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Neurosteroids promote phosphorylation and membrane insertion of extrasynaptic GABAA receptors.


ABSTRACT: Neurosteroids are synthesized within the brain and act as endogenous anxiolytic, anticonvulsant, hypnotic, and sedative agents, actions that are principally mediated via their ability to potentiate phasic and tonic inhibitory neurotransmission mediated by ?-aminobutyric acid type A receptors (GABAARs). Although neurosteroids are accepted allosteric modulators of GABAARs, here we reveal they exert sustained effects on GABAergic inhibition by selectively enhancing the trafficking of GABAARs that mediate tonic inhibition. We demonstrate that neurosteroids potentiate the protein kinase C-dependent phosphorylation of S443 within ?4 subunits, a component of GABAAR subtypes that mediate tonic inhibition in many brain regions. This process enhances insertion of ?4 subunit-containing GABAAR subtypes into the membrane, resulting in a selective and sustained elevation in the efficacy of tonic inhibition. Therefore, the ability of neurosteroids to modulate the phosphorylation and membrane insertion of ?4 subunit-containing GABAARs may underlie the profound effects these endogenous signaling molecules have on neuronal excitability and behavior.

SUBMITTER: Abramian AM 

PROVIDER: S-EPMC4024867 | biostudies-other | 2014 May

REPOSITORIES: biostudies-other

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Neurosteroids promote phosphorylation and membrane insertion of extrasynaptic GABAA receptors.

Abramian Armen M AM   Comenencia-Ortiz Eydith E   Modgil Amit A   Vien Thuy N TN   Nakamura Yasuko Y   Moore Yvonne E YE   Maguire Jamie L JL   Terunuma Miho M   Davies Paul A PA   Moss Stephen J SJ  

Proceedings of the National Academy of Sciences of the United States of America 20140428 19


Neurosteroids are synthesized within the brain and act as endogenous anxiolytic, anticonvulsant, hypnotic, and sedative agents, actions that are principally mediated via their ability to potentiate phasic and tonic inhibitory neurotransmission mediated by γ-aminobutyric acid type A receptors (GABAARs). Although neurosteroids are accepted allosteric modulators of GABAARs, here we reveal they exert sustained effects on GABAergic inhibition by selectively enhancing the trafficking of GABAARs that m  ...[more]

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