1. Possible role of salsolinol quinone methide in the decrease of RCSN-3 cell survival.
- Author
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Martinez-Alvarado P, Dagnino-Subiabre A, Paris I, Metodiewa D, Welch CJ, Olea-Azar C, Caviedes P, Caviedes R, and Segura-Aguilar J
- Subjects
- Animals, Biological Transport drug effects, Catalase genetics, Cell Line, Dicumarol pharmacology, Electron Spin Resonance Spectroscopy, Glutathione Peroxidase genetics, Neurons cytology, Neurons metabolism, RNA, Messenger genetics, Rats, Reverse Transcriptase Polymerase Chain Reaction, Substantia Nigra cytology, Superoxide Dismutase genetics, Transcription, Genetic drug effects, Cell Survival drug effects, Dopamine metabolism, Gene Expression Regulation, Enzymologic drug effects, Indolequinones, Indoles pharmacology, Isoquinolines pharmacology, Neurons drug effects, Quinones pharmacology
- Abstract
The endogenous dopamine-derived neurotoxin salsolinol was found to decrease survival in the dopaminergic neuronal cell line RCSN-3, derived from adult rat substantia nigra in a concentration-dependent manner (208 microM salsolinol induced a 50% survival decrease). Incubation of RCSN-3 cells with 100 micro;M dicoumarol and salsolinol significantly decreased cell survival by 2.5-fold (P < 0.001), contrasting with a negligible effect on RCHT cells, which exhibited nearly a 5-fold lower nomifensine-insensitive dopamine uptake. The levels of catalase and glutathione peroxidase mRNA were decreased when RCSN-3 cells were treated with 100 microM salsolinol alone or in the presence of 100 microM dicoumarol. In vitro oxidation of salsolinol to o-quinone catalyzed by lactoperoxidase gave the quinone methide and 1,2-dihydro-1-methyl-6,7-isoquinoline diol as final products of salsolinol oxidation as determined by NMR analysis. Evidence of the formation of salsolinol o-semiquinone radical has been provided by ESR studies during one-electron oxidation of salsolinol catalyzed by lactoperoxidase., (Copyright 2001 Academic Press.)
- Published
- 2001
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