Bradamante V, Kunec-Vajić E
Department of Pharmacology, Faculty of Medicine, University of Zagreb, Yugoslavia.
Biomed Biochim Acta. 1987;46(6):439-43.
Changes in plasma cholinesterase (ChE) activity after administration of glucocorticoids (prednisone, methyl-prednisolone and dexamethasone) were studied in male and female rats. The decrease of ChE activity-probably due to inhibition of ChE synthesis in the liver-was more marked in female than in male rats. This difference could be explained by the more rapid metabolism of glucocorticoids in male than in female rats or by the decreased stimulatory effect of estrogens on ChE synthesis after administration of glucocorticoids. The inhibitory effect of dexamethasone on ChE synthesis was significantly greater than the effect of equivalent antiinflammatory doses of the other two glucocorticoids investigated. The inhibitory effect of glucocorticoids on ChE activity increased with the duration of their administration. Decrease of ChE activity was more marked after the p.o. than after the i.p. route of application, indicating that inhibition of ChE synthesis after p.o. administration of glucocorticoids occurs partially during the first pass of these drugs in the liver.
在雄性和雌性大鼠中研究了给予糖皮质激素(泼尼松、甲泼尼龙和地塞米松)后血浆胆碱酯酶(ChE)活性的变化。ChE活性的降低——可能是由于肝脏中ChE合成受到抑制——在雌性大鼠中比在雄性大鼠中更明显。这种差异可以通过雄性大鼠中糖皮质激素的代谢比雌性大鼠更快,或者通过给予糖皮质激素后雌激素对ChE合成的刺激作用降低来解释。地塞米松对ChE合成的抑制作用明显大于所研究的其他两种等效抗炎剂量糖皮质激素的作用。糖皮质激素对ChE活性的抑制作用随着给药时间的延长而增加。口服给药后ChE活性的降低比腹腔注射给药后更明显,这表明口服糖皮质激素后ChE合成的抑制部分发生在这些药物在肝脏的首过过程中。