| Literature DB >> 33507971 |
Tetsuya Tanigawa1,2, Toshio Watanabe1, Akira Higashimori1, Sunao Shimada1,2, Hiroyuki Kitamura1, Takuya Kuzumoto1, Yuji Nadatani1, Koji Otani1, Shusei Fukunaga1, Shuhei Hosomi1, Fumio Tanaka1, Noriko Kamata1, Yasuaki Nagami1, Koichi Taira1, Masatsugu Shiba1, Wataru Suda3, Masahira Hattori3, Yasuhiro Fujiwara1.
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.Entities:
Year: 2021 PMID: 33507971 PMCID: PMC7842908 DOI: 10.1371/journal.pone.0245995
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240