Binding of nitrobenzene to hepatic DNA and hemoglobin at low doses in mice

Nitrobenzene (NB) is a widely used industrial chemical, and is considered a hazardous air pollutant. Evidence has recently showed that nitrobenzene is an animal carcinogen. We investigated the binding of 14C-NB to hepatic DNA and Hb in mice at low doses using an ultrasensitive method of accelerator mass spectrometry (AMS). In a dose-response profile, NB-DNA and NB-Hb adduct levels increased with increasing administered doses from 0.1 microg/kg b.w. to 10 mg/kg b.w. with a good linearity in a log/log presentation. At 2 h after NB administration, NB-DNA adduct levels were about twofold greater than that of NB-Hb at all doses. In the time course study NB-DNA adduct levels reduced rapidly through an exponential decay profile, whereas NB-Hb adducts showed a different decay mode, declining rather slowly to low levels. Our findings on the genotoxicity of NB do furnish a significant evidence in support of the probable carcinogenic property of NB previously reported.