Neurosteroid Effects on GABAergic Synaptic Plasticity in Hippocampus

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Abstract
We have previously reported that short-term (48–72 h) exposure to the GABA-modulatory steroid 3α-OH-5α-pregnan-20-one (3α,5α-THP) increases expression of the α4 subunit of the GABAAreceptor (GABAR) in the hippocampus of adult rats. This change in subunit composition was accompanied by altered pharmacology and an increase in general excitability associated with acceleration of the decay time constant (τ) for GABA-gated current of pyramidal cells acutely isolated from CA1 hippocampus similar to what we have reported following withdrawal from the steroid after chronic long-term administration. Because GABAR can be localized to either synaptic or extrasynaptic sites, we tested the hypothesis that this change in receptor kinetics is mediated by synaptic GABAR. To this end, we evaluated the decay kinetics of TTX-resistant miniature inhibitory postsynaptic currents (mIPSCs) recorded from CA1 pyramidal cells in hippocampal slices following 48-h treatment with 3α,5α/β-THP (10 mg/kg, ip). Hormone treatment produced a marked acceleration in the fast decay time constant (τfast) of GABAergic mIPSCs. This effect was prevented by suppression of α4-subunit expression with antisense (AS) oligonucleotide, suggesting that hormone treatment increases α4-containing GABAR subsynaptically. This conclusion was further supported by pharmacological data from 3α,5β-THP-treated animals, demonstrating a bimodal distribution of τs for individual mIPSCs following bath application of the α4-selective benzodiazepine RO15–4513, with a shift to slower values. Because 40–50% of the individual τs were also shifted to slower values following bath application of the non–α4-selective benzodiazepine agonist lorazepam (LZM), we suggest that the number of GABAR synapses containing α4 subunits is equivalent to those that do not following 48-h administration of 3α,5β-THP. The decrease in GABAR-mediated charge transfer resulting from accelerated current decay may then result in increased excitability of the hippocampal circuitry, an effect consistent with the increased behavioral excitability we have previously demonstrated.