A murine model of pediatric inflammatory bowel disease causes microbiota-gut-brain axis deficits in adulthood

Author:

Salvo Eloisa1,Stokes Patricia1,Keogh Ciara E.1,Brust-Mascher Ingrid1,Hennessey Carly1,Knotts Trina A.2,Sladek Jessica A.1,Rude Kavi M.1,Swedek Michelle1,Rabasa Gonzalo1,Gareau Mélanie G.1ORCID

Affiliation:

1. Department of Anatomy, Physiology and Cell Biology, University of California, Davis, California

2. Department of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, California

Abstract

Here we describe long-lasting impacts on the microbiota-gut-brain (MGB) axis following administration of low-dose dextran sodium sulfate (DSS) to weaning mice (P21), including gut dysbiosis, colonic inflammation, and brain/behavioral deficits in adulthood (P56). Early-life DSS leads to acute colonic inflammation, similar to adult mice; however, it results in long-lasting deficits in the MGB axis in adulthood (P56), in contrast to the transient deficits seen in adult DSS. This model highlights the unique features of pediatric inflammatory bowel disease.

Funder

Crohn's and Colitis Foundation

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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