institute for Experimental Medicine, Kiel University and Max Planck Institute for Evolutionary Biology, Plön, Germany.

Sébastien Hergalant (S)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

Caroline Chabot (C)

CHRU-Nancy, Pediatric Hepato-Gastroenterology and Nutrition Unit, Department of Child Medicine and Clinical Genetics, Inserm U1256, Université de Lorraine, Nancy, France.

Ndeye Coumba Ndiaye (NC)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

David Moulin (D)

IMoPA, UMR7365 CNRS-Université de Lorraine, CHRU de Nancy, Contrat d'interface, Nancy, France.

Anda-Maria Aignatoaei (AM)

Department of Anatomopathology, CHRU de Nancy, Nancy, France.

Jean-Marc Alberto (JM)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

Huguette Louis (H)

Department Inserm UMRS_1116 DCAC, Université de Lorraine, Nancy, France.
Cytometry Core Facility, UMS2008 IBSLor (CNRS-Université de Lorraine-INSERM), Campus Brabois-Santé, Nancy, France.

Olivier Boulard (O)

Laboratory of Cell Physiology, INSERM U1003, University of Lille, Lille, France.

Camille Mayeur (C)

Micalis Institute, INRAE, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.

Natacha Dreumont (N)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

Kenneth Peuker (K)

Center for Regenerative Therapies, Technische Universität (TU) Dresden, Dresden, Germany.
Department of Medicine I, University Medical Center Dresden, Technische Universität (TU) Dresden, Dresden, Germany.

Anne Strigli (A)

Center for Regenerative Therapies, Technische Universität (TU) Dresden, Dresden, Germany.
Department of Medicine I, University Medical Center Dresden, Technische Universität (TU) Dresden, Dresden, Germany.

Sebastian Zeissig (S)

Center for Regenerative Therapies, Technische Universität (TU) Dresden, Dresden, Germany.
Department of Medicine I, University Medical Center Dresden, Technische Universität (TU) Dresden, Dresden, Germany.

Franck Hansmannel (F)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

Matthias Chamaillard (M)

Laboratory of Cell Physiology, INSERM U1003, University of Lille, Lille, France.

Tunay Kökten (T)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.

Laurent Peyrin-Biroulet (L)

Inserm U1256, Nutrition Genetics and Exposition NGERE, Université de Lorraine, Nancy, France.
Department of Gastroenterology, CHRU-Nancy, Université de Lorraine, Nancy, France.

Classifications MeSH