Anderson L M, Carter J P, Driver C L, Logsdon D L, Kovatch R M, Giner-Sorolla A
Laboratory of Comparative Carcinogenesis, National Cancer Institute, Frederick, MD.
Cancer Lett. 1993 Jan 15;68(1):61-6. doi: 10.1016/0304-3835(93)90220-4.
Inclusion of 10% ethanol with 6.8 ppm N-nitrosodiethylamine in the drinking water of strain A male mice resulted in a 4-fold enhancement of multiplicity of lung tumors and a 16-fold increase in incidence of fore-stomach tumors, compared with carcinogen alone. Given with 40 ppm N-nitrosopyrrolidine, ethanol caused a 5.5-fold increase in lung tumor multiplicity. The inclusion of 15% ethanol with N6-(methylnitroso)adenosine, given orally to Swiss female mice, led to reduced body weights and shortened survival time related to hemangiosarcoma occurrence or increased incidence of thymic lymphoma, depending on dose of carcinogen. The data provide additional support for the proposal that co-administered ethanol increases the tumorigenicity of nitrosamines by blocking hepatic first-pass clearance.
在A品系雄性小鼠的饮用水中加入含6.8 ppm N-亚硝基二乙胺的10%乙醇,与单独使用致癌物相比,肺部肿瘤的多样性增加了4倍,前胃肿瘤的发生率增加了16倍。与40 ppm N-亚硝基吡咯烷一起使用时,乙醇使肺部肿瘤的多样性增加了5.5倍。给瑞士雌性小鼠口服含N6-(甲基亚硝基)腺苷的15%乙醇,根据致癌物的剂量,会导致体重减轻和生存时间缩短,这与血管肉瘤的发生或胸腺淋巴瘤的发生率增加有关。这些数据为共同给予乙醇通过阻断肝脏首过清除增加亚硝胺的致癌性这一观点提供了更多支持。