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
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.