Brusick D, Jagannath D, Weekes U
Mutat Res. 1976 Nov 1;41(1 spel. no):51-60. doi: 10.1016/0027-5107(76)90073-7.
The carcinogen dimethylnitrosamine (DMNA) is known to exhibit a high degree of strain, organ, age, and sex related tumor specificity in mice. Using microbial mutagenesis assay coupled with mouse tissue microsomal enzyme activation systems, evidence has been obtained that demonstrated a close relationship between the level of in vitro DMNA activation to a mutagen and in vivo tumor susceptibility. DMNA activation by liver, lung, and kidney microsomes from several mouse strains was compared by measuring the rate of mutagenic metabolites formed during incubation of the carcinogen in mutation assays using Salmonella typhimurium G-46 as the indicator microorganism.
已知致癌物二甲基亚硝胺(DMNA)在小鼠中表现出高度的品系、器官、年龄和性别相关的肿瘤特异性。通过微生物诱变试验结合小鼠组织微粒体酶激活系统,已获得证据表明体外DMNA活化为诱变剂的水平与体内肿瘤易感性之间存在密切关系。以鼠伤寒沙门氏菌G-46作为指示微生物,通过测量致癌物在突变试验中孵育期间形成诱变代谢物的速率,比较了几种小鼠品系的肝脏、肺和肾脏微粒体对DMNA的激活情况。