Abstract

Non-steroidal anti-inflammatory drugs (NSAIDs) induce small intestinal damage. It has been reported that rebamipide, a mucoprotective drug, exerts a protective effect against NSAID-induced small intestinal damage; however, the underlying mechanism remains unknown. In this study, we investigated the significance of the small intestinal microbiota in the protective effect of rebamipide against indomethacin-induced small intestinal damage in mice. A comprehensive analysis of the 16S rRNA gene sequencing revealed an alteration in the composition of the small intestinal microbiota at the species level, modulated by the administration of rebamipide and omeprazole. The transplantation of the small intestinal microbiota of the mice treated with rebamipide suppressed the indomethacin-induced small intestinal damage. Omeprazole, a proton pump inhibitor, exacerbated the indomethacin-induced small intestinal damage, which was accompanied by the alteration of the small intestinal microbiota. We found that the transplantation of the small intestinal microbiota of the rebamipide-treated mice ameliorated indomethacin-induced small intestinal damage and the omeprazole-induced exacerbation of the damage. These results suggest that rebamipide exerts a protective effect against NSAID-induced small intestinal damage via the modulation of the small intestinal microbiota, and that its ameliorating effect extends also to the exacerbation of NSAID-induced small intestinal damage by proton pump inhibitors.

Highlights

  • We examined whether omeprazole exacerbate indomethacin-induced small intestinal damage in mice and whether it is suppressed by modulation of the small intestinal microbiota by rebamipide

  • These results suggest that the small intestinal microbiota modulated by rebamipide results in resistance to exacerbation of Non-steroidal anti-inflammatory drugs (NSAIDs)-induced small intestinal damage by pump inhibitors (PPIs)

  • Several studies suggest that the loss of microbial diversity in the gut microbiota is associated with some gastrointestinal diseases, such as Crohn’s disease [34], ulcerative colitis [35], irritable bowel syndrome [36], graft-versus-host disease in allogeneic hematopoietic-cell transplantation [37,38,39,40]

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Summary

Introduction

Rebamipide suppress indomethacin-induced small intestinal damage by modulation of small intestinal microbiota (https://figshare.com/articles/dataset/ Rebamipide_Suppress_Indomethacin-Induced_ Small_Intestinal_Damage_by_Modulation_of_ Small_Intestinal_Microbiota/13241267), DOI: 10. Rebamipide suppress indomethacin-induced small intestinal damage by modulation of small intestinal microbiota (https://figshare.com/articles/dataset/ Rebamipide_Suppress_Indomethacin-Induced_ Small_Intestinal_Damage_by_Modulation_of_ Small_Intestinal_Microbiota/13241267), DOI: 10. 6084/m9.figshare.13241267

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