Treatment of rats with the peroxisome proliferator ciprofibrate results in increased liver NF-kappa B activity

被引:52
作者
Li, Y
Leung, LK
Glauert, HP
Spear, BT
机构
[1] UNIV KENTUCKY,COLL MED,DEPT MICROBIOL & IMMUNOL,LEXINGTON,KY 40536
[2] UNIV KENTUCKY,COLL MED,DEPT LAB MED & PATHOL,LEXINGTON,KY 40536
[3] UNIV KENTUCKY,COLL MED,DEPT FOOD SCI & NUTR,LEXINGTON,KY 40536
[4] UNIV KENTUCKY,COLL MED,NUTR SCI PROGRAM,LEXINGTON,KY 40536
[5] UNIV KENTUCKY,COLL MED,GRAD CTR TOXICOL,LEXINGTON,KY 40536
关键词
D O I
10.1093/carcin/17.11.2305
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nuclear factor kappa B (NF-kappa B) is an important stress-induced transcription factor in many cell types, including hepatocytes. Previous studies have shown that reactive oxygen species, including hydrogen peroxide, are potent activators of NF-kappa B. Peroxisome proliferators are a group of rodent chemical carcinogens that have been proposed to act by increasing reactive oxygen in the liver. These results led us to consider whether peroxisome proliferators would increase NF-kappa B activity in the liver, Here we demonstrate that rats fed diets containing the peroxisome proliferator ciprofibrate exhibit increased hepatic NF-kappa B DNA-binding activity, This observation suggests that NF-kappa B may contribute, in part, to peroxisome proliferator-mediated changes in the liver.
引用
收藏
页码:2305 / 2309
页数:5
相关论文
共 58 条
[1]   REDUCTION OF RAT-LIVER ENDOPLASMIC-RETICULUM CA2+-ATPASE ACTIVITY AND MOBILIZATION OF HEPATIC INTRACELLULAR CALCIUM BY CIPROFIBRATE, A PEROXISOME PROLIFERATOR [J].
BENNETT, AM ;
WILLIAMS, GM .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (03) :595-605
[2]  
BOGES HK, 1994, TOXICOL APPL PHARM, V126, P233
[3]   ELEVATED 8-HYDROXYDEOXYGUANOSINE IN HEPATIC DNA OF RATS FOLLOWING EXPOSURE TO PEROXISOME PROLIFERATORS - RELATIONSHIP TO CARCINOGENESIS AND NUCLEAR-LOCALIZATION [J].
CATTLEY, RC ;
GLOVER, SE .
CARCINOGENESIS, 1993, 14 (12) :2495-2499
[4]   ASSOCIATION OF PERSISTENT PEROXISOME PROLIFERATION AND OXIDATIVE INJURY WITH HEPATOCARCINOGENICITY IN FEMALE F344 RATS FED DI(2-ETHYLHEXYL)PHTHALATE FOR 2 YEARS [J].
CATTLEY, RC ;
CONWAY, JG ;
POPP, JA .
CANCER LETTERS, 1987, 38 (1-2) :15-22
[5]  
CHERKAOUIMALKI M, 1990, BIOCHEM BIOPH RES CO, V173, P855
[6]   TRANSFORMATION OF MAMMALIAN-CELLS BY OVEREXPRESSING H2O2-GENERATING PEROXISOMAL FATTY ACYL-COA OXIDASE [J].
CHU, S ;
HUANG, Q ;
ALVARES, K ;
YELDANDI, AV ;
RAO, MS ;
REDDY, JK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (15) :7080-7084
[7]   RELATIONSHIP OF OXIDATIVE DAMAGE TO THE HEPATOCARCINOGENICITY OF THE PEROXISOME PROLIFERATORS DI(2-ETHYLHEXYL)PHTHALATE AND WY-14,643 [J].
CONWAY, JG ;
TOMASZEWSKI, KE ;
OLSON, MJ ;
CATTLEY, RC ;
MARSMAN, DS ;
POPP, JA .
CARCINOGENESIS, 1989, 10 (03) :513-519
[8]   Effect of the hepatocarcinogenic peroxisome proliferator Wy-14,643 in vivo: No increase in ethane exhalation or hepatic conjugated dienes [J].
Conway, JG ;
Popp, JA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 135 (02) :229-236
[9]  
COSTA RH, 1994, LIVER GENE TRANSCRIP, P183
[10]  
CRESSMAN DE, 1994, J BIOL CHEM, V269, P30429