DNA adduct formation and 7-ethoxyresorufin O-deethylase induction in primary culture of rainbow trout hepatocytes exposed to benzo[a]pyrene

TOXICOLOGY IN VITRO(1992)

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摘要
The formation of DNA adducts, using the P-32-postlabelling assay, and induction of 7-ethoxy-resorufin O-deethylase (EROD) were investigated in a primary culture of rainbow trout hepatocytes exposed to benzo[a]pyrene (B[a]P). Concentrations of 0.1 and 1 muM-B[a]P were shown to induce EROD whereas 10 muM was an inhibitory concentration. DNA adducts were detected for 12 hr to 72 hr after exposure to 1 muM-B[a]P whereas EROD activity was increased 36 hr after treatment. The pattern of adducts was shown to be identical to that obtained after B[a]P treatment of rainbow trout in vivo, as demonstrated by co-chromatography of the adducts. Pre-exposure of hepatocytes for 48 hr to beta-naphthoflavone (betaNF) and subsequent 24-hr exposure to 1 muM-B[a]P did not lead to increased DNA adduct formation although betaNF treatment led to a 3.4-fold induction of EROD activity at the time of B[a]P addition. This study suggests that primary culture of rainbow trout hepatocytes provides a suitable method for studying DNA adduct formation and its modulating factors in vitro.
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pei,dmso,ahh,8-diol 9,p -450,βnf,benzo[ a ]pyrene,pah,7-ethoxyresorufin o -deethylase,β-naphthoflavone,erod,polyethyleneimine,polycyclic aromatic hydrocarbon,cytochrome p -450,b[ a ]p,10-epoxide,aryl hydrocarbon hydroxylase,dimethyl sulphoxide,b[ a ]p 7,bpde
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