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Gene expression of detoxifying enzymes in AhR and Nrf2 compound null mutant mouse
- Source :
- Biochemical and Biophysical Research Communications. 303:105-111
- Publication Year :
- 2003
- Publisher :
- Elsevier BV, 2003.
-
Abstract
- The arylhydrocarbon receptor (AhR) regulates the expression of cytochrome P450 (CYP)-1 gene family members which catalyze xenobiotic Phase I metabolism, while Nrf2 exerts the concerted regulation of Phase II enzyme genes. We generated AhR and Nrf2 compound null mutant mice to examine the integrated function of AhR- and Nrf2-regulated enzymes in detoxification. Furthermore, we used this mouse model, by administering three different classes of chemical inducers, to examine how xenobiotic metabolism may be influenced in the absence of signals transduced by AhR or Nrf2. The compound mutant mice responded only weakly to AhR ligand or Phase II inducer, while they displayed a clear response to phenobarbital, an inducer of the CYP2B family through another, unrelated transcription factor. Here, we report an initial characterization of the AhR-Nrf2 double mutant mice, which may serve as a simplified bioassay system to evaluate xenobiotic toxicity and metabolic biotransformation of various drugs and environmental chemicals.
- Subjects :
- Male
Time Factors
NF-E2-Related Factor 2
Mutant
Biophysics
Butylated Hydroxyanisole
Mice, Transgenic
Ligands
Biochemistry
Antioxidants
Catalysis
Mice
chemistry.chemical_compound
Gene expression
Animals
Gene family
Inducer
Molecular Biology
Transcription factor
Mice, Knockout
biology
Cytochrome P450
Cell Biology
respiratory system
Molecular biology
Cell biology
DNA-Binding Proteins
Models, Chemical
Receptors, Aryl Hydrocarbon
chemistry
Phenobarbital
Mutation
Carcinogens
Trans-Activators
biology.protein
Female
Xenobiotic
Drug metabolism
Methylcholanthrene
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 303
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....ddad68388f0e1c2590c33bb2ca5be722
- Full Text :
- https://doi.org/10.1016/s0006-291x(03)00306-1