Lu S X, Montesano R, Bresil H, Lu L Y, Xiao G L
Zhonghua Zhong Liu Za Zhi. 1987 Jan;9(1):21-4.
Effect of molybdenum on the alkylation of DNA in the liver of rats treated with 14C-diethylnitrosamine was studied. When administered orally at a dose of 1 mg/rat/day as (HN4)6 Mo7O24 for 30 days, Mo inhibited the alkylation of DNA in the liver of rats. The level of 3-ethylguanine, N7-ethylguanine and O6-ethylguanine decreased. Simultaneously, the exhalation of 14CO2 and the urinary excretion of 14C- were increased as compared to the controls. At a dose of 5 mg/rat/day, Mo increased the alkylation of DNA in the liver. The amount of 3-ethylguanine, N7-ethylguanine and O6-ethylguanine was higher than that of the controls. The exhalation of 14CO2 and the urinary excretion of 14C- were decreased. The authors believe that the dose of molybdenum is relevant to the role it plays in the carcinogenesis of cell. The role of molybdenum in the carcinogenesis is discussed.
研究了钼对用14C-二乙基亚硝胺处理的大鼠肝脏中DNA烷基化的影响。当以(NH4)6Mo7O24的形式按1毫克/大鼠/天的剂量口服给药30天时,钼抑制了大鼠肝脏中DNA的烷基化。3-乙基鸟嘌呤、N7-乙基鸟嘌呤和O6-乙基鸟嘌呤的水平降低。同时,与对照组相比,14CO2的呼出量和14C-的尿排泄量增加。当剂量为5毫克/大鼠/天时,钼增加了肝脏中DNA的烷基化。3-乙基鸟嘌呤、N7-乙基鸟嘌呤和O6-乙基鸟嘌呤的量高于对照组。14CO2的呼出量和14C-的尿排泄量减少。作者认为钼的剂量与其在细胞致癌作用中所起的作用有关。讨论了钼在致癌作用中的作用。