Induction of murine intestinal and hepatic peroxiredoxin MSP23 by dietary butylated hydroxyanisole

被引:24
作者
Ishii, T
Itoh, K
Akasaka, J
Yanagawa, T
Takahashi, S
Yoshida, H
Bannai, S
Yamamoto, M
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Biochem, Tsukuba, Ibaraki 3058575, Japan
[2] Univ Tsukuba, Tsukuba Adv Res Alliance Ctr, Tsukuba, Ibaraki 3058575, Japan
[3] Univ Tsukuba, Inst Clin Sci, Dept Oral & Maxillofacial Surg, Tsukuba, Ibaraki 3058575, Japan
关键词
D O I
10.1093/carcin/21.5.1013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Feeding mice with 2(3)-t-butyl-4-hydroxyanisole (BHA) induces phase LT detoxifying enzymes that inhibit the action of carcinogens. We have found that dietary BHA induces intestinal and hepatic MSP23 (also called peroxiredoxin I), a stress-inducible antioxidant, in a manner similar to the induction of glutathione S-transferases (GSTs), The levels of MSP23 in the proximal intestine and liver, estimated by immunoblotting? increased approximately 1,9- and 1.3-fold, respectively, in mice fed a diet containing 0.7% (w/w) BHA for 7 days. The level of MSP23 mRNA in these tissues also increased more than 2-fold after mice mere fed BHA, suggesting that the induction of MSP23 is controlled at the transcription level. Immunostaining of the small intestine shows that MSP23 is expressed mainly in the columnar epithelial cells. The induction of MSP23 may be important to protect the cells and tissues against toxic electrophiles and reactive oxygen species.
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收藏
页码:1013 / 1016
页数:4
相关论文
共 23 条
[11]   Regulatory role for a novel human thioredoxin peroxidase in NF-κB activation [J].
Jin, DY ;
Chae, HZ ;
Rhee, SG ;
Jeang, KT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30952-30961
[12]   PRODUCTION OF REACTIVE OXYGEN SPECIES DUE TO METABOLIC-ACTIVATION OF BUTYLATED HYDROXYANISOLE [J].
KAHL, R ;
WEINKE, S ;
KAPPUS, H .
TOXICOLOGY, 1989, 59 (02) :179-194
[13]   Mammalian peroxiredoxin isoforms can reduce hydrogen peroxide generated in response to growth factors and tumor necrosis factor-α [J].
Kang, SW ;
Chae, HZ ;
Seo, MS ;
Kim, KH ;
Baines, IC ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (11) :6297-6302
[14]   ELEVATION OF CONJUGATION CAPACITY IN ISOLATED HEPATOCYTES FROM BHA-TREATED MICE [J].
MOLDEUS, P ;
DOCK, L ;
CHA, YN ;
BERGGREN, M ;
JERNSTROM, B .
BIOCHEMICAL PHARMACOLOGY, 1982, 31 (10) :1907-1910
[15]   Role of oxidants and antioxidants in the induction of AP-1, NF-kappa B, and glutathione S-transferase gene expression [J].
Pinkus, R ;
Weiner, LM ;
Daniel, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (23) :13422-13429
[16]   ROLE OF QUINONE-MEDIATED GENERATION OF HYDROXYL RADICALS IN THE INDUCTION OF GLUTATHIONE-S-TRANSFERASE GENE-EXPRESSION [J].
PINKUS, R ;
WEINER, LM ;
DANIEL, V .
BIOCHEMISTRY, 1995, 34 (01) :81-88
[17]  
PRESTERA T, 1993, ADV ENZYME REGUL, V33, P281
[18]  
Primiano T, 1997, Adv Pharmacol, V38, P293
[19]   Thioredoxin peroxidase (natural killer enhancing factor) regulation of activator protein-1 function in endothelial cells [J].
Shau, H ;
Huang, ACJ ;
Faris, M ;
Nazarian, R ;
de Vellis, J ;
Chen, W .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 249 (03) :683-686
[20]  
WATTENBERG LW, 1972, JNCI-J NATL CANCER I, V48, P1425