Althoff J, Mohr U, Lijinsky W
J Cancer Res Clin Oncol. 1985;109(3):183-7. doi: 10.1007/BF00390354.
The effect of N-nitroso-2,6-dimethylmorpholine (NDMM), a pancreatic carcinogen for the Syrian golden hamster, was examined in the European hamster (EH) for comparative reasons. The compound was administered by subcutaneous (SC) injection or intragastric gavage (IG) at a dose level corresponding to 0.1 of LD50. In terms of carcinogenicity the main target was the respiratory epithelium (nasal cavity, lung, trachea, larynx); other benign and malignant tumors originated in the liver (bile duct epithelium and endothelium) and renal pelvis (transitional epithelium). The occurrence of neoplasms seen at other sites was difficult to attribute to treatment. Reduced metabolism as found during hibernation did not change the organ distribution of neoplastic growths. Differences in the carcinogenic potency (tumor incidence and latency, affected organs and cell types) did not depend significantly on the route of administration. The data were compared to those obtained using other nitroso compounds in this species.
出于比较的目的,在欧洲仓鼠(EH)中研究了N-亚硝基-2,6-二甲基吗啉(NDMM)对叙利亚金仓鼠的胰腺致癌作用。该化合物通过皮下(SC)注射或灌胃(IG)给药,剂量水平相当于LD50的0.1。就致癌性而言,主要靶器官是呼吸道上皮(鼻腔、肺、气管、喉);其他良性和恶性肿瘤起源于肝脏(胆管上皮和内皮)和肾盂(移行上皮)。在其他部位出现的肿瘤很难归因于治疗。冬眠期间发现的代谢降低并没有改变肿瘤生长的器官分布。致癌效力(肿瘤发生率和潜伏期、受影响的器官和细胞类型)的差异并不显著取决于给药途径。将这些数据与使用该物种的其他亚硝基化合物获得的数据进行了比较。