Literature DB >> 8200065

Synergistic enhancement of hepatic foci development by combined treatment of rats with 10 heterocyclic amines at low doses.

R Hasegawa1, E Miyata, M Futakuchi, A Hagiwara, M Nagao, T Sugimura, N Ito.   

Abstract

Potential synergism between 10 carcinogenic heterocyclic amines [3-amino-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-dimethyl-imidazo[4,5-f]quinoline (MeIQ), 2-amino-3,8-dimethyl-imidazo[4,5-f]quinoxaline (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-phenylimidazo[4,5-b]pyridine (PhIP)] in rat liver carcinogenesis was examined. Male F344 rats were initially given diethylnitrosamine (200 mg/kg, i.p.) and beginning 2 weeks later received heterocyclic amines individually at doses 1/10 of that proven to be carcinogenic or in combination 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 chemicals 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 chemicals, except for Glu-P-1 which significantly increased foci development 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 with the 1/10 dose level combination. When the data are considered together with our previous results obtained with five heterocyclic amines using 1/1, 1/5 and 1/25 dose levels, combined effects were found to be related 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 carcinogenic agents might be simultaneously generated during cooking.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8200065     DOI: 10.1093/carcin/15.5.1037

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  4 in total

1.  Medium-term bioassays for carcinogenicity of chemical mixtures.

Authors:  N Ito; K Imaida; M Hirose; T Shirai
Journal:  Environ Health Perspect       Date:  1998-12       Impact factor: 9.031

Review 2.  Toxicology of chemical mixtures: international perspective.

Authors:  V J Feron; F R Cassee; J P Groten
Journal:  Environ Health Perspect       Date:  1998-12       Impact factor: 9.031

3.  Analysis of synergism in hepatocarcinogenesis based on preneoplastic foci induction by 10 heterocyclic amines in the rat.

Authors:  R Hasegawa; I Yoshimura; K Imaida; N Ito; T Shirai
Journal:  Jpn J Cancer Res       Date:  1996-11

4.  Hepatocyte growth factor enhancement of preneoplastic hepatic foci development in rats treated with diethylnitrosamine and N-ethyl-N-hydroxyethylnitrosamine.

Authors:  M Yaono; R Hasegawa; Y Mizoguchi; M Futakuchi; T Nakamura; N Ito; T Shirai
Journal:  Jpn J Cancer Res       Date:  1995-08
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.