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Iristectorigenin B isolated from Belamcanda chinensis is a liver X receptor modulator that increases ABCA1 and ABCG1 expression in macrophage RAW 264.7 cells

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dc.contributor.authorJun, Hee-jin-
dc.contributor.authorHoang, Minh-Hien-
dc.contributor.authorLee, Jin Woo-
dc.contributor.authorYaoyao, Jia-
dc.contributor.authorLee, Ji-Hae-
dc.contributor.authorLee, Dong-Ho-
dc.contributor.authorLee, Hak-Ju-
dc.contributor.authorSeo, Woo-Duck-
dc.contributor.authorHwang, Bang Yeon-
dc.contributor.authorLee, Sung-Joon-
dc.date.accessioned2021-09-06T12:55:11Z-
dc.date.available2021-09-06T12:55:11Z-
dc.date.created2021-06-14-
dc.date.issued2012-12-
dc.identifier.issn0141-5492-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/106899-
dc.description.abstractA novel liver X receptor (LXR) modulator, iristectorigenin B isolated from Belamcanda chinensis, stimulated the transcriptional activity of both LXR-alpha and LXR-beta. In macrophages, iristectorigenin B suppressed cholesterol accumulation in a dose-dependent manner and induced the transcriptional activation of LXR-alpha/-beta-responsive genes, ATP-binding cassette transporters A1 and G1. It did not induce hepatic lipid accumulation nor the expression of the lipogenesis genes sterol regulatory element-binding protein-1c, fatty acid synthase, and stearoyl-CoA desaturase-1. Iristectorigenin B thus is a dual-LXR agonist that regulates the expression of key genes in cholesterol homeostasis in macrophage cells without inducing hepatic lipid accumulation.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectLXR AGONISTS-
dc.subjectCHOLESTEROL-
dc.subjectLIPOGENESIS-
dc.subjectDISEASE-
dc.subjectMICE-
dc.titleIristectorigenin B isolated from Belamcanda chinensis is a liver X receptor modulator that increases ABCA1 and ABCG1 expression in macrophage RAW 264.7 cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Dong-Ho-
dc.identifier.doi10.1007/s10529-012-1036-y-
dc.identifier.scopusid2-s2.0-84868448474-
dc.identifier.wosid000310587500009-
dc.identifier.bibliographicCitationBIOTECHNOLOGY LETTERS, v.34, no.12, pp.2213 - 2221-
dc.relation.isPartOfBIOTECHNOLOGY LETTERS-
dc.citation.titleBIOTECHNOLOGY LETTERS-
dc.citation.volume34-
dc.citation.number12-
dc.citation.startPage2213-
dc.citation.endPage2221-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusLXR AGONISTS-
dc.subject.keywordPlusCHOLESTEROL-
dc.subject.keywordPlusLIPOGENESIS-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusMICE-
dc.subject.keywordAuthorBelamcanda chinensis-
dc.subject.keywordAuthorCholesterol-
dc.subject.keywordAuthorIristectorigenin B-
dc.subject.keywordAuthorLXR modulator-
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