CHEMOPREVENTIVE EFFECTS OF BETA-CAROTENE, ALPHA-TOCOPHEROL AND 5 NATURALLY-OCCURRING ANTIOXIDANTS ON INITIATION OF HEPATOCARCINOGENESIS BY 2-AMINO-3-METHYLIMIDAZO[4,5-F]QUINOLINE IN THE RAT

被引:107
作者
TSUDA, H
UEHARA, N
IWAHORI, Y
ASAMOTO, M
IIGO, M
NAGAO, M
MATSUMOTO, K
ITO, M
HIRONO, I
机构
[1] NATL CANC CTR, RES INST, DIV CARCINOGENESIS, CHUO KU, TOKYO 104, JAPAN
[2] FUJITA HLTH UNIV, SCH MED, DEPT PATHOL, TOYOAKE, AICHI 47011, JAPAN
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1994年 / 85卷 / 12期
关键词
CHEMOPREVENTION; HEPATOCARCINOGENESIS; INITIATION; ANTIOXIDANT;
D O I
10.1111/j.1349-7006.1994.tb02932.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inhibitory effects of naturally occurring antioxidants on the initiation stage of hepatocarcinogenesis were studied. Group 1 rats were given a diet containing beta-carotene (beta-CT, 0.02%), alpha-tocopherol (alpha-TP, 1.5%), glutathione (GLT, 5%), vanillin (VNL, 1%), quercetin (QCT, 1%) or ellagic acid (ELA, 1%), or 3 doses of diallyl sulfide (DAS, 200 mg/kg, i.g.) over an 8-day period. On day 7, the animals received a single dose of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ, 100 mg/kg, i.g.), 12 h after two-thirds partial hepatectomy for initiation and 2 weeks thereafter, were placed on promotion regimen comprising phenobarbital (0.05% in diet) and a single dose of D-galactosamine (100 mg/kg, i.p.). Groups 2 and 3 were treated as described for Group 1, but without test material or IQ, respectively. Survivors were killed at week 11 and antioxidant influence was assessed by comparing values for preneoplastic glutathione S-transferase placental form-positive (GST-P+) foci between Groups 1 and 2. All lesions larger than 70 mu m in diameter consisting of approximately 5 cells in cross section were counted. Numbers of GST-P+ foci/cm(2) in Group 1 were: beta-CT, 7,99; alpha-TP, 8.21; GLT, 9.71; DAS, 10.37; VNL, 10,57; QCT, 11.1; ELA, 12.5 (n=11-15). All, except ELA, showed a significant decrease as compared with the Group 2 value of 14.54 (n=15). Only beta-CT showed a significant decrease for the area value. This is the first report to show that beta-CT, alpha-TP, GLT, DAS, VNL, QCT exert inhibitory effects on initiation of hepatocarcinogenesis by the food carcinogen IQ, suggesting that these antioxidants might find application as chemopreventive agents. Furthermore, the current protocol proved practical for the assessment of chemopreventive agents within 11 weeks, a relatively short period.
引用
收藏
页码:1214 / 1219
页数:6
相关论文
共 52 条
[1]   DIETARY CARCINOGENS AND ANTICARCINOGENS - OXYGEN RADICALS AND DEGENERATIVE DISEASES [J].
AMES, BN .
SCIENCE, 1983, 221 (4617) :1256-1264
[2]   MUTAGEN ACTIVATION BY CDNA-EXPRESSED P1450, P3450, AND P450A [J].
AOYAMA, T ;
GONZALEZ, FJ ;
GELBOIN, HV .
MOLECULAR CARCINOGENESIS, 1989, 1 (04) :253-259
[3]   PROTECTIVE ROLE OF AQUEOUS TURMERIC EXTRACT AGAINST MUTAGENICITY OF DIRECT-ACTING CARCINOGENS AS WELL AS BENZO[A]PYRENE-INDUCED GENOTOXICITY AND CARCINOGENICITY [J].
AZUINE, MA ;
KAYAL, JJ ;
BHIDE, SV .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1992, 118 (06) :447-452
[4]   BETA-CAROTENE - AN UNUSUAL TYPE OF LIPID ANTIOXIDANT [J].
BURTON, GW ;
INGOLD, KU .
SCIENCE, 1984, 224 (4649) :569-573
[5]   INITIATION OF CHEMICAL CARCINOGENESIS REQUIRES CELL-PROLIFERATION [J].
CAYAMA, E ;
TSUDA, H ;
SARMA, DSR ;
FARBER, E .
NATURE, 1978, 275 (5675) :60-62
[6]  
CRADDOCK VM, 1976, LIVER CELL CANCER, P153
[7]   A COMPARISON OF TOCOPHEROL AND TOCOTRIENOL FOR THE CHEMOPREVENTION OF CHEMICALLY-INDUCED RAT MAMMARY-TUMORS [J].
GOULD, MN ;
HAAG, JD ;
KENNAN, WS ;
TANNER, MA ;
ELSON, CE .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 53 (04) :S1068-S1070
[8]   INHIBITION OF 2-AMINO-3-METHYLIMIDAZO[4,5-F] QUINOLINE (IQ) - DNA-BINDING IN RATS GIVEN CHLOROPHYLLIN - DOSE-RESPONSE AND TIME-COURSE STUDIES IN THE LIVER AND COLON [J].
GUO, D ;
DASHWOOD, R .
CARCINOGENESIS, 1994, 15 (04) :763-766
[9]   SUPPRESSION OF DIETHYLNITROSAMINE-INITIATED PRENEOPLASTIC FOCI DEVELOPMENT IN THE RAT-LIVER BY COMBINED ADMINISTRATION OF 4 ANTIOXIDANTS AT LOW-DOSES [J].
HASEGAWA, R ;
TIWAWECH, D ;
HIROSE, M ;
TAKABA, K ;
HOSHIYA, T ;
SHIRAI, T ;
ITO, N .
JAPANESE JOURNAL OF CANCER RESEARCH, 1992, 83 (05) :431-437
[10]  
Higgins GM, 1931, ARCH PATHOL, V12, P186