Golikov P P, Kladiev A A, Nikolaeva N Iu
Farmakol Toksikol. 1989 Jul-Aug;52(4):52-5.
The experiments were performed on intact and phlogogenically exposed male Wistar rats (weighing 180-210 g). Glucocorticoid receptors were determined in a high-rate cytosol of the liver by using 3H-acetonide triamcinolone. Inflammation was induced by subplantar administration of formalin. In the model experiments, analgin (10(-2) M) decreased the level of glucocorticoid receptors in the rat liver cytosol. In a dose of 250 mg/kg intraperitoneally, analgin after 90 min decreased the liver content of glucocorticoid receptors and blood plasma concentrations of corticosterone in intact and phlogogenically exposed rats. The mechanism of the decrease of the content of glucocorticoid receptors in the liver and blood plasma concentrations of corticosterone in analgin-treated animals is discussed.
实验在完整的和经致炎剂处理的雄性Wistar大鼠(体重180 - 210克)上进行。通过使用3H - 曲安奈德在肝脏的高速上清液中测定糖皮质激素受体。通过足底注射福尔马林诱导炎症。在模型实验中,安乃近(10^(-2) M)降低了大鼠肝脏胞浆中糖皮质激素受体的水平。腹腔注射剂量为250 mg/kg时,安乃近在90分钟后降低了完整的和经致炎剂处理的大鼠肝脏中糖皮质激素受体的含量以及血浆中皮质酮的浓度。讨论了安乃近处理的动物肝脏中糖皮质激素受体含量降低以及血浆中皮质酮浓度降低的机制。