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Protective effect of casuarinin against glutamate-induced apoptosis in HT22 cells through inhibition of oxidative stress-mediated MAPK phosphorylation

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dc.contributor.authorSong, Ji Hoon-
dc.contributor.authorKang, Ki Sung-
dc.contributor.authorChoi, You-Kyung-
dc.date.available2020-02-27T16:41:21Z-
dc.date.created2020-02-06-
dc.date.issued2017-12-01-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/5374-
dc.description.abstractGlutamate is the major excitatory neurotransmitter in the central nervous system and is involved in oxidative stress during neurodegeneration. In the present study, casuarinin prevented glutamate-induced HT22 murine hippocampal neuronal cell death by inhibiting intracellular reactive oxygen species (ROS) production. Moreover, casuarinin reduced chromatin condensation and annexin-V-positive cell production induced by glutamate. We also confirmed the underlying protective mechanism of casuarinin against glutamate-induced neurotoxicity. Glutamate markedly increased the phosphorylation of extracellular signal regulated kinase (ERK)-1/2 and p38, which are crucial in oxidative stress-mediated neuronal cell death. Conversely, treatment with casuarinin diminished the phosphorylation of ERK1/2 and P38. In conclusion, the results of this study suggest that casuarinin, obtained from natural products, acts as potent neuroprotective agent by suppressing glutamate-mediated apoptosis through the inhibition of ROS production and activation of the mitogen activated protein kinase (MAPK) pathway. Thus, casuarinin can be a potential therapeutic agent in the treatment of neurodegenerative diseases. (C) 2017 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.subjectNEURONAL CELLS-
dc.subjectKINASE PATHWAYS-
dc.subjectCYCLE ARREST-
dc.subjectDEATH-
dc.subjectTOXICITY-
dc.subjectACTIVATION-
dc.subjectCULTURES-
dc.subjectERK1/2-
dc.subjectLINE-
dc.subjectBARK-
dc.titleProtective effect of casuarinin against glutamate-induced apoptosis in HT22 cells through inhibition of oxidative stress-mediated MAPK phosphorylation-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000415643400004-
dc.identifier.doi10.1016/j.bmcl.2017.10.075-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.27, no.23, pp.5109 - 5113-
dc.identifier.scopusid2-s2.0-85033216241-
dc.citation.endPage5113-
dc.citation.startPage5109-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume27-
dc.citation.number23-
dc.contributor.affiliatedAuthorKang, Ki Sung-
dc.contributor.affiliatedAuthorChoi, You-Kyung-
dc.type.docTypeArticle-
dc.subject.keywordAuthorCasuarinin-
dc.subject.keywordAuthorGlutamate-
dc.subject.keywordAuthorReactive oxygen species-
dc.subject.keywordAuthorMitogen-activated protein kinase-
dc.subject.keywordAuthorApoptosis-
dc.subject.keywordAuthorHT22 cells-
dc.subject.keywordPlusNEURONAL CELLS-
dc.subject.keywordPlusKINASE PATHWAYS-
dc.subject.keywordPlusCYCLE ARREST-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusTOXICITY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCULTURES-
dc.subject.keywordPlusERK1/2-
dc.subject.keywordPlusLINE-
dc.subject.keywordPlusBARK-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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