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 ind...
International audienceThyroxine (T(4))-UDP-glucuronosyltransferase (UGT) activity was measured direc...
1. We review here the molecular mechanisms underlying the xenobiotic induction of genes encoding cyt...
a-Naphthoflavone (aNF) is a weak aryl hydrocarbon (Ah) receptor agonist and inhibits the induction o...
In the present study, time-dependency of the induction effect of a selective inducer on the activity...
Background and objectives: Drug-drug interactions have became an important issue in health care. Sin...
The aim of this investigation was to define the in vitro conditions necessary to support cytochrome ...
In the last decade, hydroxycinnamic acids (HCA) have gained increasing attention from researchers du...
dissertationThe nature of extent of drug metabolizing enzyme induction by exogenous compounds is oft...
Introduction. The constitutive expression of major drug metabolizing enzymes like cytochromes P450 (...
1) Phenobarbitone (PB) was administered to male C3H/He and C57B1/6 strain mice (high and low inciden...
Species differences exist in the induction response of CYP3A genes to xenobiotics, and these are pro...
Phase I and Phase II metabolizing enzymes assist in the removal of endogenous and exogenous chemical...
A mechanism of action of chemopreventive glucosinolates/isothiocyanates, established largely in vitr...
Constitutive androstane receptor (CAR) and peroxisome proliferator activated receptor (PPAR)α are tr...
Drug-induced liver injury (DILI) is a common reason for withdrawal of candidate drugs from clinical ...
International audienceThyroxine (T(4))-UDP-glucuronosyltransferase (UGT) activity was measured direc...
1. We review here the molecular mechanisms underlying the xenobiotic induction of genes encoding cyt...
a-Naphthoflavone (aNF) is a weak aryl hydrocarbon (Ah) receptor agonist and inhibits the induction o...
In the present study, time-dependency of the induction effect of a selective inducer on the activity...
Background and objectives: Drug-drug interactions have became an important issue in health care. Sin...
The aim of this investigation was to define the in vitro conditions necessary to support cytochrome ...
In the last decade, hydroxycinnamic acids (HCA) have gained increasing attention from researchers du...
dissertationThe nature of extent of drug metabolizing enzyme induction by exogenous compounds is oft...
Introduction. The constitutive expression of major drug metabolizing enzymes like cytochromes P450 (...
1) Phenobarbitone (PB) was administered to male C3H/He and C57B1/6 strain mice (high and low inciden...
Species differences exist in the induction response of CYP3A genes to xenobiotics, and these are pro...
Phase I and Phase II metabolizing enzymes assist in the removal of endogenous and exogenous chemical...
A mechanism of action of chemopreventive glucosinolates/isothiocyanates, established largely in vitr...
Constitutive androstane receptor (CAR) and peroxisome proliferator activated receptor (PPAR)α are tr...
Drug-induced liver injury (DILI) is a common reason for withdrawal of candidate drugs from clinical ...
International audienceThyroxine (T(4))-UDP-glucuronosyltransferase (UGT) activity was measured direc...
1. We review here the molecular mechanisms underlying the xenobiotic induction of genes encoding cyt...
a-Naphthoflavone (aNF) is a weak aryl hydrocarbon (Ah) receptor agonist and inhibits the induction o...