6533b839fe1ef96bd12a673e

RESEARCH PRODUCT

Binding of benzo(a)pyrene metabolites to cellular DNA in perfused rat lungs

B. Deckers-schmelzleG. F. KahlRegine KahlE. Klaus

subject

MalePharmacologyCytochromebiologyProteinsNucleosidesDNAGeneral MedicineIn Vitro TechniquesMonooxygenaseRatschemistry.chemical_compoundchemistryBiochemistryBenzo(a)pyreneSephadexbiology.proteinAnimalsRNAPyreneInducerBenzopyrenesLungNucleosideDNA

description

The influence of pretreatment with monooxygenase inducers on total irreversible binding of metabolically activated [3H]-benzo(a)pyrene to cellular DNA and the formation of benzo(a)pyrene metabolite-deoxyribonucleoside adducts after cytochrome P-448 induction was studied in perfused rat lungs. Pretreatment with the cytochrome P-448 inducer beta-naphthoflavone increasing binding by a factor of 23. In lungs of induced animals, 0.45 pmoles of benzo(a)pyrene equivalents were bound per mg DNA. Binding to RNA and to protein was also considerably induced by beta-naphthoflavone. Phenobarbital treatment did not significantly increase binding to cellular macromolecules of rat lung. Analysis of hydrolyzed DNA of lungs from beta-naphthoflavone-treated rats by Sephadex LH 20 chromatography revealed the formation of at least two nucleoside adducts with metabolically activated benzo(a)pyrene one of which is probably due to modification of the DNA with a benzo(a)pyrene-7, 8-dihydrodiol-9, 10-epoxide and the other to modification of DNA with secondary metabolites of benzo(a)pyrene phenols.

yearjournalcountryeditionlanguage
1978-07-01Naunyn-Schmiedeberg's Archives of Pharmacology
https://doi.org/10.1007/bf00498059