Lijinsky W, Taylor H W
Cancer Res. 1976 Jun;36(6):1988-90.
N-Nitrosopyrrolidine and two of its derivatives were prepared and fed in drinking water to Sprague-Dawley rats to compare the effects of substituents on the carcinogenicity of the N-nitrosopyrrolidine molecule. 3,4-Dichloro-N-nitrosopyrrolidine induced esophageal tumors in 13 of 14 animals, olfactory carcinomas in 4, and a hepatocellular tumor in 1. All animals that received this compound were dead at 55 weeks after the start of the experiments. N-Nitrosopyrrolidine induced hepatocellular tumors in 26 of 29 animals and induced 1 olfactory carcinoma. Not all animals in this group were dead until 104 weeks of the experiment. 2,5-Dimethyl-N-nitrosopyrrolidine induced only 2 hepatocellular tumors in 29 animals. The alpha-methyl substitution diminished the liver carcinogenicity, while the beta chlorine substitution affected a different target organ, the esophagus, and greatly reduced the time to death with tumors.
制备了N-亚硝基吡咯烷及其两种衍生物,并将其添加到饮用水中喂给斯普拉格-道利大鼠,以比较取代基对N-亚硝基吡咯烷分子致癌性的影响。3,4-二氯-N-亚硝基吡咯烷在14只动物中的13只诱发了食管肿瘤,4只诱发了嗅癌,1只诱发了肝细胞肿瘤。所有接受该化合物的动物在实验开始后55周死亡。N-亚硝基吡咯烷在29只动物中的26只诱发了肝细胞肿瘤,并诱发了1例嗅癌。该组并非所有动物在实验104周时都死亡。2,5-二甲基-N-亚硝基吡咯烷在29只动物中仅诱发了2例肝细胞肿瘤。α-甲基取代降低了肝脏致癌性,而β-氯取代影响了不同的靶器官——食管,并大大缩短了肿瘤导致的死亡时间。