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dc.contributor.authorKim, S-
dc.contributor.authorKim, T-
dc.contributor.authorAhn, K-
dc.contributor.authorPark, WK-
dc.contributor.authorNah, SY-
dc.contributor.authorRhim, H-
dc.date.accessioned2024-01-21T06:10:27Z-
dc.date.available2024-01-21T06:10:27Z-
dc.date.created2021-09-05-
dc.date.issued2004-10-15-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137133-
dc.description.abstractWe previously reported that ginseng, a well-known herbal medicine, inhibited NMDA receptors in cultured hippocampal neurons. Here, we further examined the detailed mechanism of ginseng-mediated inhibition using its main active ingredient, ginsenoside Rg(3). Co-application of ginsenoside Rg(3) with increasing concentrations of NMDA did not change the EC50 of NMDA to the receptor, suggesting that ginsenoside Rg(3) inhibits NMDA receptors without competing with the NMDA-binding site. Ginsenoside Rg(3)-mediated inhibition also occurred in a distinctive manner from the well-characterized NMDA receptor open channel blocker, MK-801. However, ginsenoside Rg(3) produced its effect in a glycine concentration-dependent manner and shifted the glycine concentration-response curve to the right without changing the maximal response, suggesting the role of ginsenoside Rg(3) as a competitive NMDA receptor antagonist. We also demonstrated that ginsenoside Rg(3) significantly protected neurons against NMDA insults. Therefore, these results suggest that ginsenoside Rg(3) protects NMDA-induced neuronal death via a competitive interaction with the glycine-binding site of NMDA receptors in cultured hippocampal neurons. (C) 2004 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectCHANNEL CURRENTS-
dc.subjectPANAX-GINSENG-
dc.subjectGLUTAMATE-
dc.subjectACID-
dc.subjectNEUROTOXICITY-
dc.subjectINGREDIENT-
dc.subjectBINDING-
dc.subjectMK-801-
dc.subjectBRAIN-
dc.subjectRB-1-
dc.titleGinsenoside Rg(3) antagonizes NMDA receptors through a glycine modulatory site in rat cultured hippocampal neurons-
dc.typeArticle-
dc.identifier.doi10.1016/j.bbrc.2004.08.106-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.323, no.2, pp.416 - 424-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume323-
dc.citation.number2-
dc.citation.startPage416-
dc.citation.endPage424-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000224076900009-
dc.identifier.scopusid2-s2.0-4544338752-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusCHANNEL CURRENTS-
dc.subject.keywordPlusPANAX-GINSENG-
dc.subject.keywordPlusGLUTAMATE-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusNEUROTOXICITY-
dc.subject.keywordPlusINGREDIENT-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusMK-801-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusRB-1-
dc.subject.keywordAuthorginseng-
dc.subject.keywordAuthorginsenoside Rg(3)-
dc.subject.keywordAuthorneurotoxicity-
dc.subject.keywordAuthorNMDA-
dc.subject.keywordAuthorMTT assay-
dc.subject.keywordAuthorglycine-
dc.subject.keywordAuthorintracellular Ca2+-
dc.subject.keywordAuthorfura-2/AM-
dc.subject.keywordAuthorhippocampal neurons-
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