Kyrtopoulos S A, Hadjiloucas E, Vrotsou B
Cancer Res. 1982 May;42(5):1962-6.
Cimetidine was administered by stomach tube to rats at 70 or 700 mg/kg, doses corresponding to 5 or 50 times, respectively, the typical daily dose of individuals on cimetidine treatment. In some cases, cimetidine (70 mg/kg) was administered in combination with a 2-fold molar excess of sodium nitrite. This treatment was carried out up to 6 times over a 3-day period, the pH of the rat stomach being maintained at 2.3 to 3.0 for about 1 hr after each treatment. The DNA of the stomach, liver, and intestines (large and small pooled together) was isolated 6 hr after cessation of treatment and analyzed for the presence of O6-methylguanine using a sensitive and specific radioimmunoassay. No evidence could be obtained for the presence of this methylated base in any of the DNA samples examined, the limit of detection being 3 mumol O6-methylguanine per mol guanine. We suggest that the observed lack of DNA methylation may be primarily due to the slow rate of nitrosation of cimetidine in combination with its rapid absorption into the blood stream.
用胃管给大鼠分别按70或700mg/kg的剂量灌胃西咪替丁,这两个剂量分别相当于接受西咪替丁治疗的个体典型日剂量的5倍或50倍。在某些情况下,西咪替丁(70mg/kg)与两倍摩尔过量的亚硝酸钠联合给药。这种处理在3天内进行多达6次,每次处理后大鼠胃的pH维持在2.3至3.0约1小时。在停止处理6小时后,分离胃、肝和肠(大小肠合并)的DNA,并使用灵敏且特异的放射免疫测定法分析O6-甲基鸟嘌呤的存在情况。在所检测的任何DNA样品中均未获得该甲基化碱基存在的证据,检测限为每摩尔鸟嘌呤3μmol O6-甲基鸟嘌呤。我们认为,观察到的DNA甲基化缺乏可能主要是由于西咪替丁亚硝化速率缓慢及其快速吸收进入血流所致。