Literature DB >> 8106289

Long-Evans A and C rat strains susceptible to clastogenic effects of chemicals in the bone marrow cells.

Y Ito1, K Fujie, S Matsuda, R Takahashi, S Maeda.   

Abstract

The clastogenic responses to direct- and indirect-acting carcinogens in bone marrow cells of LEA, LEC, Wistar and SD rats were compared. The frequency of chromosome aberrations (CA) induced by n-butyl-N-nitrosourea or methylmethanesulfonate (MMS), which does not need metabolic activation, was significantly higher in both LEA and LEC rats than in Wistar or SD rats. When bone marrow cells of each rat strain were exposed to MMS in vitro, they also showed the same tendency in CA frequency. Therefore, the high sensitivity of both LEA and LEC rats to the clastogenic effects of direct-acting carcinogens seems to result from the sensitivity of the bone marrow cells themselves. On the other hand, the CA frequency induced by 7,12-dimethylbenz[a]anthracene (DMBA) or aflatoxin B1 (AFB1), which requires metabolic activation, was lower in LEC rats than in the other 3 strains. The CA frequency induced by DMBA or AFB1 in LEC rats fed Cu-free diet since birth (Cu-free LEC rats) was higher than that in LEC rats given normal diet and lower than that in LEA rats, although the difference was statistically significant only between Cu-free LEC rats and LEC rats treated with DMBA. The copper concentrations in the livers of LEA, Cu-free LEC and LEC male rats aged 4 weeks were 5.0 +/- 0.4, 33 +/- 7.7 and 106 +/- 3.4 micrograms/g wet weight, respectively. These results suggest that the lower sensitivity of LEC rats to the clastogenic effects of indirect-acting carcinogens may be due to the effect of the large amount of copper accumulated in LEC rat liver.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8106289      PMCID: PMC5919336          DOI: 10.1111/j.1349-7006.1994.tb02882.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


Long‐Evans rat LE rat with a cinnamon‐like coat color LE rat with an agouti coat color LEC rat fed Cu‐free diet since birth chromosome aberrations 7,12‐dimethyl‐benz [a] anthracene 7,8,12‐trimethylbenz[a]anthracene aflatoxin B1 n‐butyl‐N‐nitrosourea methylmethanesulfonate
  14 in total

1.  Specific vulnerability of the largest telocentric chromosome of rat bone marrow cells to 7,12-dimethylbenz[a]anthracene.

Authors:  T Sugiyama
Journal:  J Natl Cancer Inst       Date:  1971-12       Impact factor: 13.506

2.  Acute cytogenetic effect of sterigmatocystin on rat bone-marrow cells in vivo.

Authors:  N Ueda; K Fujie; K Gotoh-Mimura; S C Chattopadhyay; T Sugiyama
Journal:  Mutat Res       Date:  1984-04       Impact factor: 2.433

3.  Studies on the induction of DAB metabolizing enzyme activity and other microsomal enzyme activity in the liver of rats fed copper.

Authors:  Y Yamane; K Sakai
Journal:  Chem Pharm Bull (Tokyo)       Date:  1975-07       Impact factor: 1.645

4.  Cytochrome P-450 and chromosome damage by cyclophosphamide in LEC strain rats predisposed to hereditary hepatitis and liver cancer.

Authors:  R Masuda; S Abe; M C Yoshida; M Sasaki; T Sugiyama; N Taniguchi
Journal:  Mutat Res       Date:  1990-08       Impact factor: 2.433

5.  Acute cytogenetic effect of 2-(2-furyl)-3-(5-nitro-2-furyl)-acrylamide (AF-2, a food preservative) on rat bone marrow cells in vivo.

Authors:  T Sugiyama; K Goto; H Uenaka
Journal:  Mutat Res       Date:  1975-08       Impact factor: 2.433

6.  Effect of basic cupric acetate on biochemical changes in the liver of the rat fed carcinogenic aminoazo dye. III. Effect of copper compared with some other metals, phenobarbital and 3-methylcholanthrene on the metabolism of 4-dimethylaminoazobenzene.

Authors:  Y Yamane; K Sakai
Journal:  Chem Pharm Bull (Tokyo)       Date:  1974-05       Impact factor: 1.645

7.  New mutation causing hereditary hepatitis in the laboratory rat.

Authors:  M C Yoshida; R Masuda; M Sasaki; N Takeichi; H Kobayashi; K Dempo; M Mori
Journal:  J Hered       Date:  1987 Nov-Dec       Impact factor: 2.645

8.  Suppression of 7,12-dimethylbenz[a]anthracene-induced chromosome aberrations in rat bone marrow cells after treatment with Sudan III and related azo dyes.

Authors:  Y Ito; S Maeda; T Fujihara; N Ueda; T Sugiyama
Journal:  J Natl Cancer Inst       Date:  1982-12       Impact factor: 13.506

9.  Cytogenetic studies of leukemia induced by 6,8,12-and 7,8,12-trimethylbenz(a)anthracene.

Authors:  T Sugiyama; F P Brillantes
Journal:  J Exp Med       Date:  1970-02       Impact factor: 14.307

10.  Abnormal copper accumulation in non-cancerous and cancerous liver tissues of LEC rats developing hereditary hepatitis and spontaneous hepatoma.

Authors:  Y Li; Y Togashi; S Sato; T Emoto; J H Kang; N Takeichi; H Kobayashi; Y Kojima; Y Une; J Uchino
Journal:  Jpn J Cancer Res       Date:  1991-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.