AUTHOR=Modgil Amit , Vien Thuy N. , Ackley Michael A. , Doherty James J. , Moss Stephen J. , Davies Paul A. 

TITLE=Neuroactive Steroids Reverse Tonic Inhibitory Deficits in Fragile X Syndrome Mouse Model

JOURNAL=Frontiers in Molecular Neuroscience

VOLUME=12

YEAR=2019

URL=https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2019.00015

DOI=10.3389/fnmol.2019.00015

ISSN=1662-5099

ABSTRACT=<p>Fragile X syndrome (FXS) is the most common form of inherited intellectual disability. A reduction in neuronal inhibition mediated by γ-aminobutyric acid type A receptors (GABA<sub>A</sub>Rs) has been implicated in the pathophysiology of FXS. Neuroactive steroids (NASs) are known allosteric modulators of GABA<sub>A</sub>R channel function, but recent studies from our laboratory have revealed that NASs also exert persistent metabotropic effects on the efficacy of tonic inhibition by increasing the protein kinase C (PKC)-mediated phosphorylation of the α4 and β3 subunits which increase the membrane expression and boosts tonic inhibition. We have assessed the GABAergic signaling in the hippocampus of fragile X mental retardation protein (FMRP) knock-out (<italic>Fmr1</italic><italic>KO</italic>) mouse. The GABAergic tonic current in dentate gyrus granule cells (DGGCs) from 3- to 5-week-old (p21–35) <italic>Fmr1</italic><italic>KO</italic> mice was significantly reduced compared to WT mice. Additionally, spontaneous inhibitory post synaptic inhibitory current (sIPSC) amplitudes were increased in DGGCs from <italic>Fmr1 KO</italic> mice. While sIPSCs decay in both genotypes was prolonged by the prototypic benzodiazepine diazepam, those in <italic>Frm1-KO</italic> mice were selectively potentiated by RO15-4513. Consistent with this altered pharmacology, modifications in the expression levels and phosphorylation of receptor GABA<sub>A</sub>R subtypes that mediate tonic inhibition were seen in <italic>Fmr1 KO</italic> mice. Significantly, exposure to NASs induced a sustained elevation in tonic current in <italic>Fmr1 KO</italic> mice which was prevented with PKC inhibition. Likewise, exposure reduced elevated membrane excitability seen in the mutant mice. Collectively, our results suggest that NAS act to reverse the deficits of tonic inhibition seen in FXS, and thereby reduce aberrant neuronal hyperexcitability seen in this disorder.</p>