Progesterone metabolite allopregnanolone in women with premenstrual syndrome

被引:246
作者
Rapkin, AJ
Morgan, M
Goldman, L
Brann, DW
Simone, D
Mahesh, VB
机构
[1] UNIV CALIF LOS ANGELES,SCH SOCIAL WORK,LOS ANGELES,CA 90095
[2] MED COLL GEORGIA,DEPT PHYSIOL & ENDOCRINOL,AUGUSTA,GA 30912
关键词
D O I
10.1016/S0029-7844(97)00417-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To evaluate the anxiolytic 3 alpha-5 alpha-reduced progesterone metabolite allopregnanolone in the luteal phase of the menstrual cycle in women with premenstrual syndrome (PMS) and controls. Methods: Thirty-five women with prospectively documented PMS and 36 controls were evaluated. Serum progesterone and allopregnanolone levels were measured on days 19 and 26 of the cycle as determined by urinary LH detection kits. Analysis of variance and Student t tests were used to analyze the data. Results: Allopregnanolone levels were significantly lower on day 26 in the PMS group than in controls (3.6 +/- 0.8 versus 7.5 +/- 1.3 ng/mL; P < .04). Significant differences in the ratio of the metabolite to progesterone also were noted, with a smaller ratio in the PMS subjects (0.9 +/- 0.3 versus 3.2 +/- 1.3 ng/mL; P < .05). There were no significant differences between the PMS and control groups with respect to serum progesterone levels. Conclusion: Subjects with PMS manifested lower levels of the anxiolytic metabolite allopregnanolone in the luteal phase when compared with controls. Diminished concentrations of allopregnanolone in women with PMS may lead to an inability to enhance gamma aminobutyric acid-mediated inhibition during states of altered central nervous system excitability, such as ovulation or physiologic or psychological stress. The lowered metabolite levels could contribute to the genesis of various mood symptoms of the disorder, such as anxiety, tension, and depression. (C) 1997 by The American College of Obstetricians and Gynecologists.
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页码:709 / 714
页数:6
相关论文
共 30 条
[1]  
American Psychiatric Association, 1994, DIAGN STAT MAN MENT
[2]  
BARTHOLINI G, 1986, LERS MONOGRAPH SERIE, V4, P105
[3]   ANXIOLYTIC EFFECTS OF 3A-HYDROXY-5A[BETA]-PREGNAN-20-ONE - ENDOGENOUS METABOLITES OF PROGESTERONE THAT ARE ACTIVE AT THE GABA-A RECEPTOR [J].
BITRAN, D ;
HILVERS, RJ ;
KELLOGG, CK .
BRAIN RESEARCH, 1991, 561 (01) :157-161
[4]   GAMMA-AMINOBUTYRIC ACIDA RECEPTORS MEDIATE 3-ALPHA-HYDROXY-5-ALPHA-PREGNAN-20-ONE-INDUCED GONADOTROPIN-SECRETION [J].
BRANN, DW ;
PUTNAM, CD ;
MAHESH, VB .
ENDOCRINOLOGY, 1990, 126 (04) :1854-1859
[5]   A KEY ENZYME IN THE BIOSYNTHESIS OF NEUROSTEROIDS, 3-BETA-HYDROXYSTEROID DEHYDROGENASE/DELTA(5)DELTA(4)-ISOMERASE (3-BETA-HSD), IS EXPRESSED IN RAT-BRAIN [J].
GUENNOUN, R ;
FIDDES, RJ ;
GOUEZOU, M ;
LOMBES, M ;
BAULIEU, EE .
MOLECULAR BRAIN RESEARCH, 1995, 30 (02) :287-300
[6]  
HARRISON NL, 1987, J PHARMACOL EXP THER, V241, P346
[7]  
HOLZBAUER M, 1976, MED BIOL, V54, P227
[8]   INVIVO SECRETION OF 3-ALPHA-HYDROXY-5-ALPHA-PREGNAN-20-ONE, A POTENT ANESTHETIC STEROID, BY THE ADRENAL-GLAND OF THE RAT [J].
HOLZBAUER, M ;
BIRMINGHAM, MK ;
DENICOLA, AF ;
OLIVERS, JT .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1985, 22 (01) :97-102
[10]   PHYSIOLOGICAL VARIATIONS IN OVARIAN PRODUCTION OF 5-ALPHA-PREGNANE DERIVATIVES WITH SEDATIVE PROPERTIES IN RAT [J].
HOLZBAUER, M .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1975, 6 (09) :1307-1310