Althoff J, Grandjean C, Gold B
J Natl Cancer Inst. 1978 Jan;60(1):197-9. doi: 10.1093/jnci/60.1.197.
N-Nitroso-2,6-dimethylmorpholine (DMNM) was examined in Syrian golden hamsters in a comparative study of N-N-dipropylnitrosamine (DPN) metabolites. DMNM was administered sc, and the results were compared with those of a previous study in which the compound was given intragastrically. DMNM was more toxic when administered sc, and the respiratory tract was the main target organ (with a 100% tumor incidence). With an sc administration, neoplasms occurred earlier in the hamsters than with an intragastric administration, and fewer tumors of the pancreas and biliary tract were found. However, neoplasms of the upper digestive tract and vagina were seen only with sc treatment. These studies indicated the importance of the treatment route but did not substantiate the role of common metabolites, such as DMNM, formed by beta-oxidation from DPN, with regard to induction of a given tumor type.
在一项关于N-亚硝基二丙胺(DPN)代谢产物的比较研究中,对叙利亚金黄地鼠进行了N-亚硝基-2,6-二甲基吗啉(DMNM)的研究。DMNM通过皮下注射给药,并将结果与之前该化合物经胃内给药的研究结果进行比较。皮下注射DMNM时毒性更大,呼吸道是主要靶器官(肿瘤发生率为100%)。与胃内给药相比,皮下注射时仓鼠体内肿瘤出现得更早,且胰腺和胆道肿瘤较少。然而,仅在皮下注射治疗时观察到上消化道和阴道肿瘤。这些研究表明了给药途径的重要性,但并未证实由DPN经β-氧化形成的常见代谢产物(如DMNM)在诱导特定肿瘤类型方面的作用。