Modulation of methotrexate-induced intestinal mucosal injury by dietary factors

Author:

Higuchi T12,Yoshimura M12,Oka S134,Tanaka K5,Naito T5,Yuhara S6,Warabi E7,Mizuno S8,Ono M9,Takahashi S7,Tohma S34,Tsuchiya N1,Furukawa H134ORCID

Affiliation:

1. Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

2. Both the authors contributed equally to this work.

3. Clinical Research Center for Allergy and Rheumatology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan

4. Department of Rheumatology, National Hospital Organization Tokyo National Hospital, Kiyose, Japan

5. Business Department, Miraca Research Institute G.K., Sagamihara, Japan

6. Research Department, Miraca Research Institute G.K., Hachioji, Japan

7. Department of Anatomy and Embryology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

8. Laborarory Animal Resource Center, University of Tsukuba, Tsukuba, Japan

9. Department of Clinical Laboratory, National Hospital Organization Mito Medical Center, Ibaraki, Japan

Abstract

Methotrexate (MTX)-induced intestinal mucosal injury in animals has been studied to understand how MTX can cause gastrointestinal disorders, but the pathogenesis of gastrointestinal disorders is still uncertain. We have attempted to reveal how dietary factors influence intestinal toxicity due to MTX. Mice were fed normal chow (NC) or a high-fat high-sucrose diet (HFHSD) before oral administration of MTX. While MTX significantly decreased the survival rates of mice fed HFHSD, the intestinal epithelial injury was detected. MTX excretion in the feces of mice fed HFHSD was reduced. Change of diets between NC and HFHSD influences the survival. The survival rates of the mice fed a high-sucrose diet or control diet were higher than those fed HFHSD. Higher survival rates were observed in mice fed a high-fat high-sucrose diet modified (HFHSD-M) in which casein was replaced by soybean-derived proteins. The survival rates of mice treated with vancomycin were lower than those administered neomycin. Microbiome and metabolome analyses on feces suggest a similarity of the intestinal environments of mice fed NC and HFHSD-M. HFHSD may modify MTX-induced toxicity in intestinal epithelia on account of an altered MTX distribution as a result of change in the intestinal environment.

Funder

Takeda Science Foundation

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

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