Lijinsky W, Taylor H W
Int J Cancer. 1975 Aug 15;16(2):318-22. doi: 10.1002/ijc.2910160215.
The carcinogenicity of nitrosopiperidine and five methylated derivatives was compared by feeding them to rats at equimolar concentrations in drinking water, at the rate of 20 ml per day, 5 days a week. The maximum treatment time was 50 weeks. Nitrosopiperidine, 2-methyl-, 3-methyl- and 4-methyl-nitrosopiperidine induced tumors of the nasal turbinates or upper gastrointestinal tract in almost 100% of the animals. There was a significantly longer time to death from these tumors in the group treated with 2-methylnitrosopiperidine and a number of hepatocellular carcinomas appeared in this longer lived group. Very few tumors of these sites were seen in rats treated with 2,6-dimethyl- or 2,2,6,6-tetramethyl-nitrosopiperidine. It was concluded that blockage by methyl groups of one or more carbon atoms alpha to the nitroso function in nitrosopiperidine significantly reduces carcinogenic activity of the molecule.
通过以等摩尔浓度将亚硝基哌啶及其五种甲基化衍生物添加到大鼠饮用水中,每天20毫升,每周5天的方式,比较它们的致癌性。最长治疗时间为50周。亚硝基哌啶、2-甲基-、3-甲基-和4-甲基亚硝基哌啶在几乎100%的动物中诱发鼻甲或上消化道肿瘤。在接受2-甲基亚硝基哌啶治疗的组中,死于这些肿瘤的时间明显更长,并且在这个存活时间更长的组中出现了一些肝细胞癌。在用2,6-二甲基-或2,2,6,6-四甲基亚硝基哌啶治疗的大鼠中,很少见到这些部位的肿瘤。得出的结论是,亚硝基哌啶中亚硝基官能团α位的一个或多个碳原子被甲基阻断会显著降低该分子的致癌活性。