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Inhibition of cytokine-induced vascular cell adhesion molecule-1 expression: possible mechanism for anti-atherogenic effect of Agastache rugosa : Inhibition of cytokine-induced vascular cell adhesion molecule-1 expression; possible mechanism for anti-atherogenic effect of Agastache rugosa

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dc.contributor.authorHong, JJ-
dc.contributor.authorChoi, JH-
dc.contributor.authorOh, SR-
dc.contributor.authorLee, HK-
dc.contributor.authorPark, JH-
dc.contributor.authorLee, KY-
dc.contributor.authorKim, JJ-
dc.contributor.authorJeong, TS-
dc.contributor.authorOh, GT-
dc.date.accessioned2023-07-07T08:05:06Z-
dc.date.available2023-07-07T08:05:06Z-
dc.date.created2022-05-13-
dc.date.issued2001-04-
dc.identifier.citationFEBS Letters, Vol.495 No.3, pp.142-147-
dc.identifier.issn0014-5793-
dc.identifier.urihttps://hdl.handle.net/10371/194899-
dc.description.abstractAdhesion molecules such as vascular cell adhesion molecule-1 (VCAM-1) play an important role during the early stages of atherogenesis. Agastache rugosa has an anti-atherogenic effect in low density lipoprotein receptor -/- mice. Moreover. A. rugosa reduced macrophage infiltration and VCAM-1 expression has been localized in aortic endothelium that overlies early foam cell lesions. This study ascertained that titianin (100 muM), a major component of A. rugosa inhibits the tumor necrotic factor-alpha (TNF-alpha)-induced expression of VCAM-1 by 74% in cultured human umbilical vein endothelial cells (HUVECs). Also, tilianin (100 muM) reduced TNF-alpha -induced activation of nuclear factor-kappaB in HUVECs. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleInhibition of cytokine-induced vascular cell adhesion molecule-1 expression: possible mechanism for anti-atherogenic effect of Agastache rugosa-
dc.title.alternativeInhibition of cytokine-induced vascular cell adhesion molecule-1 expression; possible mechanism for anti-atherogenic effect of Agastache rugosa-
dc.typeArticle-
dc.identifier.doi10.1016/S0014-5793(01)02379-1-
dc.citation.journaltitleFEBS Letters-
dc.identifier.wosid000168521700002-
dc.identifier.scopusid2-s2.0-0035957698-
dc.citation.endpage147-
dc.citation.number3-
dc.citation.startpage142-
dc.citation.volume495-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, JH-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusRECEPTOR-DEFICIENT MICE-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusATHEROSCLEROTIC LESIONS-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusRABBIT-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordAuthoratherosclerosis-
dc.subject.keywordAuthortilianin-
dc.subject.keywordAuthorvascular cell adhesion molecule-1-
dc.subject.keywordAuthormacrophage-
dc.subject.keywordAuthornuclear factor-kappa B-
dc.subject.keywordAuthorAgastache rugosa-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Laboratory Animal Medicine, Toxicologic Pathology

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