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Necrosis inhibitor-5 (NecroX-5), attenuates MPTP-induced motor deficits in a zebrafish model of Parkinson's disease

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dc.contributor.authorLiu, Jun-Cheng-
dc.contributor.authorKoppula, Sushruta-
dc.contributor.authorHuh, Se-Jong-
dc.contributor.authorPark, Pyo-Jam-
dc.contributor.authorKim, Chul-Geun-
dc.contributor.authorLee, Chang-Joong-
dc.contributor.authorKim, Chan-Gil-
dc.date.accessioned2022-07-07T04:26:56Z-
dc.date.available2022-07-07T04:26:56Z-
dc.date.issued2015-12-
dc.identifier.issn1976-9571-
dc.identifier.issn2092-9293-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/143047-
dc.description.abstractIn the present study, necrosis inhibitor-5 (NecroX-5), a novel Cyclopentylamino carboxymethylthiazolylindole (NecroX) series compound was investigated for its protective role against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity in a zebrafish model of Parkinson's disease (PD). MPTP-induced locomotor behavior was measured in zebrafish larvae and the protein expression level of tyrosine hydroxylase (TH) was estimated in zebrafish larva homogenates. MPTP (15 mu M) induced a significant (p < 0.05) impairment in zebrafish larvae locomotor behavior. Treatment with NecroX-5 at various doses (3.75, 7.5 and 15 mu M) significantly and dose dependently (p < 0.05) restored MPTP-induced locomotor impairments in zebrafish larvae. Further, NecroX-5 significantly attenuated the MPTP-induced decrease in zebrafish TH protein expression levels. The effects observed by NecroX-5 were almost two fold higher when compared with the antioxidant, minocycline. In conclusion, the neuroprotective activity exhibited by NecroX-5 by attenuating MPTP-induced locomotor impairments and dopaminergic TH expression in zebrafish warrants further development of NecroX-5 as a novel neuroprotectant in the treatment of neurodegenerative disorders including PD.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisher한국유전학회-
dc.titleNecrosis inhibitor-5 (NecroX-5), attenuates MPTP-induced motor deficits in a zebrafish model of Parkinson's disease-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s13258-015-0364-4-
dc.identifier.scopusid2-s2.0-84948585093-
dc.identifier.wosid000365756700012-
dc.identifier.bibliographicCitationGenes & Genomics, v.37, no.12, pp 1073 - 1079-
dc.citation.titleGenes & Genomics-
dc.citation.volume37-
dc.citation.number12-
dc.citation.startPage1073-
dc.citation.endPage1079-
dc.type.docTypeArticle-
dc.identifier.kciidART002057876-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusNEURODEGENERATIVE DISEASES-
dc.subject.keywordPlusDOPAMINERGIC-NEURONS-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlus1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE-
dc.subject.keywordPlusNEUROPROTECTION-
dc.subject.keywordPlusNEUROTOXICITY-
dc.subject.keywordPlusDIENCEPHALON-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusTARGETS-
dc.subject.keywordAuthorNecroX-
dc.subject.keywordAuthorOxidative stress-
dc.subject.keywordAuthorTyrosine hydroxylase-
dc.subject.keywordAuthorZebrafish-
dc.subject.keywordAuthorParkinson's disease-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s13258-015-0364-4-
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