Sundström I, Spigset O, Andersson A, Appelblad P, Bäckström T
Department of Obstetrics and Gynaecology, University Hospital of Umeå, Sweden.
Eur J Clin Pharmacol. 1999 Apr;55(2):125-30. doi: 10.1007/s002280050606.
Pregnanolone is a 3alpha-hydroxylated-5beta-reduced metabolite of the female sex steroid hormone progesterone. The compound is currently being evaluated for anaesthetic purposes. Previous studies have indicated a differential physiological response across the menstrual cycle and a different response in patients with premenstrual syndrome (PMS). This study was undertaken to determine whether hormonal changes during the menstrual cycle influence pregnanolone pharmacokinetics and to compare PMS diagnosis-related differences in pregnanolone pharmacokinetics.
Seven patients with premenstrual syndrome and seven female controls were given three increasing doses of pregnanolone in the follicular and luteal phase of the menstrual cycle.
Mean pregnanolone elimination half-life varied between 28.4 min and 31.8 min and clearance between 59.6 ml x min(-1) x kg(-1) and 64.0 ml x min(-1) x kg(-1), depending on diagnostic group and cycle phase. No significant differences in pregnanolone pharmacokinetic properties were found between PMS patients and controls in either phase of the menstrual cycle. Furthermore, no differences in pharmacokinetic variables were detected between cycle phases.
Pregnanolone pharmacokinetics do not differ between follicular and luteal phase of the menstrual cycle, nor between PMS patients and control subjects.
孕烷醇酮是女性甾体激素孕酮的一种3α-羟基化-5β-还原代谢产物。目前正在对该化合物进行麻醉用途评估。既往研究表明,其在整个月经周期中存在不同的生理反应,且在经前综合征(PMS)患者中反应也有所不同。本研究旨在确定月经周期中的激素变化是否会影响孕烷醇酮的药代动力学,并比较与PMS诊断相关的孕烷醇酮药代动力学差异。
7例经前综合征患者和7例女性对照在月经周期的卵泡期和黄体期接受了3次递增剂量的孕烷醇酮。
根据诊断组和周期阶段不同,孕烷醇酮的平均消除半衰期在28.4分钟至31.8分钟之间变化,清除率在59.6 ml·min⁻¹·kg⁻¹至64.0 ml·min⁻¹·kg⁻¹之间。在月经周期的任何一个阶段,PMS患者和对照组之间的孕烷醇酮药代动力学特性均未发现显著差异。此外,在不同周期阶段未检测到药代动力学变量的差异。
月经周期的卵泡期和黄体期之间,以及PMS患者与对照受试者之间,孕烷醇酮的药代动力学无差异。