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Mutagenesis vol. 12 no. 3 pp. 179-184, 1997
© 1997 UK Environmental Mutagen Society/Oxford University Press


research-article

Sodium phenobarbital–enhanced mutation frequency in the liver DNM of lacz transgenic mice treated with diethylnitrosamine

Naoko Okada, Ayako Honda, Masayoshi Kawabata and Nobuhiro Yajima1

Research Institute of Life Science Snow Brand Milk Products Co, Ltd, 519 Shimo–Ishibashi, Ishibashi–Machi, Shimotsuga–gun, Tochigi 329–05, Japan

To investigate how a carcinogenic promoter acts on cells mutated by an initiator, we used as a model, lacZ transgenic mouse and a positive selection system. Preliminary data for the mutational events in liver DNA of the mice was generated using diethylnitrosamine (DEN) and sodium phenobarbital (S-PB) as initiator and promoter, respectively. In our first experiment, male MutaTMice received a single i.p. injection of saline or 100 mg/kg DEN and were fed a normal diet for 7 days and 500 p.p.m. S-PB in the diet for 21 days. Liver DNA was harvested after a 1 night fast on days 7 and 28 post-DEN treatment. In our second experiment, male mice received a single i.p. injection of phosphate buffered saline or 50 mg/kg DEN and were fed a normal diet for 7 days, a diet with S-PB for 14 days and then a normal diet for 7 days. Liver DNA was harvested after a 1 night fast on days 7, 21 and 28 post-DEN treatment. The S-PB diet enhancedabsolute and relative liver weights in all groups. The single intraperitoneal dose of 50 or 100 mg/kg DEN induced high mutation frequencies (MF) in liver, lacZ genes on days 7, 21 and 28. There were no remarkable differences of the MF among any sampling days for animals receiving DEN and a normal diet. S-PB feeding at 500 p.p.m. for 21 days failed to affect the MF in groups given saline or 100 mg/kg DEN. On the other hand, when 50 mg/kg DEN was given, S-PB feeding at 500 p.p.m. for 14 days elevated the MF in liver DNA on days 21 and 28 to –1.8 and 4.0 times the MF, respectively,of the mice fed the normal diet. Consequently, S-PB might preferentially promote certain initiated cells participating in a balance between cell death and proliferation.

1To whom correspondence should be addressed


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CarcinogenesisHome page
F. Tombolan, D. Renault, D. Brault, M. Guffroy, F. Perin, and V. Thybaud
Effect of mitogenic or regenerative cell proliferation on lacz mutant frequency in the liver of MutaTMMice treated with 5,9-dimethyldibenzo[c,g]carbazole
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[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
F. Tombolan, D. Renault, D. Brault, M. Guffroy, O. Perin-Roussel, F. Perin, and V. Thybaud
Kinetics of induction of DNA adducts, cell proliferation and gene mutations in the liver of Muta(TM)Mice treated with 5,9-dimethyldibenzo[c,g]carbazole
Carcinogenesis, January 1, 1999; 20(1): 125 - 132.
[Abstract] [Full Text] [PDF]



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