Furihata C, Hatta A, Sato Y, Matsushima T
Department of Molecular Oncology, University of Tokyo, Japan.
Mutat Res. 1989 Aug;213(2):227-31. doi: 10.1016/0027-5107(89)90154-1.
DNA damage in the pyloric mucosa of the stomach of male F344 rats was determined by the alkaline elution method after administration of glyoxal, a direct-acting mutagen present in various heated foods, by gastric intubation. Glyoxal at doses of 50-550 mg/kg body weight induced DNA damage in the pyloric mucosa of rat stomach, detected by a 5- to 12-fold increase in the elution rate constant 2 h after its administration. N-Methyl-N'-nitro-N-nitrosoguanidine, a glandular stomach carcinogen, used as a positive control at doses of 1-100 mg/kg body weight induced a 11- to 24-fold increase in the elution rate constant, while 2-acetylaminofluorene, which is not a gastric carcinogen, given as a negative control at doses of 200-400 mg/kg body weight did not increase the elution rate constant. Thus glyoxal, which was previously suggested to induce unscheduled DNA synthesis in the pyloric mucosa of rat stomach, was confirmed to be genotoxic in this region.
通过胃插管给雄性F344大鼠施用乙二醛(一种存在于各种加热食物中的直接作用诱变剂)后,采用碱性洗脱法测定大鼠胃幽门黏膜中的DNA损伤。体重剂量为50 - 550 mg/kg的乙二醛可诱导大鼠胃幽门黏膜的DNA损伤,给药2小时后洗脱速率常数增加5至12倍可检测到该损伤。体重剂量为1 - 100 mg/kg的腺胃致癌物N-甲基-N'-硝基-N-亚硝基胍用作阳性对照,可使洗脱速率常数增加11至24倍,而体重剂量为200 - 400 mg/kg的非胃致癌物2-乙酰氨基芴作为阴性对照,并未增加洗脱速率常数。因此,先前曾提示可诱导大鼠胃幽门黏膜非定标性DNA合成的乙二醛,在此区域被确认为具有遗传毒性。