Abstract
The effect of caffeine on the genotoxicity of several carcinogenic compounds representing various classes of chemicals was investigated in a panel of V79 Chinese hamster cells genetically engineered to express cytochromes P4501A1 and P4501A2 and differing in their expression of N-acetyltransferases. The formation of micronuclei served as genetic endpoint. The results show that caffeine increases the number of micronuclei induced by 2-aminoanthracene several fold in the test cell lines. The lowest concentration of caffeine enhancing 2-aminoanthracene-induced genotoxicity was 100 nM. Caffeine also potentiated the genotoxicity of aflatoxin B 1, 2-amino-3-methylimidazo[4,5-f]-quinoline, N-methyl- N-nitro- N-nitrosoguanidine, 1,6-dinitropyrene, and 7,8-diol-benzo[a]pyrene. Overall, caffeine lowered the effective genotoxic concentrations of these agents by a factor of about three. In contrast, the genotoxic effect of 4-( N-methyl- N-nitrosamino)-1-(3-pyridyl)-1-butanone is markedly decreased in the presence of caffeine. The results indicate that caffeine may modulate the genotoxicity of chemical carcinogens by different mechanisms.
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