ALPHA-NAPHTHOFLAVONE METABOLIZED BY 2,3,7,8-TETRACHLORODIBENZO(PARA)DIOXIN-INDUCED RAT-LIVER MICROSOMES - A POTENT CLASTOGEN IN CHINESE-HAMSTER OVARY CELLS
- 15 July 1987
- journal article
- research article
- Vol. 47 (14) , 3662-3666
Abstract
.alpha.-Naphthoflavone (ANF) is a widely used inhibitor of P-450-mediated metabolism. Previously, we have demonstrated that in vitro addidition of ANF to human lymphocytes produced significantly greater numbers of sister chromatid exchanges (SCEs) in samples from smokers compared to nonsmokers. In order to study the mechanism of this differential induction, we investigated the clastogenic activity of ANF as a consequence of metabolism by induced and uninduced rat liver microsomes. Exponentially growing Chinese hamster ovary cells were treated with ANF for 2 h in the presence or absence of microsomes, followed by incubation for 12 (chromosome aberrations) or 24 h (SCEs). ANF induced concentration (4 to 40 .mu.M)-dependent increases in SCEs and chromosome aberrations when coincubated with 2,3,7,8-tetrachlorodibenzo(p)dioxin-induced microsomes. At the lower concentrations of ANF, chromatid damage was most predominant, whereas at the higher concentrations, a high percentage of cells was killed. The surviving cells exhibited shattered chromosomes and multiple damage in the form of chromatid exchanges and breaks. ANF was not clastogenic nor did it induce SCEs in Chinese hamster ovary cells when incubated with microsomes form control rats or phenobarbital-treated rats. Moreover, NADPH was required for the clastogenic actions of ANF in the presence of 2,3,7,8-tetrachlorodibenzo(p)dioxin-induced microsomes. Analysis of the ANF metabolites by high-pressure liquid chromatography revealed that 2,3,7,8-tetrachlorodibenzo(p)dioxin-induced microsomes metabolized ANF to a much greater extent than control or phenobarbital-induced microsomes. Our results suggest that the clastogenic activity of ANF in Chinese hamster ovary cells is mediated by the cytochrome P-450 monooxygenase system.This publication has 15 references indexed in Scilit:
- Metabolism of α-naphthoflavone by rat, mouse, rabbit, and hamster liver microsomesToxicology and Applied Pharmacology, 1984
- 2,3,7,8-Tetrachlorodibenzo-p-dioxin receptors in wild type and variant mouse hepatoma cells. Nuclear location and strength of nuclear binding.Journal of Biological Chemistry, 1984
- Metabolism of alpha-naphthoflavone and beta-naphthoflavone by rat liver microsomes and highly purified reconstituted cytochrome P-450 systems.Journal of Biological Chemistry, 1983
- Induction of two immunochemically related rat liver cytochrome P-450 isozymes, cytochromes P-450c and P-450d, by structurally diverse xenobiotics.Journal of Biological Chemistry, 1983
- Reanalysis and clarification of the structures of α-naphthoflavone dihydrodiols formed by uninduced and induced rat liver microsomes from Charles River CD and Sprague-Dawley ratsCarcinogenesis: Integrative Cancer Research, 1983
- The influence of various enzyme inducers on the microsomal metabolism of 7,8-benzoflavoneCarcinogenesis: Integrative Cancer Research, 1982
- Chemically‐induced unscheduled DNA synthesis in primary rat hepatocyte cultures: A comparison with bacterial mutagenicity using 218 compoundsEnvironmental Mutagenesis, 1981
- METABOLISM OF ALPHA-NAPHTHOFLAVONE BY RAT-LIVER MICROSOMES1981
- Microsomal metabolites of the aryl hydrocarbon hydroxylase and tumour inhibitor 7,8-benzoflavoneCarcinogenesis: Integrative Cancer Research, 1981
- Stereospecific, high affinity binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin by hepatic cytosol. Evidence that the binding species is receptor for induction of aryl hydrocarbon hydroxylase.Journal of Biological Chemistry, 1976