| Literature DB >> 8609060 |
T Kato1, R Hasegawa, D Nakae, M Hirose, M Yaono, L Cui, Y Kobayashi, Y Konishi, N Ito, T Shirai.
Abstract
Male F344 rats were administered 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) in the diet at doses of 200, 50, 12.5, 3.2, 0.8, 0.2 and 0.05 ppm for six weeks, and partially hepatectomized 1 week after the beginning of MeIQx administration. Quantitative values for glutathione S-transferase placental form (GST-P)-positive foci in the liver were dose-dependently increased by the MeIQx treatment. 8-Hydroxyguanine (8-OHG) levels assessed after 1 week of dietary MeIQx administration were also dose-dependently increased, although the effect was no longer observed at the end of the treatment period. The correlation between numbers of GST-P-positive foci at week 6 and 8-OHG levels at week 1 was linear, values for both parameters being higher than the control levels even in the 0.8 ppm dose group. These findings indicate that, in addition to the previously reported MeIQx-DNA adduct formation, DNA modifications due to oxidative damage may play an important role in MeIQx liver carcinogenesis in rats.Entities:
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Year: 1996 PMID: 8609060 PMCID: PMC5921060 DOI: 10.1111/j.1349-7006.1996.tb03149.x
Source DB: PubMed Journal: Jpn J Cancer Res ISSN: 0910-5050