Published May 29, 1986 | Version v1
Journal article

Comparative studies of the mechanisms of paraquat and 1-methyl-4-phenylpyridine (MPP+) cytotoxicity

  • 1. Univ. of California, Berkeley

Description

1-Methyl-4-phenylpyridine (MPP+) is the putative toxic metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and is structurally similar to the herbicide paraquat (PQ++). The authors have therefore compared the effects of MPP+ and PQ++ on isolated rat hepatocytes. PQ++ generates reactive oxygen species within cells by redox cycling and its toxicity to hepatocytes was potentiated by pretreatment with 1,3-bis(2-chlorethyl)-1-nitrosourea (BCNU), an inhibitor of glutathione reductase. In BCNU-treated cells, PQ++ caused GSH depletion, lipid peroxidation and cell death. These cytotoxic effects were prevented by the antioxidant N,N'-diphenyl-p-phenylenediamine (DPPD) and the iron-chelating agent desferrioxamine. MPP+ also caused GSH depletion in BCNU-treated hepatocytes but its cytotoxicity was not markedly affected by BCNU, nor was it accompanied by significant lipid peroxidation. DPPD and desferrioxamine also failed to prevent MPP+-induced cell death

Additional details

Publishing Information

Journal Title
Biochem. Biophys. Res. Commun.
Journal Volume
137
Journal Issue
1
Series
Biochem. Biophys. Res. Commun.
Journal Page Range
303-309
ISSN
0006-291X
CODEN
BBRCA