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Estrous Cycle Regulation of Extrasynaptic δ-Containing GABAA Receptor-Mediated Tonic Inhibition and Limbic Epileptogenesis
- Publication Year :
- 2013
- Publisher :
- The American Society for Pharmacology and Experimental Therapeutics, 2013.
-
Abstract
- The ovarian cycle affects susceptibility to behavioral and neurologic conditions. The molecular mechanisms underlying these changes are poorly understood. Deficits in cyclical fluctuations in steroid hormones and receptor plasticity play a central role in physiologic and pathophysiologic menstrual conditions. It has been suggested that synaptic GABA(A) receptors mediate phasic inhibition in the hippocampus and extrasynaptic receptors mediate tonic inhibition in the dentate gyrus. Here we report a novel role of extrasynaptic δ-containing GABA(A) receptors as crucial mediators of the estrous cycle-related changes in neuronal excitability in mice, with hippocampus subfield specificity. In molecular and immunofluorescence studies, a significant increase occurred in δ-subunit, but not α4- and γ2-subunits, in the dentate gyrus during diestrus. However, δ-subunit upregulation was not evident in the CA1 region. The δ-subunit expression was undiminished by age and ovariectomy and in mice lacking progesterone receptors, but it was significantly reduced by finasteride, a neurosteroid synthesis inhibitor. Electrophysiologic studies confirmed greater potentiation of GABA currents by progesterone-derived neurosteroid allopregnanolone in dissociated dentate gyrus granule cells in diestrus than in CA1 pyramidal cells. The baseline conductance and allopregnanolone potentiation of tonic currents in dentate granule cells from hippocampal slices were higher than in CA1 pyramidal cells. In behavioral studies, susceptibility to hippocampus kindling epileptogenesis was lower in mice during diestrus. These results demonstrate the estrous cycle-related plasticity of neurosteroid-sensitive, δ-containing GABA(A) receptors that mediate tonic inhibition and seizure susceptibility. These findings may provide novel insight on molecular cascades of menstrual disorders like catamenial epilepsy, premenstrual syndrome, and migraine.
- Subjects :
- medicine.medical_specialty
Neuroactive steroid
Estrous Cycle
Nerve Tissue Proteins
Pregnanolone
Biology
Hippocampal formation
In Vitro Techniques
Epileptogenesis
chemistry.chemical_compound
Mice
Neuropharmacology
5-alpha Reductase Inhibitors
Internal medicine
medicine
Catamenial epilepsy
Kindling, Neurologic
Animals
GABAergic Neurons
CA1 Region, Hippocampal
Progesterone
Pharmacology
Mice, Knockout
Epilepsy
Neuronal Plasticity
Behavior, Animal
GABAA receptor
Dentate gyrus
Allopregnanolone
Long-term potentiation
Neural Inhibition
Receptors, GABA-A
Protein Subunits
Endocrinology
chemistry
nervous system
Gene Expression Regulation
Dentate Gyrus
Molecular Medicine
Female
Disease Susceptibility
Receptors, Progesterone
Neuroscience
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....30a623d1aded4c745d9f9e7cf1146739