Grafström R, Holmberg B
Toxicol Lett. 1980 Nov;7(1):79-85. doi: 10.1016/0378-4274(80)90088-0.
Disulfiram (DS) was administered perorally once a day to rats for 30 days to investigate the effects on cytochrome P-450 content and benzo(a)pyrene (BP) monooxygenase activity in microsomes isolated from the small intestinal mucosa. 50 mg or 100 mg DS/kg body weight caused a dose-related increase in BP monooxygenase activity, whereas the content of cytochrome P-450 was increased at the higher dose only. Similar absorption characteristics of cytochrome P-450 and turnover rates for BP on the basis o f cytochrome P-450 was observed among the different microsomal preparations. The addition of DS or diethyldithiocarbamate (DDTC) to incubates of intestinal microsomes inhibited BP monooxygenase activity. Microsomes isolated from DS-treated rats were however less sensitive to in vitro inhibition by DS.
每天给大鼠口服双硫仑(DS),持续30天,以研究其对从小肠黏膜分离的微粒体中细胞色素P - 450含量和苯并(a)芘(BP)单加氧酶活性的影响。50毫克或100毫克DS/千克体重导致BP单加氧酶活性呈剂量相关增加,而细胞色素P - 450含量仅在较高剂量时增加。在不同的微粒体制剂中观察到基于细胞色素P - 450的细胞色素P - 450相似吸收特性和BP周转率。向肠道微粒体孵育物中添加DS或二乙基二硫代氨基甲酸盐(DDTC)可抑制BP单加氧酶活性。然而,从经DS处理的大鼠分离的微粒体对DS的体外抑制作用不太敏感。