Anxiolytic activity of the progesterone metabolite 5α-pregnan-3α-ol-20-one

3α-hydroxylated pregnane steroids have been shown to possess anesthetic, hypnotic, anticonvulsant and anxiolytic properties. In this study, metabolites of progesterone and deoxycorticosterone, 5α-pregnan-3α-ol-20-one (3α-OH-DHP) and 5α-pregnan-3α,21-diol-20-one (5α-THDOC), respectively, were tested...

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Veröffentlicht in:Brain research 1991-11, Vol.565 (2), p.263-268
Hauptverfasser: Wieland, Scott, Lan, Nancy C., Mirasedeghi, Seid, Gee, Kelvin W.
Format: Artikel
Sprache:eng
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Zusammenfassung:3α-hydroxylated pregnane steroids have been shown to possess anesthetic, hypnotic, anticonvulsant and anxiolytic properties. In this study, metabolites of progesterone and deoxycorticosterone, 5α-pregnan-3α-ol-20-one (3α-OH-DHP) and 5α-pregnan-3α,21-diol-20-one (5α-THDOC), respectively, were tested for anxiolytic effects in N.I.H. Swiss-Webster mice using the light/dark transition, open-field and lick-suppression tests. Similar to the benzodiazepine (BZ) diazepam, 3α-OH-DHP (5–40 mg/kg) and 5α-THDOC (5–40 mg/kg) significantly increased the number of light/dark transitions. 3α-OH-DHP's effects were stereospecific as its diasteriomer, 3β-OH-DHP was devoid of activity. The benzodiazepine antagonist CGS-8216 (10 mg/kg) blocked diazepam's (1.0 mg/kg) anxiolytic effects, but did not have any effect against 3α-OH-DHP (20 mg/kg). The data indicate that the pregnane steroids produce their anxiolytic effects through a separate mechanism than the BZs. 3α-OH-DHP (20 mg/kg), 5α-THDOC (20 mg/kg) and diazepam (1.0 mg/kg) increased activity in a open-field test. 3β-OH-DHP had no effect in the open-field test. Furthermore, 3α-OH-DHP produced a 235% increase in punished responding in a lick-suppression test. These results demonstrate that the endogenous pregnane steroids possess anxiolytic effects that may be clinically relevant.
ISSN:0006-8993
1872-6240
DOI:10.1016/0006-8993(91)91658-N