In vitro metabolism of Jaceosidin and characterization of cytochrome P450 and UDP-glucuronosyltransferase enzymes in human liver microsomes

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dc.contributor.authorW Y Song-
dc.contributor.authorH Y Ji-
dc.contributor.authorN I Baek-
dc.contributor.authorTae Sook Jeong-
dc.contributor.authorH S Lee-
dc.date.accessioned2017-04-19T09:21:24Z-
dc.date.available2017-04-19T09:21:24Z-
dc.date.issued2010-
dc.identifier.issn0253-6269-
dc.identifier.uri10.1007/s12272-010-1214-1ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/9973-
dc.description.abstractJaceosidin is an active component in Artemisia species as well as Eupatorium species and it exhibits antiallergic, anticancer, antioxidant, anti-inflammatory, and antimutagenic activities. Jaceosidin was metabolized to jaceosidin glucuronide, 6-O-desmethyljaceosidin, hydroxyjaceosidin, 6-O-desmethyljaceosidin glucuronide, and hydroxyjaceosidin glucuronide in human liver microsomes. This study characterized the human liver cytochrome P450 (CYP) and UDPglucuronosyltransferase (UGT) enzymes responsible for the metabolism of jaceosidin. CYP1A2 was identified as the major enzyme responsible for the formation of 6-O-desmethyljaceosidin and hydroxyjaceosidin from jaceosidin on the basis of a combination of correlation analysis and experiments including immuno-inhibition, chemical inhibition in human liver microsomes, and metabolism by human cDNA-expressed CYP enzymes. Jaceosidin glucuronidation was catalyzed by UGT1A1, UGT1A3, UGT1A7, UGT1A8, UGT1A9, and UGT1A10. These results suggest that the pharmacokinetics of jaceosidin may be dramatically affected by polymorphic CYP1A2, UGT1A1, and UGT1A7 responsible for the metabolism of jaceosidin or by the coadministration of relevant CYP1A2 or UGT inhibitors or inducers.-
dc.publisherPharmaceutical Soc Korea-
dc.titleIn vitro metabolism of Jaceosidin and characterization of cytochrome P450 and UDP-glucuronosyltransferase enzymes in human liver microsomes-
dc.title.alternativeIn vitro metabolism of Jaceosidin and characterization of cytochrome P450 and UDP-glucuronosyltransferase enzymes in human liver microsomes-
dc.typeArticle-
dc.citation.titleArchives of Pharmacal Research-
dc.citation.number12-
dc.citation.endPage1996-
dc.citation.startPage1985-
dc.citation.volume33-
dc.contributor.affiliatedAuthorTae Sook Jeong-
dc.contributor.alternativeName송원영-
dc.contributor.alternativeName지혜영-
dc.contributor.alternativeName백남인-
dc.contributor.alternativeName정태숙-
dc.contributor.alternativeName이혜숙-
dc.identifier.bibliographicCitationArchives of Pharmacal Research, vol. 33, no. 12, pp. 1985-1996-
dc.identifier.doi10.1007/s12272-010-1214-1-
dc.subject.keywordCYP1A2-
dc.subject.keywordGlucuronidation-
dc.subject.keywordHydroxylation-
dc.subject.keywordJaceosidin metabolism-
dc.subject.keywordO-Demethylation-
dc.subject.keywordUGTs-
dc.subject.localCYP1A2-
dc.subject.localGlucuronidation-
dc.subject.localglucuronidation-
dc.subject.localHydroxylation-
dc.subject.localhydroxylation-
dc.subject.localJaceosidin metabolism-
dc.subject.localO-Demethylation-
dc.subject.localUGT-
dc.subject.localUGTs-
dc.description.journalClassY-
Appears in Collections:
Division of Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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