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dc.contributor.author배옥남-
dc.date.accessioned2018-05-14T05:38:29Z-
dc.date.available2018-05-14T05:38:29Z-
dc.date.issued2016-12-
dc.identifier.citationBIOCHEMICAL PHARMACOLOGY, v. 122, Page. 72-79en_US
dc.identifier.issn0006-2952-
dc.identifier.issn1873-2968-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0006295216303069-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/71357-
dc.description.abstractIn this study, we investigated the effects of antibiotics on the pharmacological effects of aspirin. The antithrombotic activity of aspirin was evaluated after antibiotic treatment using tail bleeding assay. The pyrosequencing analysis and selective medium culture assay were performed to investigate the alterations in gut microbiota. In addition, the in vitro metabolism assay with fecal suspension and in vivo pharmacokinetic experiments with antibiotic treatment were conducted. Ampicillin treatment "significantly prolonged the bleeding time in aspirin-dosed rats. Oral administration of ampicillin significantly reduced gut microbial aspirin-metabolizing activity by 67.0% in rats. Furthermore, systemic exposure to aspirin and its primary metabolite (M1) was significantly increased in ampicillin-treated rats. The results from the pyrosequencing and selective medium culture with rat fecal samples revealed that ampicillin treatment led to the changes of the amounts and composition profile of gut microbiota. These findings suggest that co-administration of antibiotics can modulate the metabolism and pharmacokinetics of aspirin via suppression of metabolic activity of gut microbiota, which could potentiate the therapeutic potency of aspirin. (C) 2016 Elsevier Inc. All rights reserved.en_US
dc.description.sponsorshipThis work was supported by a grant from the Ministry of Food and Drug Safety in 2016 [16182MFDS416] and by a grant from the National Research Foundation of Korea [NRF-2014R1A1A1A05002840].en_US
dc.language.isoen_USen_US
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDen_US
dc.subjectAspirinen_US
dc.subjectAntithrombotic effecten_US
dc.subjectMetabolismen_US
dc.subjectAntibioticsen_US
dc.subjectGut microbiotaen_US
dc.subjectPERSONALIZED MEDICINEen_US
dc.subjectBIOAVAILABILITYen_US
dc.subjectXENOBIOTICSen_US
dc.subjectPROJECTen_US
dc.subjectDRUGSen_US
dc.subjectACIDen_US
dc.subjectRATSen_US
dc.titleReduced metabolic activity of gut microbiota by antibiotics can potentiate the antithrombotic effect of aspirinen_US
dc.typeArticleen_US
dc.relation.volume122-
dc.identifier.doi10.1016/j.bcp.2016.09.023-
dc.relation.page72-79-
dc.relation.journalBIOCHEMICAL PHARMACOLOGY-
dc.contributor.googleauthorKim, In Sook-
dc.contributor.googleauthorYoo, Dae-Hyeong-
dc.contributor.googleauthorJung, Il-Hoon-
dc.contributor.googleauthorLim, Sumin-
dc.contributor.googleauthorJeong, Jin-Ju-
dc.contributor.googleauthorKim, Kyeong-A-
dc.contributor.googleauthorBae, Ok-Nam-
dc.contributor.googleauthorYoo, Hye Hyun-
dc.contributor.googleauthorKim, Dong-Hyun-
dc.relation.code2016000808-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidonbae-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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