Neuroactive steroids reduce neuronal excitability by selectively enhancing tonic inhibition mediated by δ subunit-containing GABA _A receptors

TLDR

Neuroactive steroids modulate GABA_A receptors and fluctuations in their levels are linked to premenstrual syndrome, postpartum depression, and anxiety disorders. Neuroactive steroids selectively enhance tonic inhibition through δ‑subunit GABA_A receptors, reducing neuronal excitability and offering a potential therapeutic target for mood disorders.

Abstract

Neuroactive steroids are potent modulators of γ-aminobutyric acid type A receptors (GABA A Rs), and their behavioral effects are generally viewed in terms of altered inhibitory synaptic transmission. Here we report that, at concentrations known to occur in vivo , neuroactive steroids specifically enhance a tonic inhibitory conductance in central neurons that is mediated by extrasynaptic δ subunit-containing GABA A Rs. The neurosteroid-induced augmentation of this tonic conductance decreases neuronal excitability. Fluctuations in the circulating concentrations of endogenous neuroactive steroids have been implicated in the genesis of premenstrual syndrome, postpartum depression, and other anxiety disorders. Recognition that δ subunit-containing GABA A Rs responsible for a tonic conductance are a preferential target for neuroactive steroids may lead to novel pharmacological approaches for the treatment of these common conditions.