TISSUE DISTRIBUTION AND MACROMOLECULAR BINDING OF EXTREMELY LOW-DOSESOF [C-14]-BENZENE IN B6C3F1 MICE

The tissue distribution and macromolecular binding of benzene was stud ied over a dose range spanning nine-orders of magnitude to determine t he nature of the dose-response and to establish benzene's internal dos imetry at doses encompassing human environmental exposures, [C-14]-Ben zene was administered to B6C3F1 male mice at doses ranging between 700 pg/kg and 500 mg/kg body wt. Tissues, DNA and protein were analyzed f or [C-14]-benzene content between 0 and 48 h post-exposure (625 Ng/kg and 5 mu g/kg dose) by accelerator mass spectrometry (AMS). [C-14]-Ben zene levels were highest in the liver and peaked within 0.5 h of expos ure, Liver DNA adduct levels peaked at 0.5 h, in contrast to bone marr ow DNA adduct levels, which peaked at 12-24 h, Dose-response assessmen ts at 1 h showed that adducts and tissue available doses increased lin early with administered dose up to doses of 16 mg/kg body wt. Tissue a vailable doses and liver protein adducts plateau above the 16 mg/kg do se, Furthermore, a larger percentage of the available dose in bone mar row bound to DNA relative to liver, Protein adduct levels were 9- to 4 3-fold greater than DNA adduct levels. These data show that benzene is bioavailable at human-relevant doses and that DNA and protein adduct formation is linear with dose over a dose range spanning eight orders of magnitude, Finally, these data show that the dose of bioactive meta bolites is greater to the bone marrow than the liver and suggests that protein adducts may contribute to benzene's hematoxicity.