Detection of Initiation Activity of 1,2-Dimethylhydrazine in in vivo Medium-Term Liver Initiation Assay System using 4-Week-Old Rats without Hepatocellular Proliferative Stimuli during the Test Chemical Treatment Period

被引:3
作者
Asaoka, Yoshiji [2 ,4 ]
Sakai, Hiroki [1 ,2 ]
Hirata, Akihiro [3 ]
Sasaki, Jun [2 ,5 ]
Goryo, Masanobu [4 ,5 ]
Miyamoto, Yohei [4 ]
Yanai, Tokuma [1 ,2 ]
Masegi, Toshiaki [1 ,2 ]
Okada, Kosuke [2 ,5 ]
机构
[1] Gifu Univ, Lab Vet Pathol, Fac Appl Biol Sci, Gifu 5011193, Japan
[2] Gifu Univ, Pathogen Vet Sci, United Grad Sch Vet Sci, Gifu 5011193, Japan
[3] Gifu Univ, Div Anim Expt, Life Sci Res Ctr, Gifu 5011193, Japan
[4] Toray Industries Ltd, Lab Toxicol & Pharmacokinet, Pharmaceut Res Labs, Kanagawa 2488555, Japan
[5] Iwate Univ, Dept Vet Pathol, Fac Agr, Morioka, Iwate 0208555, Japan
关键词
1,2-dimethylhydrazine (DMH)Introduction; carcinogenesis; GST-P-positive cell foci; liver; rat; LIQUID-CHROMATOGRAPHIC METHOD; GLUTATHIONE S-TRANSFERASE; CELL FOCI; PARTIAL-HEPATECTOMY; N-NITROSODIMETHYLAMINE; NON-HEPATOCARCINOGEN; INDUCTION; CARCINOGENESIS; MICROSOMES; CYTOCHROME-P450;
D O I
10.1292/jvms.09-0297
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
We have developed ail in vivo medium-term liver initiation assay system to detect initiation activities of chemicals of) multiorgan carcinogenesis. However, cell proliferation Stimuli during the test chemical treatment period, required in the previously used assay models using adult rats, are laborious; moreover, those cause decrease of hepatic metabolic enzymes and psychological and physical discomfort to animals resulting in inaccurate interpretation. Therefore, we investigated the utility of another in vivo medium-term liver initiation assay model using 4-week-old rats without the cell proliferation Stimuli. In this study, we confirmed that 4-week-old and 4.5-week-old male rats have high hepatocyte proliferation activity and similar enzyme activities of hepatic Cytochrome P450 subtypes as compared with 8-week-old male rats. Next, the in vivo medium-term liver initiation assay model using 4-week-old rats without cell proliferation stimuli was evaluated for the detection of the initiation activity of 1,2-dimethylhydrazine (DMH), which is a well-known genotoxic carcinogen. Four-week-old rats were orally administered DMH (single dose, 4 or 16 mg/kg; or 4-day repeat, I or 4 mg/kg); subsequently, these rats were treated promotion treatment consisted of administration of 2-acetylaminofluorene and carbon tetrachloride. Four weeks after the first DMH administration, the glutathione S-transferase placental form (GST-P)-positive foci induced by DMH in the liver was measured immunohistochemically. The inductions of GST-P-positive foci in all DMH-treated groups were dose-dependent, duration-dependent and significantly higher than that in non-DMH-treated group. From these results, our assay model was detected the initiation activity of DMH simply, and would be useful to evaluate the carcinogenicity of chemicals.
引用
收藏
页码:43 / 53
页数:11
相关论文
共 58 条
[1]   The causes and prevention of cancer: The role of environment [J].
Ames, BN ;
Gold, LS .
BIOTHERAPY, 1998, 11 (2-3) :205-220
[2]   Intraperitoneal injection of D-galactosamine provides a potent cell proliferation stimulus for the detection of initiation activities of chemicals in rat liver [J].
Asaoka, Y ;
Sakai, H ;
Takahashi, N ;
Hirata, A ;
Tsukamoto, T ;
Yamamoto, M ;
Yanai, T ;
Masegi, T ;
Tatematsu, M .
JOURNAL OF APPLIED TOXICOLOGY, 2005, 25 (06) :554-561
[3]   AGE-RELATED AND SEX-RELATED EXPRESSION OF YTOCHROMES-P450F AND P450G IN RAT-LIVER [J].
BANDIERA, S ;
RYAN, DE ;
LEVIN, W ;
THOMAS, PE .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 248 (02) :658-676
[4]   CYTOCHROME-P450 SPECIFICITIES OF ALKOXYRESORUFIN O-DEALKYLATION IN HUMAN AND RAT-LIVER [J].
BURKE, MD ;
THOMPSON, S ;
WEAVER, RJ ;
WOLF, CR ;
MAYER, RT .
BIOCHEMICAL PHARMACOLOGY, 1994, 48 (05) :923-936
[5]   INITIATION OF CHEMICAL CARCINOGENESIS REQUIRES CELL-PROLIFERATION [J].
CAYAMA, E ;
TSUDA, H ;
SARMA, DSR ;
FARBER, E .
NATURE, 1978, 275 (5675) :60-62
[6]   CELL-PROLIFERATION IN CARCINOGENESIS [J].
COHEN, SM ;
ELLWEIN, LB .
SCIENCE, 1990, 249 (4972) :1007-1011
[7]   A UNIQUE PATTERN OF HEPATOCYTE PROLIFERATION IN F344 RATS FOLLOWING LONG-TERM EXPOSURES TO LOW-LEVELS OF A CHEMICAL-MIXTURE OF GROUNDWATER CONTAMINANTS [J].
CONSTAN, AA ;
YANG, RSH ;
BAKER, DC ;
BENJAMIN, SA .
CARCINOGENESIS, 1995, 16 (02) :303-310
[8]   MEAT, COOKING METHODS AND COLORECTAL-CANCER - A CASE-REFERENT STUDY IN STOCKHOLM [J].
DEVERDIER, MG ;
HAGMAN, U ;
PETERS, RK ;
STEINECK, G ;
OVERVIK, E .
INTERNATIONAL JOURNAL OF CANCER, 1991, 49 (04) :520-525
[9]   Ontogeny of hepatic CYP1A2 and CYP2E1 expression in rat [J].
Elbarbry, Fawzy A. ;
McNamara, Patrick J. ;
Alcorn, Jane .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2007, 21 (01) :41-50
[10]   Comparison of different initiation protocols in the resistant hepatocyte model [J].
Espandiari, P ;
Robertson, LW ;
Srinivasan, C ;
Glauert, HP .
TOXICOLOGY, 2005, 206 (03) :373-381