Ketogenic Diet Protects from Experimental Colitis in a Mouse Model Regardless of Dietary Fat Source

Author:

Toivio Lotta12ORCID,Lindén Jere34ORCID,Lehto Markku567ORCID,Salmenkari Hanne567ORCID,Korpela Riitta12

Affiliation:

1. Department of Pharmacology, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland

2. Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland

3. Department of Veterinary Biosciences, Faculty of Veterinary Medicine, University of Helsinki, 00014 Helsinki, Finland

4. Finnish Centre for Laboratory Animal Pathology, Helsinki Institute of Life Science, University of Helsinki, 00014 Helsinki, Finland

5. Folkhälsan Institute of Genetics, Folkhälsan Research Center, 00290 Helsinki, Finland

6. Department of Nephrology, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland

7. Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland

Abstract

While ketogenic diets (KDs) may have potential as adjunct treatments for gastrointestinal diseases, there is little knowledge on how the fat source of these diets impacts intestinal health. The objective of this study was to investigate how the source of dietary fat of KD influences experimental colitis. We fed nine-week-old male C57BL/6J mice (n = 36) with a low-fat control diet or KD high either in saturated fatty acids (SFA-KD) or polyunsaturated linoleic acid (LA-KD) for four weeks and then induced colitis with dextran sodium sulfate (DSS). To compare the diets, we analyzed macroscopic and histological changes in the colon, intestinal permeability to fluorescein isothiocyanate−dextran (FITC–dextran), and the colonic expression of tight junction proteins and inflammatory markers. While the effects were more pronounced with LA-KD, both KDs markedly alleviated DSS-induced histological lesions. LA-KD prevented inflammation-related weight loss and the shortening of the colon, as well as preserved Il1b and Tnf expression at a healthy level. Despite no significant between-group differences in permeability to FITC–dextran, LA-KD mitigated changes in tight junction protein expression. Thus, KDs may have preventive potential against intestinal inflammation, with the level of the effect being dependent on the dietary fat source.

Funder

Finnish Cultural Foundation’s Kymenlaakso regional fund

Finnish Concordia Fund

Finska Läkaresällskapet

Mary and Georg C. Ehrnrooth’s Foundation

Wilhelm and Else Stockmann Foundation

Novo Nordisk Foundation

University of Helsinki

Publisher

MDPI AG

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