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DNA strand scission and PC12 cell death induced by salsolinol and copper

DC Field Value Language
dc.contributor.authorKim, Hyun-Jung-
dc.contributor.authorYoon, Hye-Ran-
dc.contributor.authorWashington, Stacy-
dc.contributor.authorChang, In I-
dc.contributor.authorOh, Young J-
dc.contributor.authorSurh, Young-Joon-
dc.date.accessioned2021-01-31T10:22:33Z-
dc.date.available2021-01-31T10:22:33Z-
dc.date.created2017-11-15-
dc.date.issued1997-12-
dc.identifier.citationNeuroscience Letters, Vol.238 No.3, pp.95-98-
dc.identifier.issn0304-3940-
dc.identifier.other5360-
dc.identifier.urihttps://hdl.handle.net/10371/172875-
dc.description.abstractThe naturally occurring neurotoxin, 1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (salsolinol; SAL), has been speculated to contribute to Parkinson's disease and neuropathology of chronic alcoholism. In the present study, we found the capability of SAL to cause DNA cleavage in the presence of Cu(II). Incubation of SAL and CuCl2 with calf thymus DNA caused strand breaks. Likewise, SAL in combination with Cu(II) mediated the strand scission in circle divide X174 RFI supercoiled DNA in a time-related manner. Neither Cu(II) nor the catechol alone induced any appreciable DNA cleavage. The reaction of SAL with Cu(II) was accompanied by the reduction of Cu(II) to Cu(I). Furthermore, SAL induced cell death in cultured PC12 cells, which was exacerbated by Cu(II). From these data, it seems likely that SAL undergoes redox cycling catalyzed by Cu(II) to generate reactive species which may be responsible for the neurotoxic action of this catechol isoquinoline. (C) 1997 Elsevier Science Ireland Ltd.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleDNA strand scission and PC12 cell death induced by salsolinol and copper-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.identifier.doi10.1016/S0304-3940(97)00866-5-
dc.citation.journaltitleNeuroscience Letters-
dc.identifier.wosid000071260100002-
dc.identifier.scopusid2-s2.0-0031555374-
dc.citation.endpage98-
dc.citation.number3-
dc.citation.startpage95-
dc.citation.volume238-
dc.identifier.sci000071260100002-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusNEUROTOXIN-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusCU(II)-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordAuthorsalsolinol-
dc.subject.keywordAuthortetrahydroisoquinoline alkaloid-
dc.subject.keywordAuthorredox cycling-
dc.subject.keywordAuthorDNA strand scission-
dc.subject.keywordAuthorPC12 cells-
dc.subject.keywordAuthorcytotoxicity-
dc.subject.keywordAuthortransition metal ion-
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  • College of Pharmacy
  • Department of Pharmacy
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