Lijinsky W, Reuber M D
Carcinogenesis. 1980 Jun;1(6):501-3. doi: 10.1093/carcin/1.6.501.
The cis and trans isomers of nitroso-2,6-dimethylmorpholine (Me2NMOR) have been separated and administered to Fischer 344 rats at doses corresponding to their proportion in the mixture prepared from the commercial amine (approximately 2 cis to 1 trans). The mixture of isomers was given at 2 doses, 50 mg per liter of drinking water and 20 mg per liter. A standard volume of each solution was given (20 ml per day per rat) on 5 days of each week and the animals were treated for the same time at either higher or lower dose levels. Almost all of the animals died with basal cell carcinomas and/or papillomas of the upper gastrointestinal tract. The time at which the rats died with the tumors was used as a measure of carcinogenic potency. Survival of the treated animals was consistently longer at the lower dose of each isomer. It was concluded that the trans isomer of Me2NMOR is a more potent carcinogen in rats than the cis isomer.
亚硝基 - 2,6 - 二甲基吗啉(Me2NMOR)的顺式和反式异构体已被分离,并以与从市售胺制备的混合物中它们的比例相对应的剂量给予Fischer 344大鼠(大约2个顺式对1个反式)。异构体混合物以两种剂量给予,每升饮用水50毫克和每升20毫克。每周5天给予每种溶液标准体积(每只大鼠每天20毫升),并且动物在较高或较低剂量水平下接受相同时间的治疗。几乎所有动物都死于上消化道的基底细胞癌和/或乳头状瘤。大鼠死于肿瘤的时间用作致癌效力的衡量标准。在每种异构体的较低剂量下,经治疗动物的存活时间始终更长。得出的结论是,Me2NMOR的反式异构体在大鼠中比顺式异构体是更有效的致癌物。