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Preparative isolation of sargachromanol E from Sargassum siliquastrum by centrifugal partition chromatography and its anti-inflammatory activity

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dc.contributor.authorLee, Ji-Hyeok-
dc.contributor.authorKo, Ju-Young-
dc.contributor.authorSamarakoon, Kalpa-
dc.contributor.authorOh, Jae-Young-
dc.contributor.authorHeo, Soo-Jin-
dc.contributor.authorKim, Chul-Young-
dc.contributor.authorNah, Jae-Woon-
dc.contributor.authorJang, Mi-Kyeong-
dc.contributor.authorLee, Jung-Suck-
dc.contributor.authorJeon, You-Jin-
dc.date.accessioned2021-06-23T02:03:29Z-
dc.date.available2021-06-23T02:03:29Z-
dc.date.created2021-01-21-
dc.date.issued2013-12-
dc.identifier.issn0278-6915-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/26289-
dc.description.abstractCentrifugal partition chromatography (CPC) can be used to isolate various bioactive compounds from natural materials by one-step. We confirmed antioxidative compounds existed in chloroform (CHCl3) fraction of Sargassum siliquastrum using online-HPLC. Fractions (A, B, C, D and E) were separated from the CHCl3 fraction by preparative CPC (n-hexane:ethyl acetate:methanol:water, 5:5:7:3, v/v). In this study, we proved that the isolated compounds exhibit anti-inflammatory activities using lipopolysaccharide (LPS) stimulated RAW 264.7 macrophages. The fraction A which exhibited the strongest inhibitory effect on nitric oxide (NO) production level, was confirmed as sargachromanol E by LC-MS-ESI, H-1 NMR and C-13 NMR data. The sargachromanol E significantly reduced the inflammatory response in LPS induced macrophages, decreasing LPS-induced transcription factor of pro-inflammatory cyclooxygenase-2, NO synthase, phosphate P38, phosphate ERK1/2, LPS-stimulated tumor-necrosis factor alpha, interleukin-1 beta and prostaglandin E2 release. In conclusion, it was suggested that sargachromanol E inhibited inflammation in LPS induced RAW 264.7 cells via MAPK pathway. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titlePreparative isolation of sargachromanol E from Sargassum siliquastrum by centrifugal partition chromatography and its anti-inflammatory activity-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chul-Young-
dc.identifier.doi10.1016/j.fct.2013.08.010-
dc.identifier.scopusid2-s2.0-84883680989-
dc.identifier.wosid000329960400009-
dc.identifier.bibliographicCitationFOOD AND CHEMICAL TOXICOLOGY, v.62, pp.54 - 60-
dc.relation.isPartOfFOOD AND CHEMICAL TOXICOLOGY-
dc.citation.titleFOOD AND CHEMICAL TOXICOLOGY-
dc.citation.volume62-
dc.citation.startPage54-
dc.citation.endPage60-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusBROWN-ALGA-
dc.subject.keywordPlusPLASTOQUINONES-
dc.subject.keywordPlusPURIFICATION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSEPARATION-
dc.subject.keywordPlusEXTRACT-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordAuthorCentrifugal partition chromatography-
dc.subject.keywordAuthorSargachromanol E-
dc.subject.keywordAuthorSargassum siliquastrum-
dc.subject.keywordAuthorAntiinflammatory activity-
dc.subject.keywordAuthorMAPK pathway-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0278691513005528?via%3Dihub-
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