The environmental pollutant and carcinogen 3-nitrobenzanthrone and its human metabolite 3-aminobenzanthrone are potent inducers of rat hepatic cytochromes P450 1A1 and -1A2 and NAD(P)H:quinone oxidoreductase
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
16714372
DOI
10.1124/dmd.106.009373
PII: S0090-9556(24)03577-3
Knihovny.cz E-zdroje
- MeSH
- adukty DNA MeSH
- benz(a)anthraceny farmakologie MeSH
- enzymová indukce MeSH
- jaterní mikrozomy účinky léků enzymologie MeSH
- játra účinky léků enzymologie MeSH
- karcinogeny farmakologie MeSH
- králíci MeSH
- krysa rodu Rattus MeSH
- látky znečišťující životní prostředí farmakologie MeSH
- lidé MeSH
- messenger RNA analýza MeSH
- NAD(P)H dehydrogenasa (chinon) biosyntéza MeSH
- potkani Wistar MeSH
- systém (enzymů) cytochromů P-450 biosyntéza genetika MeSH
- zvířata MeSH
- Check Tag
- králíci MeSH
- krysa rodu Rattus MeSH
- lidé MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 3-aminobenzanthrone MeSH Prohlížeč
- 3-nitrobenzanthrone MeSH Prohlížeč
- adukty DNA MeSH
- benz(a)anthraceny MeSH
- karcinogeny MeSH
- látky znečišťující životní prostředí MeSH
- messenger RNA MeSH
- NAD(P)H dehydrogenasa (chinon) MeSH
- NQO1 protein, rat MeSH Prohlížeč
- systém (enzymů) cytochromů P-450 MeSH
3-Nitrobenzanthrone (3-NBA), a suspected human carcinogen occurring in diesel exhaust and air pollution, and its human metabolite 3-aminobenzanthrone (3-ABA) were investigated for their ability to induce biotransformation enzymes in rat liver and the influence of such induction on DNA adduct formation by the compounds. Rats were treated (i.p.) with 0.4, 4, or 40 mg/kg body weight 3-NBA or 3-ABA. When hepatic cytosolic fractions from rats treated with 40 mg/kg body weight 3-NBA or 3-ABA were incubated with 3-NBA, DNA adduct formation, measured by 32P-postlabeling analysis, was 10-fold higher in incubations with cytosols from pretreated rats than with controls. The increase in 3-NBA-derived DNA adduct formation corresponded to a dose-dependent increase in protein levels and enzymatic activity of NAD(P)H:quinone oxidoreductase (NQO1). NQO1 is the major enzyme reducing 3-NBA in human and rat livers. Incubations of 3-ABA with hepatic microsomes of rats treated with 3-NBA or 3-ABA (40 mg/kg body weight) led to as much as a 12-fold increase in 3-ABA-derived DNA adduct formation compared with controls. The observed stimulation of DNA adduct formation by both compounds was attributed to their potential to induce protein expression and enzymatic activity of cytochromes P450 1A1 and/or -1A2 (CYP1A1/2), the major enzymes responsible for 3-ABA activation in human and rat livers. Collectively, these results demonstrate for the first time, to our knowledge, that by inducing hepatic NQO1 and CYP1A1/2, both 3-NBA and 3-ABA increase the enzymatic activation of these two compounds to reactive DNA adduct-forming species, thereby enhancing their own genotoxic potential.
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