Tsambaos D, Bolsen K, Georgiou S, Kalofoutis A, Goerz G
Department of Dermatology, University of Patras, Greece.
Skin Pharmacol. 1994;7(6):320-3. doi: 10.1159/000211313.
Doses of 3 and 10 mg/kg/day acitretin were orally administered to female Wistar rats over a period of 6 weeks. Phospholipid classes, P-450 content, aminopyrine-N-demethylase (ADM) and 7-ethoxyresorufin-O-deethylase (7-ERO-D) activities were determined in the liver microsomes of the treated animals. Both dosages caused statistically significant alterations in rat liver microsomal phospholipid composition which may be associated with changes in the metabolic activity, ionic transport, cell-cell interaction and other processes of the hepatic cellular components. Furthermore, statistically significant alterations of P-450 isozyme activities were induced by both dosages. Our data suggest a possible interaction of acitretin with other drugs and endogenous substances metabolized by these enzyme systems.
在6周的时间里,给雌性Wistar大鼠口服3毫克/千克/天和10毫克/千克/天的阿维A剂量。测定了受试动物肝脏微粒体中的磷脂类别、P - 450含量、氨基比林 - N - 脱甲基酶(ADM)和7 - 乙氧基异吩恶唑酮 - O - 脱乙基酶(7 - ERO - D)活性。两种剂量均引起大鼠肝脏微粒体磷脂组成的统计学显著变化,这可能与代谢活性、离子转运、细胞间相互作用以及肝细胞成分的其他过程的变化有关。此外,两种剂量均诱导了P - 450同工酶活性的统计学显著变化。我们的数据表明阿维A可能与这些酶系统代谢的其他药物和内源性物质相互作用。