Cyclophosphamide induces mRNA, protein and enzyme activity of cytochrome P450 in rat

被引:14
|
作者
Xie, H
Afsharian, P
Terelius, Y
Mirghani, RA
Yasar, Ü
Hagbjörk, AL
Lundgren, S
Hu, Y
Rane, A
Hassan, M [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst,Novum, KFC,Dept Med,Div Hematol, Hematol Lab, S-14186 Huddinge, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Lab Med, Div Clin Pharmacol, S-14186 Huddinge, Sweden
[3] AstraZeneca R&D Sodertalje, Dept Res DMPK, Sodertalje, Sweden
关键词
cyclophosphamide; cytochrome P450; induction; pharmacogenetic; CYP2B; CYB2C; CYP3A;
D O I
10.1080/00498250500057369
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of cyclophosphamide (CPA) on CYP enzymes in vivo and its auto induction in rat were investigated in Wistar/Fu male rats at a single dose ( 40 or 200 mg kg(-1)) or as repeated dose of 200 mg kg(-1) CPA. After a single dose of CPA, mRNAs of CYPs 2B1, 2B2, 3A2, 2C11 were significantly induced up to 220-, 6.7-, 5.0- and 5.8-fold at the low dose CPA, and 4800-, 52-, 22- and 2.5-fold at the high dose. CYP2B1/2 and CYP3A proteins were increased by 4- and 2-fold ( low dose) and by 28- and 1.7-fold ( high dose). CYP2C11 protein levels were not altered. Microsomal activities of CYP2B, CYP3A and 2C11 were increased by 2-, 1.8- and 1.3-fold at low dose CPA, and 3.2-, 1.7- and 1.6-fold at high dose. A significant (p< 0.05) decrease in CPA concentration and a significant ( p < 0.05) increase in 4-OH-CPA levels were observed with repeated administration of CPA. Acute induction effect on CYP2B1, 2B2, 2C11 and 3A2 and a substantial up regulation of CYP2B1 mRNA were observed after a single dose of CPA, auto induction was observed by repeated administration.
引用
收藏
页码:239 / 251
页数:13
相关论文
共 50 条
  • [31] The impact of intrauterine growth restriction on cytochrome P450 enzyme expression and activity
    McBride, Grace M.
    Wiese, Michael D.
    Soo, Jia Yin
    Darby, Jack R. T.
    Berry, Mary J.
    Varcoe, Tamara J.
    Morrison, Janna L.
    PLACENTA, 2020, 99 : 50 - 62
  • [32] A new technique for assaying cytochrome P450 enzyme activity in a single cell
    Taira Z.
    Yamase D.
    Ueda Y.
    Cell Biology and Toxicology, 2007, 23 (3) : 143 - 151
  • [33] Cytochrome P450 dependent enzyme activity in antigen presenting cells.
    Merk, HF
    Schenk, V
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (01) : 1999 - 1999
  • [34] Effect of cardiopulmonary bypass on cytochrome P450 enzyme activity: implications for pharmacotherapy
    Adiraju, Santosh Kumar Sreevatsav
    Shekar, Kiran
    Fraser, John F.
    Smith, Maree T.
    Ghassabian, Sussan
    DRUG METABOLISM REVIEWS, 2018, 50 (02) : 109 - 124
  • [35] Cytochrome P450: taming a wild type enzyme
    Jung, Sang Taek
    Lauchli, Ryan
    Arnold, Frances H.
    CURRENT OPINION IN BIOTECHNOLOGY, 2011, 22 (06) : 809 - 817
  • [36] Characterization of THLE-Cytochrome P450 (P450) Cell Lines: Gene Expression Background and Relationship to P450-Enzyme Activity
    Soltanpour, Yalda
    Hilgendorf, Constanze
    Ahlstrom, Marie M.
    Foster, Alison J.
    Kenna, J. Gerry
    Petersen, Anne
    Ungell, Anna-Lena
    DRUG METABOLISM AND DISPOSITION, 2012, 40 (11) : 2054 - 2058
  • [37] Crystal structure of a human cytochrome P450 enzyme
    Jhoti, H
    Williams, P
    Ward, A
    Cosme, J
    DRUG METABOLISM REVIEWS, 2002, 34 : 10 - 10
  • [38] Impact of Cytochrome P450 Enzyme on Fruit Quality
    Minerdi, Daniela
    Sabbatini, Paolo
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (13)
  • [39] From electrochemistry to enzyme kinetics of cytochrome P450
    Shumyantseva, Victoria V.
    Kuzikov, Alexey V.
    Masamrekh, Rami A.
    Bulko, Tatiana V.
    Archakov, Alexander I.
    BIOSENSORS & BIOELECTRONICS, 2018, 121 : 192 - 204
  • [40] Structural diversity of cytochrome P450 enzyme system
    Omura, Tsuneo
    JOURNAL OF BIOCHEMISTRY, 2010, 147 (03): : 297 - 306