Proceedings of the National Academy of Sciences · 1991 · 960 citations · 38 references
Life SciencesNeurobiologyNeuroscienceNeurochemistryNeuroendocrinologySteroid BiochemistryAdrenal Steroid HormonesGabaergic NeurochemistryGabaergic SignalingGonadal HormonesGonadal Steroid HormonesStress EndocrinologyAcute StressGaba Receptor SignalingGaba-a Receptor PharmacologyGamma-aminobutyric Acid Type A Receptor ModulationStress-induced Steroidogenesis
A 3 alpha-hydroxy A-ring-reduced metabolite of progesterone, 3 alpha-hydroxy-5 alpha-pregnan-20-one (allopregnanolone), and one of deoxycorticosterone (DOC), 3 alpha,21-dihydroxy-5 alpha-pregnan-20- one (allotetrahydroDOC), are among the most potent known ligands of gamma-aminobutyric acid (GABA) receptors designated GABAA in the central nervous system. With specific radioimmunoassays, rapid (less than 5 min) and robust (4- to 20-fold) increases of allopregnanolone and allotetrahydroDOC were detected in the brain (cerebral cortex and hypothalamus) and in plasma of rats after exposure to ambient temperature swin stress. Neither steroid was detectable in the plasma of adrenalectomized rats either before or after swim stress. However, allopregnanolone, but not allotetrahydroDOC, was still present in the cerebral cortex (greater than 3 ng/g) after adrenalectomy. These data demonstrate the presence of allopregnanolone and allotetrahydroDOC in brain and show that acute stress results in a rapid increase of these neuroactive steroids to levels known to modulate GABAA receptor function.
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