Effects of neurosteroid 3α-hydroxy-5α-pregnan-20-one on ethanol-mediated paired-pulse depression of population spikes in the CA1 region of rat hippocampal slices

Abstract

While it is known that ethanol augments GABA-A receptor mediated inhibition in the central nervous system (CNS), demonstrating direct effects of ethanol on GABA transmission has been difficult in brain slices, suggesting that these preparations may lack factors that are required for ethanol's actions. Recent studies indicate that the GABA-enhancing neurosteroid 3α-hydroxy-5α- pregnan-20-one (3α5αP) mediates at least some effects of ethanol in the CNS. In the CA1 region of rat hippocampal slices, we found that 60 mM ethanol failed to alter paired pulse depression (PDD) of population spikes (PSs) when paired stimuli were delivered to the Schaffer collateral pathway at an interval of 21 ms. Following 2-h preincubation of slices with 100 nM 3α5αP, however, ethanol augmented PS PPD. This effect was not observed in the presence of picrotoxin, a GABA-A receptor antagonist, or ADVASEP-7, a β-cyclodextrin that binds 3α5αP. These results indicate that 3α5αP modulates the inhibitory effects of ethanol on hippocampal excitability via GABA-A receptors. © 2005 Elsevier Ireland Ltd. All rights reserved.