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

Cited 24 time in Web of Science Cited 23 time in Scopus
Authors
Kim, Hyun-Jung; Yoon, Hye-Ran; Washington, Stacy; Chang, In I; Oh, Young J; Surh, Young-Joon
Issue Date
1997-12
Citation
Neuroscience Letters, Vol.238 No.3, pp.95-98
Keywords
salsolinoltetrahydroisoquinoline alkaloidredox cyclingDNA strand scissionPC12 cellscytotoxicitytransition metal ion
Abstract
The 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.
ISSN
0304-3940
URI
https://hdl.handle.net/10371/172875
DOI
https://doi.org/10.1016/S0304-3940(97)00866-5
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Graduate School of Convergence Science and Technology (융합과학기술대학원)Dept. of Molecular and Biopharmaceutical Sciences (분자의학 및 바이오제약학과)Journal Papers (저널논문_분자의학 및 바이오제약학과)
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