Conradt P, Green U
J Cancer Res Clin Oncol. 1982;104(1-2):53-61. doi: 10.1007/BF00402053.
Dealkylation of diethylnitrosamine (DEN) by a liver microsomal fraction was measured after treatment of the Mongolian gerbil with DEN, Valium, or DEN plus Valium. Valium-dosed male and female animals showed strongly stimulated deethylase levels compared with the controls. This was also true of the DEN-treated females. Combined treatment (DEN + Valium) resulted in a significant loss of activity compared with treatment with DEN only, but was not significantly lower than that in the controls. Significant differences were also found between the experimental groups in microsomal enzymes. Metabolism of 14C-DEN to 14CO2 by gerbil liver slices in vitro showed dose-dependent inhibition by Valium. Kinetic analysis of DEN-dealkylation by purified gerbil microsomes revealed at least two Km values. In the microsomal system, diazepam inhibited DEN-dealkylation significantly at low substrate levels.
在用二乙基亚硝胺(DEN)、安定或DEN加安定处理蒙古沙鼠后,测定了肝微粒体部分对DEN的脱烷基作用。与对照组相比,给予安定的雄性和雌性动物显示出脱乙基酶水平受到强烈刺激。给予DEN的雌性动物也是如此。联合处理(DEN + 安定)与仅用DEN处理相比,导致活性显著丧失,但并不显著低于对照组。在微粒体酶方面,实验组之间也发现了显著差异。体外沙鼠肝切片将14C-DEN代谢为14CO2显示出安定的剂量依赖性抑制作用。对纯化的沙鼠微粒体进行DEN脱烷基作用的动力学分析揭示了至少两个Km值。在微粒体系统中,地西泮在低底物水平时显著抑制DEN脱烷基作用。