Induction of xenobiotic-metabolizing enzymes in hepatocytes by beta-naphthoflavone: Time-dependent changes in activities, protein and mRNA levels
Jazyk angličtina Země Polsko Médium print
Typ dokumentu časopisecké články
PubMed
29453911
DOI
10.2478/acph-2018-0005
PII: /j/acph.2018.68.issue-1/acph-2018-0005/acph-2018-0005.xml
Knihovny.cz E-zdroje
- Klíčová slova
- aryl hydrocarbon receptor (AhR), beta-naphthoflavone, mRNA-protein correlation, rat hepatocyte, time dependency,
- MeSH
- beta-naftoflavon metabolismus MeSH
- cytochrom P-450 CYP1A1 metabolismus MeSH
- cytochrom P-450 CYP1A2 metabolismus MeSH
- glutathiontransferasa metabolismus MeSH
- hepatocyty metabolismus MeSH
- játra metabolismus MeSH
- krysa rodu Rattus MeSH
- ligandy MeSH
- messenger RNA metabolismus MeSH
- NAD(P)H dehydrogenasa (chinon) metabolismus MeSH
- receptory aromatických uhlovodíků metabolismus MeSH
- xenobiotika metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- beta-naftoflavon MeSH
- cytochrom P-450 CYP1A1 MeSH
- cytochrom P-450 CYP1A2 MeSH
- glutathiontransferasa MeSH
- ligandy MeSH
- messenger RNA MeSH
- NAD(P)H dehydrogenasa (chinon) MeSH
- receptory aromatických uhlovodíků MeSH
- xenobiotika MeSH
In the present study, time-dependency of the induction effect of a selective inducer on the activity, protein and mRNA levels of cytochromes P450 1A1/2 (CYP1A1/2), NAD(P)H:quinone oxidoreductase 1 (NQO1) and glutathione S-transferases (GSTA), in primary culture of rat hepatocytes was tested and evaluated. To show the differences in responses of tested enzymes, the common aryl hydrocarbon receptor (AhR) ligand agonist, beta-naphthoflavone (BNF), was used. Induction of CYP1A1/2 by BNF was detected at all time intervals and at all levels (i.e., mRNA, protein, enzyme activity). Different responses of NQO1 and GSTA upon BNF treatment were observed. Our results demonstrate that the responses of different xenobiotic-metabolizing enzymes to the inducer vary in time and depend on the measured parameter. For these reasons, an induction study featuring only one-time interval treatment and/ or one parameter testing could produce misleading information.
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