Margison G P
Carcinogenesis. 1981;2(5):431-4. doi: 10.1093/carcin/2.5.431.
The capacity of rat liver to repair O6-methylguanine was determined by measuring the amounts of this base present in DNA after administration of N-[14C]methyl-N-nitrosourea (MNU). Chronic pretreatment of animals with unlabelled MNU either once weekly for 5 weeks or daily on weekdays for 14 days had either no marked effect or inhibited (or overloaded) repair activity, respectively. Pretreatment of rats with single doses of MNU initially decreased O6-methylguanine repair but this effect was lost as the pretreatment interval increased and by 40 h, activity had returned to control values. Administration of methylmethanesulphonate for 14 days had no effect on the removal of O6-methylguanine produced in liver DNA by [14C]MNU. None of the pretreatment schedules inhibited the removal of 3-methyladenine from liver DNA. These effects are contrasted with those produced by pretreatment of rats with dimethylnitrosamine (DMN) or 1,2-dimethylhydrazine which enhanced the capacity of the liver to remove O6-methylguanine produced by single dose of [14C]DMN.
通过测量给予N-[¹⁴C]甲基-N-亚硝基脲(MNU)后DNA中该碱基的含量,来确定大鼠肝脏修复O⁶-甲基鸟嘌呤的能力。用未标记的MNU对动物进行慢性预处理,每周一次,共5周,或在工作日每天进行,共14天,分别对修复活性没有明显影响或抑制(或使其过载)。用单剂量MNU预处理大鼠最初会降低O⁶-甲基鸟嘌呤的修复,但随着预处理间隔时间的增加,这种效果会消失,到40小时时,活性已恢复到对照值。给予甲磺酸甲酯14天,对[¹⁴C]MNU在肝脏DNA中产生的O⁶-甲基鸟嘌呤的去除没有影响。没有一种预处理方案能抑制肝脏DNA中3-甲基腺嘌呤的去除。这些效果与用二甲基亚硝胺(DMN)或1,2-二甲基肼预处理大鼠所产生的效果形成对比,后者增强了肝脏去除单剂量[¹⁴C]DMN产生的O⁶-甲基鸟嘌呤的能力。