TY - JOUR
T1 - Gene expression of detoxifying enzymes in AhR and Nrf2 compound null mutant mouse
AU - Noda, Shuhei
AU - Harada, Nobuhiko
AU - Hida, Azumi
AU - Fujii-Kuriyama, Yoshiaki
AU - Motohashi, Hozumi
AU - Yamamoto, Masayuki
N1 - Funding Information:
We are grateful to Drs. Vincent Kelley, Tomonori Hosoya, Jun-sei Mimura, and Satoru Takahashi for discussion, and Masahiko Negishi for CYP2B10 cDNA. We thank Ms. Naomi Kaneko for histological analysis and Reiko Kawai for mouse breeding. This work was supported by grants from ERATO (M.Y.), the Ministry of Education, Science, Sports and Culture (H.M. and M.Y.), JSPS-RFTF (M.Y.), CREST (M.Y. and Y.F.-K.), PROBRAIN (H.M.), and Special Coordination Fund for Promoting Science and Technology (H.M.).
PY - 2003/3/28
Y1 - 2003/3/28
N2 - 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.
AB - 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.
KW - 3-Methylchoranthrene
KW - Butylated hydroxyanisole
KW - Gene knockout mouse
KW - Phase I enzymes
KW - Phase II enzymes
KW - Phenobarbital
KW - Xenobiotics
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U2 - 10.1016/S0006-291X(03)00306-1
DO - 10.1016/S0006-291X(03)00306-1
M3 - Article
C2 - 12646173
AN - SCOPUS:0037470745
SN - 0006-291X
VL - 303
SP - 105
EP - 111
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -