Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Metabolism and DNA binding of BaP in the presence of complex organic mixtures

Conference ·
OSTI ID:5003325
Previous studies have shown that the mutagenic, carcinogenic and DNA binding activities of benzo(a)pyrene (BaP) were decreased when BaP was coadministered with complex organic mixtures. We have continued these studies to identify the components of the mixture that were responsible for this effect. For this study a high-boiling coal liquid was separated into aliphatic, polycyclic aromatic hydrocarbon (PAH), nitrogen-containing polycyclic aromatic compounds (NPAC) and oxygen containing PAH fractions (HPAH); these were spiked with /sup 3/H-BaP, administered dermally to mice and DNA isolated twenty-four hours later. Binding of BaP, as estimated by radioactivity associated the DNA, decreased to 47, 55 and 66% of that for the same dose of BaP alone for the PAH, NPAC and HPAH fractions, respectively. In vitro studies with Aroclor-induced rat liver S9 demonstrated that the rate of metabolism of BaP decreased when it was coadministered with the mixtures but that the BaP metabolite profiles were similar for BaP alone and in the presence of the mixture. These data suggest that the differences in mutagenic, and presumable carcinogenic activities, for BaP, when administered with the complex mixture, were due to decreased rates of conversion of BaP to reactive metabolites. 15 refs., 2 figs., 3 tabs.
Research Organization:
Pacific Northwest Lab., Richland, WA (USA)
DOE Contract Number:
AC06-76RL01830
OSTI ID:
5003325
Report Number(s):
PNL-SA-13221; CONF-861044-1; ON: DE87001656
Country of Publication:
United States
Language:
English