GABAA‐Mediated Toxicity of Hippocampal Neurons In Vitro

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Abstract
In the present study, we examined whether the elevation of GABA by γ-vinyl-GABA protects cultured rat fetal hippocampal neurons against toxicity induced by a 20-min incubation with 100 μM L-glutamate. Neither a 24-h pretreatment nor posttreatment with γ-vinyl-GABA (100 μM) had any neuroprotective effects, as determined by counting microtubule-associated protein-2 positive cells and lactate dehydrogenase assay 24 h after the glutamate treatment. Unexpectedly, γ-vinyl-GABA alone induced a 20% loss of microtubule-associated protein-2-positive cells in a culture that was grown in medium containing 25 mM KCl. The toxic effect of γ-vinyl-GABA was mimicked by a 24-h treatment with GABA (100 μM) and the GABAA receptor agonist, muscimol (10 μM), but not the GABAB receptor agonist, baclofen (10 μM). The GABAA receptor antagonist, bicuculline (10 μM), protected against γ-vinyl-GABA and GABA-evoked toxicity. Neither γ-vinyl-GABA nor GABA was toxic in culture medium containing 15 mM KCl. These data indicate that, under depolarizing conditions, an increased GABA level is toxic for a subpopulation of developing hippocampal neurons in vitro. The effect is GABAA receptor-mediated. These data provide a new view for understanding neurodegenerative processes, and raise a question of the safety of therapies aimed at increasing GABA concentration following brain insults, especially in immature brains.