1-Methyl-2-nitrosoimidazole: Cytotoxic and glutathione depleting capabilities

We tested 1-methyl-2-nitrosoimidazole (IN% the two electron reduction product of 1-methyl-2-nitroimidazole (INO 2) for its in vitro cytotoxicity and glutathione (GSH) depleting capabilities. The half life of INO was shown to be dependent on cell concentration above 10 5 cells/ml, decreasing with inc...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 1989-04, Vol.16 (4), p.1015-1019
Hauptverfasser: Noss, Mark B., Panicucci, Rick, Mcclelland, Robert A., Rauth, Andrew M.
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Sprache:eng
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Zusammenfassung:We tested 1-methyl-2-nitrosoimidazole (IN% the two electron reduction product of 1-methyl-2-nitroimidazole (INO 2) for its in vitro cytotoxicity and glutathione (GSH) depleting capabilities. The half life of INO was shown to be dependent on cell concentration above 10 5 cells/ml, decreasing with increasing cell concentration up to 2 × 10 6 cells/ml. For a 10-fold decrease in cell concentration, from 10 6 to 10 5 cells/ml, the toxicity curve shifted 10-fold towards lower concentrations. At 10 6 cells/ml, INO depleted GSH, in the range of concentrations where toxicity was observed, down to a plateau of 15% of the control level at a concentration of 100 μM INO. Oxidized glutathione (GSSG) levels were not elevated significantly above control cultures at this concentration. INO 2, 1000 μM, did not deplete GSH under similar exposure conditions while 2-hydroxylamino-l-methylimidazole (INHOH) depleted GSH minimally at this same concentration. The nitroso intermediate may play a central role in the toxicity and GSH depleting capabilities of 2-nitroimidazoles in mammalian cells.
ISSN:0360-3016
1879-355X
DOI:10.1016/0360-3016(89)90906-1