Bull R J, Robinson M, Stober J A
Cancer Lett. 1984 Sep;24(2):209-12. doi: 10.1016/0304-3835(84)90138-1.
Doses of acrylamide ranging from 12.5 to 50 mg/kg were administered orally to female ICR-Swiss mice over 3 days for each of 2 weeks (total doses of 75, 150 and 300 mg/kg). Two weeks later some of the animals were started on a promotion schedule involving the application of 2.5 micrograms TPA/mouse 3 times weekly. Development of tumors was observed weekly in the skin, and in the lungs at 1 year. Acrylamide was found to initiate squamous cell adenoma and carcinomas in the skin and increased the yield of adenomas and carcinomas in the lung. Skin tumor development was dependent upon 12-O-tetradecanoylphorbol-13-acetate (TPA) promotion whereas lung tumor induction was not. These data extend previous observations of carcinogenic activity of acrylamide in the skin of SENCAR mice and lungs of strain A/J mice to a third strain of mouse, the ICR-Swiss.
将剂量为12.5至50毫克/千克的丙烯酰胺经口给予雌性ICR - 瑞士小鼠,为期3天,共2周(总剂量分别为75、150和300毫克/千克)。两周后,部分动物开始接受促癌方案,即每周3次,每次给每只小鼠涂抹2.5微克佛波酯(TPA)。每周观察皮肤肿瘤的发生情况,1年后观察肺部肿瘤的发生情况。结果发现,丙烯酰胺可引发皮肤鳞状细胞腺瘤和癌,并增加肺部腺瘤和癌的发生率。皮肤肿瘤的发生依赖于12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)的促癌作用,而肺部肿瘤的诱发则不依赖于此。这些数据将先前关于丙烯酰胺在SENCAR小鼠皮肤和A/J品系小鼠肺部致癌活性的观察结果扩展到了第三种小鼠品系——ICR - 瑞士小鼠。