Lack of influence of menstrual cycle and premenstrual syndrome diagnosis on pregnanolone pharmacokinetics

被引:16
作者
Sundström, I [1 ]
Spigset, O
Andersson, A
Appelblad, P
Bäckström, T
机构
[1] Umea Univ Hosp, Dept Obstet & Gynaecol, S-90185 Umea, Sweden
[2] Reg & Univ Hosp, Dept Clin Pharmacol, Trondheim, Norway
[3] Umea Univ, Div Clin Pharmacol, Umea, Sweden
[4] Umea Univ, Dept Physiol, S-90187 Umea, Sweden
[5] Umea Univ, Dept Analyt Chem, S-90187 Umea, Sweden
关键词
pregnanolone; pharmacokinetics; premenstrual syndrome;
D O I
10.1007/s002280050606
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Pregnanolone is a 3 alpha-hydroxylated-5 beta-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. Methods: 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. Results: Mean pregnanolone elimination half-life varied between 28.4 min and 31.8 min and clearance between 59.6 ml . min(-1) . kg(-1) and 64.0 ml . min(-1) . 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. Conclusion: Pregnanolone pharmacokinetics do not differ between follicular and luteal phase of the menstrual cycle, nor between PMS patients and control subjects.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 28 条
[1]  
*AM PSYCH ASS, 1994, DIAGN STAT MAN MENT, P714
[2]   Determination of C-21 ketosteroids in serum using trifluoromethanesulfonic acid catalyzed precolumn dansylation and 1,1′-oxalyldiimidazole postcolumn peroxyoxalate chemiluminescence detection [J].
Appelblad, P ;
Jonsson, T ;
Bäckström, T ;
Irgum, K .
ANALYTICAL CHEMISTRY, 1998, 70 (23) :5002-5009
[3]   PHARMACOKINETIC DRUG-INTERACTIONS WITH ORAL-CONTRACEPTIVES [J].
BACK, DJ ;
ORME, MLE .
CLINICAL PHARMACOKINETICS, 1990, 18 (06) :472-484
[4]   PULSATILE SECRETION OF LH, FSH, PROLACTIN, ESTRADIOL AND PROGESTERONE DURING THE HUMAN MENSTRUAL-CYCLE [J].
BACKSTROM, CT ;
MCNEILLY, AS ;
LEASK, RM ;
BAIRD, DT .
CLINICAL ENDOCRINOLOGY, 1982, 17 (01) :29-42
[5]   PHARMACOKINETICS AND PHARMACODYNAMICS OF ELTANOLONE (PREGNANOLONE), A NEW STEROID INTRAVENOUS ANESTHETIC, IN HUMANS [J].
CARL, P ;
HOGSKILDE, S ;
LANGJENSEN, T ;
BACH, V ;
JACOBSEN, J ;
SORENSEN, MB ;
GRALLS, M ;
WIDLUND, L .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1994, 38 (07) :734-741
[6]   PREGNANOLONE EMULSION - A PRELIMINARY PHARMACOKINETIC AND PHARMACODYNAMIC STUDY OF A NEW INTRAVENOUS ANESTHETIC AGENT [J].
CARL, P ;
HOGSKILDE, S ;
NIELSEN, JW ;
SORENSEN, MB ;
LINDHOLM, M ;
KARLEN, B ;
BACKSTROM, T .
ANAESTHESIA, 1990, 45 (03) :189-197
[7]  
COPRECHOT C, 1993, ENDOCRINOLOGY, V133, P1003
[8]  
CORDARO JA, 1993, PHARMACOTHERAPY, V13, P369
[9]  
DALE O, 1998, NORW SOC PHARM TOX 2
[10]   PRELIMINARY-STUDY OF A PREGNANOLONE EMULSION (KABI-2213) FOR IV INDUCTION OF GENERAL-ANESTHESIA [J].
GRAY, HS ;
HOLT, BL ;
WHITAKER, DK ;
EADSFORTH, P .
BRITISH JOURNAL OF ANAESTHESIA, 1992, 68 (03) :272-276