Extrasynaptic GABAA Receptors and Tonic Inhibition in Rat Auditory Thalamus
Background Neural inhibition plays an important role in auditory processing and attentional gating. Extrasynaptic GABAA receptors (GABAAR), containing α4and δ GABAAR subunits, are thought to be activated by GABA spillover outside of the synapse following release resulting in a tonic inhibitory Cl− c...
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Published in | PloS one Vol. 6; no. 1; p. e16508 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
San Francisco
Public Library of Science
2011
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Subjects | |
Online Access | Get full text |
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Summary: | Background Neural inhibition plays an important role in auditory processing and attentional gating. Extrasynaptic GABAA receptors (GABAAR), containing α4and δ GABAAR subunits, are thought to be activated by GABA spillover outside of the synapse following release resulting in a tonic inhibitory Cl− current which could account for up to 90% of total inhibition in visual and somatosensory thalamus. However, the presence of this unique type of inhibition has not been identified in auditory thalamus. Methodology/Principal Findings The present study used gaboxadol, a partially selective potent agonist for δ-subunit containing GABAA receptor constructs to elucidate the presence of extrasynaptic GABAARs using both a quantitative receptor binding assay and patch-clamp electrophysiology in thalamic brain slices. Intense [3H]gaboxadol binding was found to be localized to the MGB while whole cell recordings from MGB neurons in the presence of gaboxadol demonstrated the expression of δ-subunit containing GABAARs capable of mediating a tonic inhibitory Cl− current. Conclusions/Significance Potent tonic inhibitory GABAAR responses mediated by extrasynaptic receptors may be important in understanding how acoustic information is processed by auditory thalamic neurons as it ascends to auditory cortex. In addition to affecting cellular behavior and possibly neurotransmission, functional extrasynaptic δ-subunit containing GABAARs may represent a novel pharmacological target for the treatment of auditory pathologies including temporal processing disorders or tinnitus. |
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Bibliography: | Conceived and designed the experiments: BDR DMC LLL VVU. Performed the experiments: BDR LLL. Analyzed the data: BDR LLL VVU DMC. Contributed reagents/materials/analysis tools: BDR LLL VVU DMC. Wrote the paper: BDR DMC LLL VVU. Obtained [3H] Gaboxadol: DMC. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0016508 |