Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9038338 | Toxicology in Vitro | 2005 | 7 Pages |
Abstract
T-514 (Peroxisomicine A1) from Karwinskia humboldtiana is a dimeric hydroxyanthracenone with a highly selective cytotoxic effect on tumor cells. We evaluated the metabolism of this compound in two in vitro systems (liver microsomes and hepatocytes) and assessed the cytotoxicity of its metabolites on normal and tumor cells. Microsomes (12.5, 125 and 250 μg of protein/ml) and hepatocytes (1 Ã 106 cells/ml) were incubated with the toxin (25 μM) for 0.5, 1, 3, 6, 9, 12 and 24 h and the samples were examined using chromatographic analysis and UV spectra. Two metabolites (M1 and M2) were detected in the rat microsomes and one (M1) in the monkey microsomes. The retention times and UV spectra of the peaks were very similar to those of the toxin T-514. M1 was isolated and identified as a mixture of two isomers. The cytotoxicity of the metabolites was evaluated in Chang liver and Hep G2 cells but they did not show the selective cytotoxic effect on tumor cells seen in the original compound.
Keywords
NOEHMBCUltraviolet–visible spectrumKarwinskia humboldtianaHMQCTLCnuclear magnetic resonanceHepatocytesMTTUV–Visnuclear overhauser effectNMRRetention timemass spectrumMetabolismLiver microsomesheteronuclear multiple bond correlationHeteronuclear Multiple Quantum Correlationhigh-performance liquid chromatographyHPLCthin-layer chromatography
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Authors
M. Gómez-Silva, L. Garza-Ocañas, N. Waksman, V. Rivas, A. Piñeyro-López,