In vivo genotoxicity of heterocyclic amines detected by a modified alkaline single cell gel electrophoresis assay in a multiple organ study in the mouse

被引:38
作者
Sasaki, YF
Saga, A
Akasaka, M
Nishidate, E
Watanabe-Akanuma, M
Ohta, T
Matsusaka, N
Tsuda, S
机构
[1] Hachinohe Inst Technol, Fac Chem & Biol Engn, Lab Genotox, Hachinohe, Aomori 03911, Japan
[2] Inst Environm Toxicol, Tokyo 187, Japan
[3] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Tokyo 19203, Japan
[4] Iwate Univ, Fac Agr, Dept Vet Med, Lab Vet Publ Hlth, Morioka, Iwate 020, Japan
关键词
heterocyclic amine; Trp-P-1; Trp-P-2; IQ; MeIQ; MeIQx; PhIP; genotoxicity; mouse multiple organs; alkaline single cell gel electrophoresis (SCG) assay;
D O I
10.1016/S1383-5718(97)00142-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We used a modification of the alkaline single cell gel electrophoresis (SCG) (Comet) assay to test the in vivo genotoxicity of 6 heterocyclic amines, Trp-P-1 (25 mg/kg), Trp-P-2 (13 mg/kg), IQ (13 mg/kg), MeIQ (13 mg/kg), MeIQx (13 mg/kg) and PhIP (40 mg/kg), in mouse liver, lung, kidney, brain, spleen, bone marrow and stomach mucosa, Mice were sacrificed 1, 3, and 24 h after intraperitoneal injection. Trp-P-2, IQ, MeIQ, and MeIQx yielded statistically significant DNA damage in the stomach, liver; kidney, lung and brain; Trp-P-1 in the stomach, liver and lung; and PhIP in the liver, kidney and brain. None of the heterocyclic amines induced DNA damage in the spleen and bone marrow. Our results suggest that the alkaline SCG assay applied to multiple organs is a good way to detect organ-specific genotoxicity of heterocyclic amines in mammals. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:57 / 73
页数:17
相关论文
共 39 条
[1]   CARCINOGENICITY OF 2-AMINO-3-METHYLIMIDAZO[4,5-F]QUINOLINE IN NONHUMAN-PRIMATES - INDUCTION OF TUMORS IN 3 MACAQUES [J].
ADAMSON, RH ;
THORGEIRSSON, UP ;
SNYDERWINE, EG ;
THORGEIRSSON, SS ;
REEVES, J ;
DALGARD, DW ;
TAKAYAMA, S ;
SUGIMURA, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 1990, 81 (01) :10-14
[2]   EFFECT OF HETEROCYCLIC AMINES AND BEEF EXTRACT ON CHROMOSOME-ABERRATIONS AND SISTER CHROMATID EXCHANGES IN CULTURED HUMAN-LYMPHOCYTES [J].
AESCHBACHER, HU ;
RUCH, E .
CARCINOGENESIS, 1989, 10 (03) :429-433
[3]  
ALEXANDER J, 1989, VAR FODA S2, V42, P9
[4]  
AUNE T, 1988, CARCINOGENESIS, V7, P2723
[5]   APOPTOSIS - MOLECULAR CONTROL POINT IN TOXICITY [J].
CORCORAN, GB ;
FIX, L ;
JONES, DP ;
MOSLEN, MT ;
NICOTERA, P ;
OBERHAMMER, FA ;
BUTTYAN, R .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 128 (02) :169-181
[6]   MUTAGENIC ACTIVATION OF 3-AMINO-1,4-DIMETHYL-5H-PYRIDO(4,3-B)INDOLE(TRP-P-1) AND 3-AMINO-1-METHYL-5H-PYRIDO(4,3-B)INDOLE (TRP-P-2) BY PRIMARY CULTURES OF ADULT-RAT HEPATOCYTES - EFFECT OF AROCLOR INDUCTION INVITRO [J].
DECLOITRE, F ;
HAMON, G ;
MARTIN, M ;
THYBAUDLAMBAY, V .
MUTATION RESEARCH, 1984, 137 (2-3) :123-132
[7]   INDUCTION OF LYMPHOMA IN CDF1 MICE BY THE FOOD MUTAGEN, 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE [J].
ESUMI, H ;
OHGAKI, H ;
KOHZEN, E ;
TAKAYAMA, S ;
SUGIMURA, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 1989, 80 (12) :1176-1178
[8]   THE COMET ASSAY - A COMPREHENSIVE REVIEW [J].
FAIRBAIRN, DW ;
OLIVE, PL ;
ONEILL, KL .
MUTATION RESEARCH-REVIEWS IN GENETIC TOXICOLOGY, 1995, 339 (01) :37-59
[9]   IDENTIFICATION OF THE MUTAGENS IN COOKED BEEF [J].
FELTON, JS ;
KNIZE, MG ;
SHEN, NH ;
ANDRESEN, BD ;
BJELDANES, LF ;
HATCH, FT .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1986, 67 :17-24
[10]   INNOVATIVE DESIGNS AND PRACTICES FOR ACUTE SYSTEMIC TOXICITY STUDIES [J].
GAD, SC ;
SMITH, AC ;
CRAMP, AL ;
GAVIGAN, FA ;
DERELANKO, MJ .
DRUG AND CHEMICAL TOXICOLOGY, 1984, 7 (05) :423-434