Rad M, Hümpel M, Schaefer O, Schoemaker R C, Schleuning W-D, Cohen A F, Burggraaf J
Centre for Human Drug Research, Leiden, The Netherlands.
Br J Clin Pharmacol. 2006 Sep;62(3):288-96. doi: 10.1111/j.1365-2125.2006.02656.x.
Pre-clinical data suggest that the racemic phyto-oestrogen 8-prenylnaringenin (8-PN) may have beneficial effects in postmenopausal women and may become an alternative to classical hormone replacement therapy (HRT) treatment regimes. The aim of this study was to investigate the pharmacokinetics, endocrine effects and tolerability of chemically synthesized 8-PN in postmenopausal women.
The study was performed using a randomized, double-blind, placebo-controlled, dose-escalation design with three groups of eight healthy postmenopausal women. In each group six subjects received 8-PN and two subjects placebo. 8-PN was given orally in doses of 50, 250 or 750 mg. Drug concentrations in serum, urine and faeces were measured up to 48 h and follicle-stimulating hormone/luteinizing hormone (LH) concentrations up to 24 h.
All treatments were well tolerated and associated with a low incidence of (drug unrelated) adverse events. Serum concentrations of free 8-PN showed rapid drug absorption and secondary peaks suggestive of marked enterohepatic recirculation. Independent of the treatment group, approximately 30% of the dose was recovered in excreta as free compound or conjugates over the 48-h observation period. The first C(max) and AUC(0-48 h) showed dose linearity with ratios of 1 : 4.5 : 13.6 (C(max)) and 1 : 5.2 : 17.1 (AUC). The750- mg dose decreased LH concentrations by 16.7% (95% confidence interval 0.5, 30.2).
Single oral doses of up to 750 mg 8-PN were well tolerated by postmenopausal women. The pharmacokinetic profile of 8-PN was characterized by rapid and probably complete enteral absorption, high metabolic stability, pronounced enterohepatic recirculation and tight dose linearity. The decrease in LH serum concentrations found after the highest dose demonstrates the ability of 8-PN to exert systemic endocrine effects in postmenopausal women.
临床前数据表明,消旋植物雌激素8-异戊烯基柚皮素(8-PN)可能对绝经后女性有益,并且可能成为经典激素替代疗法(HRT)治疗方案的替代选择。本研究的目的是调查化学合成的8-PN在绝经后女性中的药代动力学、内分泌效应和耐受性。
本研究采用随机、双盲、安慰剂对照、剂量递增设计,分为三组,每组8名健康绝经后女性。每组中,6名受试者接受8-PN,2名受试者接受安慰剂。8-PN口服给药,剂量分别为50、250或750mg。在长达48小时内测定血清、尿液和粪便中的药物浓度,在长达24小时内测定促卵泡激素/促黄体生成素(LH)浓度。
所有治疗耐受性良好,(与药物无关的)不良事件发生率较低。游离8-PN的血清浓度显示药物吸收迅速,且有继发性峰,提示明显的肠肝循环。与治疗组无关,在48小时观察期内,约30%的剂量以游离化合物或结合物形式在排泄物中回收。首个C(max)和AUC(0 - 48 h)显示出剂量线性关系,比值分别为1 : 4.5 : 13.6(C(max))和1 : 5.2 : 17.1(AUC)。750mg剂量使LH浓度降低了16.7%(95%置信区间0.5, 30.2)。
绝经后女性对单次口服高达750mg的8-PN耐受性良好。8-PN的药代动力学特征为肠道吸收迅速且可能完全,代谢稳定性高,肠肝循环明显,剂量线性关系紧密。最高剂量后LH血清浓度的降低证明了8-PN在绝经后女性中发挥全身内分泌效应的能力。