Lang M, Marselos M, Törrönen R
Chem Biol Interact. 1976 Nov;15(3):267-76. doi: 10.1016/0009-2797(76)90152-6.
Disulfiram and diethyldithiocarbamate were administered to rats for 4 days alone (300 mg/kg, daily, per os) or in combination with phenobarbital (80 mg/kg, daily, i.p.), in order to observe the effects of these compounds on the microsomal membrane components and on the mixed-function oxygenase system. Both disulfiram and diethyldithiocarbamate increased the liver to body weight ratio, and the total hepatic protein content. Disulfiram significantly increased also the microsomal protein and phospholipid contents. Diethyldithiocarbamate and disulfiram partially prevented the increase of microsomal protein and phospholipid contents caused by phenobarbital. Disulfiram and diethyldithiocarbamate decreased the amount of cytochrome P-450 and P-420, and the activity of p-nitroanisole O-demethylase. These changes were more pronounced after diethyldithiocarbamate than after disulfiram treatment. On the contrary, the activity of NADPH-cytochrome c reductase was enhanced only by disulfiram. The induction by phenobarbital of cytochrome P-450 and p-nitrosanisole O-demethylase was partially prevented on concomitant treatment with disulfiram and diethyldithiocarbamate. These compounds. however, had an additive effect with phenobarbital in enhancing the microsomal NADPH-cytochrome c reductase activity.
将双硫仑和二乙基二硫代氨基甲酸盐单独(300毫克/千克,每日,经口)或与苯巴比妥(80毫克/千克,每日,腹腔注射)联合给予大鼠4天,以观察这些化合物对微粒体膜成分和混合功能氧化酶系统的影响。双硫仑和二乙基二硫代氨基甲酸盐均增加了肝脏与体重的比值以及肝脏总蛋白含量。双硫仑还显著增加了微粒体蛋白和磷脂含量。二乙基二硫代氨基甲酸盐和双硫仑部分阻止了苯巴比妥引起的微粒体蛋白和磷脂含量的增加。双硫仑和二乙基二硫代氨基甲酸盐降低了细胞色素P-450和P-420的含量以及对硝基苯甲醚O-脱甲基酶的活性。二乙基二硫代氨基甲酸盐处理后这些变化比双硫仑处理后更明显。相反,仅双硫仑增强了NADPH-细胞色素c还原酶的活性。在与双硫仑和二乙基二硫代氨基甲酸盐同时处理时,苯巴比妥对细胞色素P-450和对硝基苯甲醚O-脱甲基酶的诱导作用被部分阻止。然而,这些化合物在增强微粒体NADPH-细胞色素c还原酶活性方面与苯巴比妥具有相加作用。