Hong J, Yang C S
Carcinogenesis. 1985 Dec;6(12):1805-9. doi: 10.1093/carcin/6.12.1805.
The subcellular localization of N-nitrosodimethylamine (NDMA) demethylase in rat liver cells and the role of this enzyme in the activation of NDMA were studied. The enzyme activity was predominantly located in the microsomal fraction and the addition of cytosol to the microsomes did not produce a synergistic effect. The microsomal NDMA demethylase activity appeared to correspond to the ability of the microsomes to convert NDMA to the alkylating species. The alkylation of DNA was assayed by the measurement of O6-methylguanine and 7-methylguanine by fluorescence after isolation by h.p.l.c. The induction of microsomal NDMA demethylase activity by isopropanol, ethanol, acetone, and fasting was closely related to the increase of DNA methylation by NDMA in an incubation system in vitro. Pretreatment of rats with ethanol, which induced hepatic NDMA demethylase activity, enhanced DNA alkylation in vivo with a high dose of NDMA (75 mg/kg body weight) but not with low doses of NDMA (less than or equal to 25 mg/kg body weight). The role of NDMA demethylase in the activation of NDMA is discussed.
研究了大鼠肝细胞中N-亚硝基二甲胺(NDMA)脱甲基酶的亚细胞定位及其在NDMA活化中的作用。酶活性主要位于微粒体部分,向微粒体中添加胞质溶胶未产生协同效应。微粒体NDMA脱甲基酶活性似乎与微粒体将NDMA转化为烷基化物质的能力相对应。通过高效液相色谱分离后用荧光法测量O6-甲基鸟嘌呤和7-甲基鸟嘌呤来检测DNA的烷基化。在体外孵育系统中,异丙醇、乙醇、丙酮和禁食对微粒体NDMA脱甲基酶活性的诱导与NDMA导致的DNA甲基化增加密切相关。用乙醇预处理大鼠可诱导肝脏NDMA脱甲基酶活性,高剂量NDMA(75 mg/kg体重)可增强体内DNA烷基化,但低剂量NDMA(小于或等于25 mg/kg体重)则不然。文中讨论了NDMA脱甲基酶在NDMA活化中的作用。