Frey B M, Schaad H J, Frey F J
Eur J Clin Pharmacol. 1984;26(4):505-11. doi: 10.1007/BF00542149.
The oestrogenic component of oral contraceptives affects the activity of liver enzymes and the concentrations of plasma proteins implicated in steroid metabolism and transport. The present study was designed to determine these effects on the kinetics of prednisone and prednisolone. After an oral dose of prednisone, women on oral contraceptive steroids (n = 10) had higher mean (+/- SD) area under the plasma concentration versus time curves of total (428 +/- 67 micrograms/ml/min vs 188 +/- 28 micrograms/ml/min, p less than 0.001) and unbound prednisolone (64 +/- 10 micrograms/ml/min vs 41 +/- 10 micrograms/ml/min, p less than 0.001) than women not taking oral contraceptive steroids (n = 10). The differences were attributable to a lower non-renal clearance of prednisolone and to a higher apparent systemic availability of the drug in contraceptive users than in the controls. The affinity of albumin and transcortin for prednisolone was lower in women on oral contraceptives than in controls (p less than 0.001). Thus, altered kinetics and protein binding may account for the known increase in glucocorticoid efficacy by oestrogens.
口服避孕药中的雌激素成分会影响肝脏酶的活性以及与类固醇代谢和转运相关的血浆蛋白浓度。本研究旨在确定其对泼尼松和泼尼松龙动力学的影响。口服一剂泼尼松后,服用口服避孕类固醇的女性(n = 10)的总泼尼松龙(428 +/- 67微克/毫升/分钟对188 +/- 28微克/毫升/分钟,p < 0.001)和游离泼尼松龙(64 +/- 10微克/毫升/分钟对41 +/- 10微克/毫升/分钟,p < 0.001)血浆浓度-时间曲线下的平均(+/-标准差)面积高于未服用口服避孕类固醇的女性(n = 10)。这些差异归因于泼尼松龙较低的非肾清除率以及避孕药使用者中该药物较高的表观全身可用性。口服避孕药的女性中,白蛋白和皮质素结合球蛋白对泼尼松龙的亲和力低于对照组(p < 0.001)。因此,动力学和蛋白质结合的改变可能解释了雌激素导致糖皮质激素疗效增加的已知现象。