Differential Cytotoxicities of N-Methyl-β-Carbolinium Analogues of MPP+ in PC12 Cells: Insights into Potential Neurotoxicants in Parkinson's Disease
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1471-4159.1994.62041503.x/fullpdf
Reference48 articles.
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2. Structure-neurotoxicity trends in analogues of l-methyl-4-phenylpyridinium (MPP+), the cytotoxic metabolite of the dopaminergic neurotoxin MPTP;Arora;Life Sci.,1990
3. l-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine- and 1-methyl-4-(2′-ethylphenyl)-1,2,3,6-tetrahydropyridine- induced toxicity in PC12 cells: role of monoamine oxidase A;Basma;J. Neurochem.,1990
4. 1-Methyl-4-(2′-ethylphenyl)- 1,2,3,6-tetrahydropyridine-induced toxicity in PC12 cells is enhanced by preventing glycolysis;Basma;J. Neurochem.,1992
5. In vitro study of the aromatic hydroxylation of 1-methyltetrahydro-β- carboline (methtryptoline) in rat;Beck;Chem. Biol. Interact.,1988
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