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Vol. 289, Issue 1, 405-411, April 1999
Department of Physiology and Pharmacology, Wake Forest
University School of Medicine, Winston-Salem, North Carolina (C.A.B.,
K.A.G.); and
Department of Neuropharmacology, Scripps
Research Institute, La Jolla, California (R.H.P.)
A number of endogenous steroids exhibit rapid, nongenomic effects on
the central nervous system and are called neuroactive steroids. The
rapid mechanisms of action include modulation of
-aminobutyric acid
type A (GABAA) and
N-methyl-D-aspartate (NMDA) receptors, which
are two receptors implicated in the behavioral effects of ethanol. It
was hypothesized that neuroactive steroids that positively modulate
GABAA receptors or negatively modulate NMDA receptors,
analogous to the actions of ethanol, would produce discriminative
stimulus effects similar to ethanol. Two groups of male Long-Evans rats
(n = 6-8/group) were trained to discriminate between 1.0 or 2.0 g/kg ethanol (i.g.) and water (i.g.). The
neuroactive steroids allopregnanolone, pregnanolone, epipregnanolone,
allotetrahydrodeoxycorticosterone, pregnanolone sulfate,
epipregnanolone sulfate, dehydroepiandrosterone, dehydroepiandrosterone
sulfate, pregnenolone, and pregnenolone sulfate (PS), all administered
i.p., were tested for substitution with acute and cumulative dosing
procedures (n = 4-8/steroid). The
GABAA-positive modulatory steroids allopregnanolone,
pregnanolone, and allotetrahydrodeoxycorticosterone substituted for
ethanol, as did the low-efficacy steroid 3
,5
-P.
GABAA-negative modulators, such as dehydroepiandrosterone
sulfate and PS, and all of the NMDA modulators tested, including PS,
pregnanolone sulfate, and epipregnanolone sulfate, did not substitute
for ethanol. These results show that certain endogenously occurring
neuroactive steroids produce discriminative stimulus effects similar to
those of ethanol.
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