SYNERGISTIC ENHANCEMENT OF HEPATIC FOCI DEVELOPMENT BY COMBINED TREATMENT OF RATS WITH 10 HETEROCYCLIC AMINES AT LOW-DOSES

Citation
R. Hasegawa et al., SYNERGISTIC ENHANCEMENT OF HEPATIC FOCI DEVELOPMENT BY COMBINED TREATMENT OF RATS WITH 10 HETEROCYCLIC AMINES AT LOW-DOSES, Carcinogenesis, 15(5), 1994, pp. 1037-1041
Citations number
26
Categorie Soggetti
Oncology
Journal title
ISSN journal
01433334
Volume
15
Issue
5
Year of publication
1994
Pages
1037 - 1041
Database
ISI
SICI code
0143-3334(1994)15:5<1037:SEOHFD>2.0.ZU;2-O
Abstract
Potential synergism between 10 carcinogenic heterocyclic amines [3-ami no-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1), 3-amino-1-methyl-5H- pyrido[4,3-b]indole (Trp-P-2), 2-amino-6 methyldipyrido[1,2-a:3',2'-d] imidazole (Glu-P-1), 2-amino-dipyrido[1,2-a:3',2'-d]imidazole (Glu-P-2 ), 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-amino-3,4-dimethyli midazo[4,5-f]quinoline (MeIQ), 2-amino-3,8-dimethylimidazo[4,5-f]quino xaline (MeIQx), 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeA alpha C), 2-amino-9H-pyrido[2,3-b]indole (A alpha C) and 2-amino-1-methyl-6-phe nylimidazo[4,5-b]pyridine (PhIP)] in rat liver carcinogenesis was exam ined. Male F344 rats were initially given diethylnitrosamine (200 mg/k g, i.p.) and beginning 2 weeks later received heterocyclic amines indi vidually at doses 1/10 of that proven to be carcinogenic or in combina tion at 1/10 or 1/100 doses for 6 weeks. All animals were subjected to partial hepatectomy at week 3 and killed at week 8. The induction of immunohistochemically demonstrable placental glutathione S-transferase positive foci was significantly increased in rats given all 10 chemic als in combination at the 1/10 dose level while values were almost the same as in controls with the 1/100 dose mixture and the individual ch emicals, except for Glu-P-1 which significantly increased foci develop ment and Glu-P-2 and A alpha c which significantly decreased levels of foci at the 1/10 dose level. Thus apparent synergism was observed wit h the 1/10 dose level combination. When the data are considered togeth er with our previous results obtained with five heterocyclic amines us ing 1/1, 1/5 and 1/25 dose levels, combined effects were found to be r elated to the number of chemicals included and the dose levels of each , with a possible isoadditive influence being common. The findings are of particular significance since heterocyclic amines and other carcin ogenic agents might be simultaneously generated during cooking.