Chemoprevention of heterocyclic amine-induced carcinogenesis by phenolic compounds in rats

被引:55
作者
Hirose, M
Takahashi, S
Ogawa, K
Futakuchi, M
Shirai, T
Shibutani, M
Uneyama, C
Toyoda, K
Iwata, H
机构
[1] Natl Inst Hlth Sci, Biol Safety Res Ctr, Div Pathol, Setagaya Ku, Tokyo 1588501, Japan
[2] Nagoya City Univ, Sch Med, Dept Pathol 1, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[3] Mitsubishi Chem Corp, Div Res & Dev, Kashima Res Ctr, Ibaraki, Japan
关键词
heterocyclic amine; antioxidants; chemoprevention; carcinogenesis; rat;
D O I
10.1016/S0304-3835(99)00120-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemopreventive effects of synthetic and naturally occurring antioxidants on heterocyclic amine (HCA)-induced rat carcinogenesis and mechanisms of inhibition were assessed. In a medium-term liver bioassay, combined treatment with 0.03% 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) and synthetic antioxidants such as 1-O-hexyl-2,3,5-trimethylhydroquinone (HTHQ), BHA, BHT, tert-butylhydroquinone (TBHQ) and propyl gallate, each at a dose of 0.25%, and troglitazone at doses 0.5 and 0.1%, potently inhibited development of glutathione S-transferase placental form (GST-P) positive foci as compared with MeIQx alone values. Of these antioxidants, HTHQ showed the greatest activity. Green tea catechins tended to inhibit GST-P positive foci development, while quercetin, rutin, curcumin, daidzin, ferulic acid and genistin all exerted significant enhancing effects. HTHQ also inhibited 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced colon carcinogenesis in a two stage colon carcinogenesis model using 1,2-dimethylhydrazine (DMH) as an initiator. Immunohistochemically detected PhIP-DNA adduct positive nuclei in the colon induced by continuous oral treatment with 0.02% PhIP for 2 weeks decreased by the combined treatment with 0.5 or 0.125% HTHQ. Methoxyresorfin O-demethylase activity in rat liver microsomes in vitro was clearly inhibited by the addition of HTHQ, BHA, BHT, TBHQ or propyl gallate, with particularly strong inhibition being observed in HTHQ. However, the CYP1A2 level in rat liver increased after oral treatment with HTHQ for 2 weeks. These results indicate that synthetic antioxidants, HTHQ in particular, is a very strong chemopreventor of HCA-induced carcinogenesis. It is suggested that depression of metabolic activation rather than antioxidant activity is responsible for the observed effect. However, other mechanisms, including the effects on phase II enzymes cannot be ruled out. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:173 / 178
页数:6
相关论文
共 18 条
[11]   SYNTHETIC ANTIOXIDANTS - BIOCHEMICAL ACTIONS AND INTERFERENCE WITH RADIATION, TOXIC COMPOUNDS, CHEMICAL MUTAGENS AND CHEMICAL CARCINOGENS [J].
KAHL, R .
TOXICOLOGY, 1984, 33 (3-4) :185-228
[12]  
KATO R, 1987, JPN J CANCER RES, V78, P297
[13]   INTAKE OF FRIED MEAT AND RISK OF CANCER - A FOLLOW-UP-STUDY IN FINLAND [J].
KNEKT, P ;
STEINECK, G ;
JARVINEN, R ;
HAKULINEN, T ;
AROMAA, A .
INTERNATIONAL JOURNAL OF CANCER, 1994, 59 (06) :756-760
[14]   CANCER RISK OF HETEROCYCLIC AMINES IN COOKED FOODS - AN ANALYSIS AND IMPLICATIONS FOR RESEARCH [J].
LAYTON, DW ;
BOGEN, KT ;
KNIZE, MG ;
HATCH, FT ;
JOHNSON, VM ;
FELTON, JS .
CARCINOGENESIS, 1995, 16 (01) :39-52
[15]   ACTIVATION AND DETOXICATION OF N-HYDROXY-TRP-P-2 BY GLUTATHIONE AND GLUTATHIONE TRANSFERASES [J].
SAITO, K ;
YAMAZOE, Y ;
KAMATAKI, T ;
KATO, R .
CARCINOGENESIS, 1983, 4 (12) :1551-1557
[16]  
Takahashi S, 1998, CANCER RES, V58, P4307
[17]   Presence of N-2-(deoxyguanosin-8-yl)-2-amino-3,8-demethylimidazo [4,5-f]quinoxaline (dG-C8-MeIQx) in human tissues [J].
Totsuka, Y ;
Fukutome, K ;
Takahashi, M ;
Takahashi, S ;
Tada, A ;
Sugimura, T ;
Wakabayashi, K .
CARCINOGENESIS, 1996, 17 (05) :1029-1034
[18]   CHARACTERIZATION OF DNA ADDUCTS FORMED INVITRO BY REACTION OF NORMAL-HYDROXY-2-AMINO-3-METHYLIMIDAZO[4,5-F]QUINOLINE AND NORMAL-HYDROXY-2-AMINO-3,8-DIMETHYLIMIDAZO[4,5-F]QUINOXALINE AT THE C-8 AND N-2 ATOMS OF GUANINE [J].
TURESKY, RJ ;
ROSSI, SC ;
WELTI, DH ;
LAY, JO ;
KADLUBAR, FF .
CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (04) :479-490