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Garlic (Allium sativum) extract inhibits lipopolysaccharide-induced toll-like receptor 4 dimerization

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dc.contributor.authorYoun, Hyting-Sun-
dc.contributor.authorLim, Hyo Jin-
dc.contributor.authorLee, Hwa Jin-
dc.contributor.authorHwang, Daniel-
dc.contributor.author양미희-
dc.contributor.authorJeon, Raok-
dc.contributor.authorRyu, Jae-Ha-
dc.date.available2021-02-22T14:47:09Z-
dc.date.issued2008-02-
dc.identifier.issn0916-8451-
dc.identifier.issn1347-6947-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/14355-
dc.description.abstractGarlic has long been used as a folk medicine. Numerous studies have demonstrated that a garlic extract and its sulfur-containing compounds inhibited nuclear factor kappa B (NF-kappa B) activation induced by various receptor agonists including lipopolysaccharide (LPS). Toll-like receptors (TLRs) play a key role in sensing diverse microbial products and inducing innate immune responses. The dimerization of TLR4 is required for the activation of downstream signaling pathways, including NF-kappa B. Therefore, TLR4 dimerization may be one of the first lines of regulation in activating LPS-induced signaling pathways. We report here biochemical evidence that the ethyl acetate fraction of garlic inhibited the LPS-induced dimerization of TLR4, resulting in the inhibition of NF-kappa B activation and the expression of cyclooxygenase 2 and inducible nitric oxide synthase. Our results demonstrate for the first time that a garlic extract can directly inhibit the TLRs-mediated signaling pathway at the receptor level. These results shed a new insight into understanding how garlic modulates the immune responses that could modify the risk of many chronic diseases.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherTAYLOR & FRANCIS LTD-
dc.titleGarlic (Allium sativum) extract inhibits lipopolysaccharide-induced toll-like receptor 4 dimerization-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1271/bbb.70434-
dc.identifier.scopusid2-s2.0-40449120671-
dc.identifier.wosid000253892800013-
dc.identifier.bibliographicCitationBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, v.72, no.2, pp 368 - 375-
dc.citation.titleBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY-
dc.citation.volume72-
dc.citation.number2-
dc.citation.startPage368-
dc.citation.endPage375-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusDIALLYL SULFIDE-
dc.subject.keywordPlusCUTTING EDGE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCOMPONENT-
dc.subject.keywordPlusTLR4-
dc.subject.keywordPlusTOLL-LIKE-RECEPTOR-4-
dc.subject.keywordPlusHOMODIMERIZATION-
dc.subject.keywordAuthorgarlic-
dc.subject.keywordAuthortoll-like receptor-
dc.subject.keywordAuthorcyclooxygenase-
dc.subject.keywordAuthornitric oxide synthase-
dc.identifier.urlhttps://doi.org/10.1271/bbb.70434-
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