| Abstrakt: |
Indeno[l, 2, 3-cd]pyrene is a ubiquitous environmental pollutant which is active as a tumor initiator and complete carcinogen on mouse skin and is carcinogenic in rat lung. The major metabolites of indeno[l, 2, 3-cd]pyrene as formed in vivo in mouse skin have been identified. 8-Hydroxyindeno[1, 2, 3-cd]pyrene is the most abundant metabolite identified. 9-Hydroxyindeno[l, 2, 3-cd]pyrene and -l, 2-dihydro-l, 2-dihydroxyindeno[l, 2, 3-cd]pyrene are also major metabolites in mouse skin. Several minor metabolites were also identified. Among these are -l, 2-dihydro-l, 2, 3-tri-hydroxyindeno[l, 2, 3-cd]pyrene, *ra/w-l>2-dihydro-l, 2, 9-tri-hydroxyindeno[l, 2, 3-cd]pyrene, indeno[l, 2, 3-cd]pyreiie-l, 2-dione, and 10-hydroxyindeno[l, 2, 3-cd]pyrene. The tumor-initiating activity of several of the major metabolites of indeno[l,2,3-cd]pyrene has been investigated on mouse skin. -l,2-dihyddro-1,2-d1hydn)xymdeno[l,2,3-cd]pyrene and l,2-dihydro-l,2-epoxyindeno[l,2,3-cd]pyrene both produced an 80% incidence of tumor-bearing mice at a total initiating dose of 1.0 mg. The activity of this K-region dihydrodiol and K-region oxide was, however, less than that of the parent hydrocarbon. These data suggest that l,2-dihydro-l,2-epoxyindeno[l,2,3-cd]pyrene, which is an ultimate mutagenic metabolite of indeno[l,2,3-cd]pyrene, is not the ultimate tumorigenic metabolite on mouse skin. 8-Hydroxyindeno[l,2,3-cd]pyrene, which is mutagenic when assayed in the presence of a mkrosomal activation system, exhibited only weak tumor-initiating activity. These results indicate that the principal metabolic activation pathways associated with the mutagenic activity of indeno[l,2,3-cd]-pyrene are not related to its tumor-initiating activity on mouse skin. [ABSTRACT FROM PUBLISHER] |
