Laitinen M, Lang M, Hietanen E, Vainio H
Toxicology. 1975 Sep;5(1):79-88. doi: 10.1016/0300-483x(75)90072-4.
A combined effect of cholesterol and polychlorinated biphenyls (PCBs) on the microsomal drug hydroxylation and glucuronidation in the liver of the rat was studied. PCBs, Clophen A-50 and A-60, having an average chlorination degree of 50 and 60% affect the structure of microsomal membranes. It was found that Clophen A-60 increased the binding of trypsin- and digitonin-sensitive proteins to the membranes. Also it was found that PCBs enhanced the phsopholipid content of microsomes. PCBs increased the activity of hepatic NADPH cytochrome c reductase about 1.5-fold. Aryl hydrocarbon hydroxylase activity doubled with Clophen A-50 and quadrupled with Clophen A-60. Hepatic UDPglucuronosyltransferase activity was doubled with both PCBs. The enhancement in hepatic aryl hydrocarbon hydroxylase and in UDPglucuronosyltransferase was found to be lower in the presence of high cholesterol level in the diet when compared to earlier results. This is supposed to be due to the membraneous effects of cholesterol.
研究了胆固醇和多氯联苯(PCBs)对大鼠肝脏微粒体药物羟基化和葡萄糖醛酸化的联合作用。平均氯化度为50%和60%的PCBs,即氯芬A - 50和A - 60,会影响微粒体膜的结构。发现氯芬A - 60增加了胰蛋白酶和洋地黄皂苷敏感蛋白与膜的结合。还发现PCBs提高了微粒体的磷脂含量。PCBs使肝脏NADPH细胞色素c还原酶的活性增加了约1.5倍。氯芬A - 50使芳烃羟化酶活性加倍,氯芬A - 60使其活性增加四倍。两种PCBs都使肝脏UDP - 葡萄糖醛酸基转移酶活性加倍。与早期结果相比,当饮食中胆固醇水平较高时,肝脏芳烃羟化酶和UDP - 葡萄糖醛酸基转移酶的增强作用较低。这被认为是由于胆固醇的膜效应。