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Serum Profiles of Free and Conjugated Neuroactive Pregnanolone Isomers in Nonpregnant Women of Fertile Age

Helena Havlíková, Martin Hill, Lyudmila Kancheva, Jana Vrbíková, Vladimír Pouzar, Ivan ern, Radmila Kancheva and Luboslav Stárka

Institute of Endocrinology (H.H., M.H., L.K., J.V., R.K., L.S.), CZ 116 94 Prague, Czech Republic; and Institute of Organic Chemistry and Biochemistry (V.P., I.), CZ 166 10 Prague, Czech Republic

Address all correspondence and requests for reprints to: Dr. Martin Hill, Institute of Endocrinology, Národní tida 8, CZ 116 94 Prague 1, Czech Republic. E-mail: mhill{at}endo.cz.

Background: Pregnanolone isomers (PI) with a hydroxy group in the 3-position are neuroinhibitors operating via positive modulation of GABA_A receptors. The 3ß-PI and sulfates of PI and pregnenolone exert the opposite effect. In addition to the brain’s in situ synthesis, some circulating steroids can penetrate the blood-brain barrier.

Methods: To assess the physiological impact of peripheral endogenous neuroactive pregnanolone isomers and their polar conjugates in women, serum allopregnanolone (P35), isopregnanolone (P3ß5), pregnanolone (P35ß), epipregnanolone (P3ß5ß), pregnenolone, estradiol (including their polar conjugates), and additional steroids were measured in 16 women in the follicular and luteal phases of the menstrual cycle using gas chromatography/mass spectrometry and RIA for the analysis. Linear models and Spearman’s correlations were used for data evaluation.

Results and Discussion: The levels of conjugated PI were from one to almost three orders of magnitude higher in comparison with the free steroids. The results indicate that a substantial proportion of the progesterone is metabolized in the sequence progesterone5ß-dihydroprogesteroneP35ßconjugated P35ß. The sulfation of PI and particularly of P35ß moderates the levels of free PI and restrains estradiol biosynthesis via progesterone degradation. PI including the conjugates reflected changing progesterone formation during the menstrual cycle. In the follicular phase, the positive correlation with conjugated pregnenolone, the independence of progesterone, and the negative age relationships of PI indicate their adrenal origin. The dependence on progesterone and the independence of conjugated pregnenolone suggest a gonadal source of PI in the luteal phase. The neuroactivating PI prevailed over neuroinhibiting PI.

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