6-甲基鸟嘌呤-DNA甲基转移酶和肝脏DNA烷基化在饮食中必需氨基酸缺乏时暴露于二甲基亚硝胺小鼠

Maria Klaude, Alexandra von der Decken
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引用次数: 3

摘要

雄性NMRI小鼠被喂食含有完全氨基酸混合物或缺乏蛋氨酸-半胱氨酸或赖氨酸的混合物(占对照水平的30%),为期6天。在喂养期间,所有小鼠随意饮用含有二甲基亚硝胺的饮用水。暴露量平均为每天每公斤体重1毫克二甲基亚硝胺。测定肝脏提取物中o6 -甲基鸟嘌呤- dna甲基转移酶的浓度。在蛋氨酸-半胱氨酸缺乏的小鼠中显著下降。当分析肝脏DNA的烷基化嘌呤碱基时,小鼠在牺牲前120分钟接受单剂量的14c标记的二甲基亚硝胺(0.5或1 mg/kg体重)。饲喂缺乏赖氨酸饲粮后,o6 -甲基鸟嘌呤浓度显著高于对照组水平,在赖氨酸缺乏6 d后,再饲喂赖氨酸2 d, o6 -甲基鸟嘌呤浓度恢复到对照组水平。o6 -甲基鸟嘌呤与N-7-甲基鸟嘌呤比例的增加表明,N-7位点鸟嘌呤的甲基化不受饮食缺乏期间二甲基亚硝胺摄入量的影响。结果表明,为了维持细胞中o6 -甲基鸟嘌呤-DNA甲基转移酶的足够浓度,从而在暴露于二甲基亚硝胺后有效去除DNA中鸟嘌呤O-6位置的甲基,饲粮中氨基酸组成必须保持平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
O6-Methylguanine-DNA methyltransferase and alkylation of liver DNA in mice exposed to dimethylnitrosamine during dietary deficiency of essential amino acids

Male NMRI mice were fed a diet containing a complete mixture of amino acids or a mixture deficient in methionine-cysteine or lysine (30% of the control level) for a period of 6 days. During the feeding period all mice received dimethylnitrosamine in the drinking water ad libitum. The exposure avaraged 1 mg dimethylnitrosamine/kg body weight and day. The concentration of O6-methylguanine-DNA methyltransferase was measured in liver extracts. It decreased significantly in the methionine-cysteine deficient mice. When DNA from the liver was analyzed for alkylated purine bases the mice received a single dose of 14C-labeled dimethylnitrosamine (0.5 or 1 mg/kg body weight)_at 120 min before sacrifice. The concentration of O6-methylguanine increased significantly over the control level upon feeding the deficient diets and was restored to the concentration of the controls by refeeding lysine for 2 days following 6 days of lysine deficiency. The increased ration of O6-methylguanine to N-7-methylguanine indicated that methylation of guanine in the N-7 position was not subject to variation by the intake of dimethylnitrosamine during the dietary deficiencies. The results demonstrate the requirement for a balanced composition of amino acids in the diet to maintain a sufficient concentration of O6-methylguanine-DNA methyltransferase in the cells and thus to permit efficient removal of the methyl group from the O-6 position of guanine in DNA after exposure to dimethylnitrosamine.

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