Altered ganglioside patterns accompany the anti-inflammatory activity of luteolin in lipopolysaccharide-stimulated Raw 264.7 = 리포폴리 사카아리드가 처리된 RAW264.7에서 루테올린에 의한 갱글리오시드의 발현변화와 항염증 반응

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dc.contributor.authorJ S Ryu-
dc.contributor.authorM U Lim-
dc.contributor.authorM R Hwang-
dc.contributor.authorH K Min-
dc.contributor.authorG Moussavou-
dc.contributor.authorJi Su Kim-
dc.contributor.authorSun-Uk Kim-
dc.contributor.authorK Ko-
dc.contributor.authorY H Cho-
dc.contributor.authorS Y Nam-
dc.contributor.authorKyu Tae Chang-
dc.contributor.authorY K Choo-
dc.date.accessioned2017-04-19T09:36:12Z-
dc.date.available2017-04-19T09:36:12Z-
dc.date.issued2012-
dc.identifier.issn1976-7447-
dc.identifier.uri10.12729/jbr.2012.13.4.287ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11135-
dc.description.abstractFlavonoids have a range of biological activities, including anti-allergic, anti-inflammatory, anti-microbial, and anti-cancer activities, as shown by in vitro studies. In this study, we investigated whether luteolin can be applied to the suppression of lipopolysaccharide (LPS)-stimulated inflammatory responses in murine macrophages. Luteolin was found to reduce nitric oxide (NO) production from LPS-stimulated Raw 264.7 cells. moreover, expression of inducible nitric oxide synthetase (iNOS), cyclooxygenase-2 (COX-2) and pro-inflammatory cytokine tumor necrotic factor-α (TNF-α) at the mRNA and protein levels were decreased. These inhibitory effects were found to be caused by the blockage of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) activation and the phosphorylation of mitogen-activated protein (MAP) kinase famaily, extracellular signal-regulated kinases 1/2 (ERK1/2), c-Jun N-terminal kinase (JNK) and p38 MAP kinase. Furthermore, pre-treatment with luteolin reduced ganglioside expression levels and inhibited GT1b expression in Raw 264.7 cells. On the basis of these observations, we suggest that luteolin has potential as an anti-inflammatory drug candidate, and ganglioside GT1b may play a role in the inflammatory.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleAltered ganglioside patterns accompany the anti-inflammatory activity of luteolin in lipopolysaccharide-stimulated Raw 264.7 = 리포폴리 사카아리드가 처리된 RAW264.7에서 루테올린에 의한 갱글리오시드의 발현변화와 항염증 반응-
dc.title.alternativeAltered ganglioside patterns accompany the anti-inflammatory activity of luteolin in lipopolysaccharide-stimulated Raw 264.7-
dc.typeArticle-
dc.citation.titleJournal of Biomedical Research-
dc.citation.number4-
dc.citation.endPage294-
dc.citation.startPage287-
dc.citation.volume13-
dc.contributor.affiliatedAuthorJi Su Kim-
dc.contributor.affiliatedAuthorSun-Uk Kim-
dc.contributor.affiliatedAuthorKyu Tae Chang-
dc.contributor.alternativeName류재성-
dc.contributor.alternativeName임맑음-
dc.contributor.alternativeName황미란-
dc.contributor.alternativeName민현기-
dc.contributor.alternativeNameMoussavou-
dc.contributor.alternativeName김지수-
dc.contributor.alternativeName김선욱-
dc.contributor.alternativeName고기성-
dc.contributor.alternativeName조영호-
dc.contributor.alternativeName남상윤-
dc.contributor.alternativeName장규태-
dc.contributor.alternativeName추영국-
dc.identifier.bibliographicCitationJournal of Biomedical Research, vol. 13, no. 4, pp. 287-294-
dc.identifier.doi10.12729/jbr.2012.13.4.287-
dc.subject.keywordluteolin-
dc.subject.keywordinflammation-
dc.subject.keywordlipopolysaccharide-
dc.subject.keywordgangliosides-
dc.subject.keywordRaw 264.7 macrophage-
dc.subject.localluteolin-
dc.subject.localLuteolin-
dc.subject.localInflammation-
dc.subject.localinflammation-
dc.subject.localnflammation-
dc.subject.localLipopolysaccharide-
dc.subject.localLipopolysaccharide (LPS)-
dc.subject.localLipopolysaccharides-
dc.subject.locallipopolysaccharide-
dc.subject.locallipopolysaccharide (LPS)-
dc.subject.localgangliosides-
dc.subject.localRAW 264.7 macrophage-
dc.subject.localRAW 264.7 macrophages-
dc.subject.localRaw 264.7 macrophage-
dc.description.journalClassN-
Appears in Collections:
Jeonbuk Branch Institute > Primate Resources Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
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