Kato T, Hasegawa R, Nakae D, Hirose M, Yaono M, Cui L, Kobayashi Y, Konishi Y, Ito N, Shirai T
First Department of Pathology, Nagoya City University Medical School, Japan.
Jpn J Cancer Res. 1996 Feb;87(2):127-33. doi: 10.1111/j.1349-7006.1996.tb03149.x.
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.
将雄性F344大鼠的饲料中分别添加剂量为200、50、12.5、3.2、0.8、0.2和0.05 ppm的2-氨基-3,8-二甲基咪唑并[4,5-f]喹喔啉(MeIQx),持续六周,并在开始给予MeIQx一周后进行部分肝切除。MeIQx处理后,肝脏中谷胱甘肽S-转移酶胎盘型(GST-P)阳性灶的定量值呈剂量依赖性增加。给予MeIQx饮食一周后评估的8-羟基鸟嘌呤(8-OHG)水平也呈剂量依赖性增加,尽管在治疗期结束时不再观察到这种效应。第6周时GST-P阳性灶数量与第1周时8-OHG水平之间的相关性呈线性,即使在0.8 ppm剂量组中,这两个参数的值也高于对照水平。这些发现表明,除了先前报道的MeIQx-DNA加合物形成外,氧化损伤引起的DNA修饰可能在大鼠MeIQx诱导的肝脏致癌作用中起重要作用。