Gene expression of detoxifying enzymes in AhR and Nrf2 compound null mutant mouse

被引:40
作者
Noda, S
Harada, N
Hida, A
Fujii-Kuriyama, Y
Motohashi, H
Yamamoto, M
机构
[1] Univ Tsukuba, Ctr Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 3058577, Japan
[2] Japan Sci & Technol Corp, ERATO, Environm Response Project, Tsukuba, Ibaraki 3058577, Japan
基金
日本学术振兴会;
关键词
xenobiotics; phase I enzymes; phase II enzymes; gene knockout mouse; 3-methylchoranthrene; butylated hydroxyanisole; phenobarbital;
D O I
10.1016/S0006-291X(03)00306-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mousemodel, 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. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:105 / 111
页数:7
相关论文
共 30 条
  • [1] Accelerated DNA adduct formation in the lung of the Nrf2 knockout mouse exposed to diesel exhaust
    Aoki, Y
    Sato, H
    Nishimura, N
    Takahashi, S
    Itoh, K
    Yamamoto, M
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 173 (03) : 154 - 160
  • [2] BAYLY AC, 1993, J CELL SCI, V104, P307
  • [3] Recruitment of the NCoA/SRC-1/p160 family of transcriptional coactivators by the aryl hydrocarbon receptor/aryl hydrocarbon receptor nuclear translocator complex
    Beischlag, TV
    Wang, S
    Rose, DW
    Torchia, J
    Reisz-Porszasz, S
    Muhammad, K
    Nelson, WE
    Probst, MR
    Rosenfeld, MG
    Hankinson, O
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (12) : 4319 - 4333
  • [4] CHUNG I, 1995, MOL PHARMACOL, V47, P677
  • [5] CUMMINGS SW, 1985, CANCER RES, V45, P5617
  • [6] High sensitivity of Nrf2 knockout mice to acetaminophen hepatotoxicity associated with decreased expression of ARE-regulated drug metabolizing enzymes and antioxidant genes
    Enomoto, A
    Itoh, K
    Nagayoshi, E
    Haruta, J
    Kimura, T
    O'Connor, T
    Harada, T
    Yamamoto, M
    [J]. TOXICOLOGICAL SCIENCES, 2001, 59 (01) : 169 - 177
  • [7] FAVREAU LV, 1991, J BIOL CHEM, V266, P4556
  • [8] IMMUNE-SYSTEM IMPAIRMENT AND HEPATIC-FIBROSIS IN MICE LACKING THE DIOXIN-BINDING AH RECEPTOR
    FERNANDEZSALGUERO, P
    PINEAU, T
    HILBERT, DM
    MCPHAIL, T
    LEE, SST
    KIMURA, S
    NEBERT, DW
    RUDIKOFF, S
    WARD, JM
    GONZALEZ, FJ
    [J]. SCIENCE, 1995, 268 (5211) : 722 - 726
  • [9] XENOBIOTIC-INDUCIBLE EXPRESSION OF MURINE GLUTATHIONE-S-TRANSFERASE YA-SUBUNIT GENE IS CONTROLLED BY AN ELECTROPHILE-RESPONSIVE ELEMENT
    FRILING, RS
    BENSIMON, A
    TICHAUER, Y
    DANIEL, V
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) : 6258 - 6262
  • [10] A DNA-BINDING FACTOR SPECIFIC FOR XENOBIOTIC RESPONSIVE ELEMENTS OF P-450C GENE EXISTS AS A CRYPTIC FORM IN CYTOPLASM - ITS POSSIBLE TRANSLOCATION TO NUCLEUS
    FUJISAWASEHARA, A
    YAMANE, M
    FUJIIKURIYAMA, Y
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) : 5859 - 5863