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Cultured mouse embryos metabolize benzo(a)pyrene during early gestation: genetic differences detectable by sister chromatid exchange

Journal Article · · Proc. Natl. Acad. Sci. U.S.A.; (United States)

Mouse embryos explanted at 7 1/2 or 8 1/2 days of gestation were cultured in medium containing benzo(a)pyrene and supplemented with 5-bromodeoxyuridine to allow detection of sister chromatid exchanges. The murine Ah locus regulates the inducible metabolism of polycyclic hydrocarbons such as benzo(a)pyrene. A high frequency of sister chromatid exchanged was induced by benzo(a)pyrene in embryos from three Ah- responsive inbred strains; there was little or no increase in two Ah-nonresponsive inbred strains. Benzo(a)pyrene also induced sister chromatid exchanges in the Ah-responsive recombinant inbred line B6NXAKN-12 but not in the Ah-nonresponsive recombinant inbred line B6NXAKN-3. Sister chromatid exchange in cultured Ah-responsive mouse embryos was thus shown to be a sensitive assay. These data provide direct evidence that genetically responsive mouse embryos possess the subcellular processes necessary for induction of enzymes that metabolize benzo(a)pyrene to its chemically active form(s). Both the Ah regulatory gene product and the structural gene product therefore appear to be functional at an early embryonic age. Furthermore, this metabolic capacity may play an important role in the damage to embryonic cells by polycyclic hydrocarbons.

OSTI ID:
5098085
Journal Information:
Proc. Natl. Acad. Sci. U.S.A.; (United States), Journal Name: Proc. Natl. Acad. Sci. U.S.A.; (United States) Vol. 77:6; ISSN PNASA
Country of Publication:
United States
Language:
English