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Ginkgo biloba leaf extract suppresses intestinal human breast cancer resistance protein expression in mice: Correlation with gut microbiotaopen access

Authors
Kim, Jeon-KyungChoi, Min SunKim, Jae-YoungYu, Jun SangSeo, Jeong InYoo, Hye HyunKim, Dong-Hyun
Issue Date
Aug-2021
Publisher
Elsevier Masson
Keywords
BCRP; Drug transporter; Ginkgo biloba leaf extract; Gut microbiota; Herb-drug interaction
Citation
Biomedicine and Pharmacotherapy, v.140, pp 1 - 12
Pages
12
Indexed
SCIE
SCOPUS
Journal Title
Biomedicine and Pharmacotherapy
Volume
140
Start Page
1
End Page
12
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/105770
DOI
10.1016/j.biopha.2021.111712
ISSN
0753-3322
1950-6007
Abstract
In this study, we investigated the effects of treatment with Gingko biloba leaf extract (GLE) on intestinal transporter expression and gut microbiota composition in mice and the correlation between intestinal transporter expression and gut microbiota composition in mice. When GLE was orally administered to mice, intestinal BCRP expression was significantly suppressed. Pharmacokinetic studies showed that the maximum plasma concentration and area under the curve values of sulfasalazine were increased more than twice by treatment with GLE compared with those in the control group. GLE treatment significantly decreased the populations of Proteobacteria and Deferribacteres at the phylum level. Correlation analysis showed that BCRP expression was positively or negatively correlated with the composition of gut bacteria. In Caco-2 cells, GLE treatment did not affect BCRP expression, but treatment with the lysates of GLE-treated mouse feces significantly suppressed BCRP expression. These findings demonstrate that the suppression of intestinal BCRP expression following GLE treatment may occur through modulation of the gut microbiota composition. Thus, the present study suggests that modulation of gut microbiota composition may cause drug transporter-mediated herb–drug interactions. © 2021 The Authors
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