PT  - JOURNAL ARTICLE
AU  - Delia Belelli
AU  - Dianne R. Peden
AU  - Thomas W. Rosahl
AU  - Keith A. Wafford
AU  - Jeremy J. Lambert
TI  - Extrasynaptic GABA<sub>A</sub> Receptors of Thalamocortical Neurons: A Molecular Target for Hypnotics
AID  - 10.1523/JNEUROSCI.2679-05.2005
DP  - 2005 Dec 14
TA  - The Journal of Neuroscience
PG  - 11513--11520
VI  - 25
IP  - 50
4099  - http://www.jneurosci.org/content/25/50/11513.short
4100  - http://www.jneurosci.org/content/25/50/11513.full
SO  - J. Neurosci.2005 Dec 14; 25
AB  - Among hypnotic agents that enhance GABAA receptor function, etomidate is unusual because it is selective for β2/β3 compared with β1 subunit-containing GABAA receptors. Mice incorporating an etomidate-insensitive β2 subunit (β2N265S) revealed that β2 subunit-containing receptors mediate the enhancement of slow-wave activity (SWA) by etomidate, are required for the sedative, and contribute to the hypnotic actions of this anesthetic. Although the anatomical location of the β2-containing receptors that mediate these actions is unknown, the thalamus is implicated. We have characterized GABAA receptor-mediated neurotransmission in thalamic nucleus reticularis (nRT) and ventrobasalis complex (VB) neurons of wild-type, β–/–2, and β2N265S mice. VB but not nRT neurons exhibit a large GABA-mediated tonic conductance that contributes ∼80% of the total GABAA receptor-mediated transmission. Consequently, although etomidate enhances inhibition in both neuronal types, the effect of this anesthetic on the tonic conductance of VB neurons is dominant. The GABA-enhancing actions of etomidate in VB but not nRT neurons are greatly suppressed by the β2N265S mutation. The hypnotic THIP (Gaboxadol) induces SWA and at low, clinically relevant concentrations (30 nm to 3 μm) increases the tonic conductance of VB neurons, with no effect on VB or nRT miniature IPSCs (mIPSCs) or on the holding current of nRT neurons. Zolpidem, which has no effect on SWA, prolongs VB mIPSCs but is ineffective on the phasic and tonic conductance of nRT and VB neurons, respectively. Collectively, these findings suggest that enhancement of extrasynaptic inhibition in the thalamus may contribute to the distinct sleep EEG profiles of etomidate and THIP compared with zolpidem.