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dc.contributor.authorYoo, Hye Hyun-
dc.contributor.authorLee, Mijin-
dc.contributor.authorLee, Min Woo-
dc.contributor.authorLim, Sun Young-
dc.contributor.authorShin, Jongheon-
dc.contributor.authorKim, Dong-Hyun-
dc.date.accessioned2024-01-21T01:03:42Z-
dc.date.available2024-01-21T01:03:42Z-
dc.date.created2021-09-02-
dc.date.issued2007-05-
dc.identifier.issn0032-0943-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/134428-
dc.description.abstractSchisandra fruits (Schisandraceae) are often used in traditional medicine and can be taken concomitantly with conventional medicine. In this study, the effects of dibenzocyclooctadiene lignans from Schizandra chinensis on P-gp-mediated efflux were examined to investigate a possible interaction with P-gp substrates. The cellular accumulation of rhodamine-123 in Caco-2 cells was measured with 12 Schisandra lignans. Most compounds resulted in slight or moderate increases of rhodamin-1 23 cellular uptake, indicating their P-gp inhibitory activity. Among them, cleoxyschizandrin exhibited the most potent effect on the accumulation of rhodamine-123. Subsequently, bidirectional transports of digoxin and rhodamine-123 in Caco-2 cells were determined with cleoxyschizandrin, the most active compound for the rhodamine-123 assay. In the bidirectional transport study, apical-to-basal (A-to-B) transports of digoxin and rhodamine- 123 were increased, whereas basal-to-apical (B-to-A) transports were decreased by deoxyschizandrin in concentration- and time-dependent manners. At 50 mu M of deoxyschizandrin, the transport ratios (B-A/A-B) for digoxin and rhodamine-123 were 2.2 and 2.1 compared with the control ratios of 15.2 and 12.2, respectively. These results demonstrated that deoxyschizandrin effectively inhibited the P-gp-mediated efflux in Caco-2 cells, suggesting they could potentially increase the absorption of drugs that can act as a P-gp substrate.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectGOMISIN-A-
dc.subjectDIBENZOCYCLOOCTADIENE LIGNANS-
dc.subjectANTIOXIDANT ACTIVITY-
dc.subjectHEPATOCARCINOGENESIS-
dc.subjectCYTOCHROME-P450-
dc.subjectMETABOLISM-
dc.subjectCHINENSIS-
dc.subjectTRANSPORT-
dc.subjectCYP3A4-
dc.subjectDIET-
dc.titleEffects of Schisandra lignans on P-glycoprotein-mediated drug efflux in human intestinal Caco-2 cells-
dc.typeArticle-
dc.identifier.doi10.1055/s-2007-967178-
dc.description.journalClass1-
dc.identifier.bibliographicCitationPLANTA MEDICA, v.73, no.5, pp.444 - 450-
dc.citation.titlePLANTA MEDICA-
dc.citation.volume73-
dc.citation.number5-
dc.citation.startPage444-
dc.citation.endPage450-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000246963300006-
dc.identifier.scopusid2-s2.0-34250365825-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryIntegrative & Complementary Medicine-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaIntegrative & Complementary Medicine-
dc.type.docTypeArticle-
dc.subject.keywordPlusGOMISIN-A-
dc.subject.keywordPlusDIBENZOCYCLOOCTADIENE LIGNANS-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordPlusHEPATOCARCINOGENESIS-
dc.subject.keywordPlusCYTOCHROME-P450-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusCHINENSIS-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusCYP3A4-
dc.subject.keywordPlusDIET-
dc.subject.keywordAuthorSchisandra chinensis-
dc.subject.keywordAuthorSchisandraceae-
dc.subject.keywordAuthorP-glycoprotein-
dc.subject.keywordAuthordibenzo-cyclooctadiene lignans-
dc.subject.keywordAuthordeoxyschizandrin-
dc.subject.keywordAuthorCaco-2 cells-
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