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Publication : Tonic inhibition in principal cells of the amygdala: a central role for α3 subunit-containing GABAA receptors.

First Author  Marowsky A Year  2012
Journal  J Neurosci Volume  32
Issue  25 Pages  8611-9
PubMed ID  22723702 Mgi Jnum  J:185661
Mgi Id  MGI:5429633 Doi  10.1523/JNEUROSCI.4404-11.2012
Citation  Marowsky A, et al. (2012) Tonic Inhibition in Principal Cells of the Amygdala: A Central Role for alpha3 Subunit-Containing GABAA Receptors. J Neurosci 32(25):8611-9
abstractText  GABAergic inhibition in the amygdala is essential in regulating fear and anxiety. Although fast "phasic" inhibition arising through the activation of postsynaptic GABA(A) receptors (GABA(A)Rs) has been well described in the amygdala, much less is known about extrasynaptic GABA(A)Rs mediating persistent or tonic inhibition and regulating neuronal excitability. Here, we recorded tonic currents in the basolateral (BLA) nucleus and the lateral (LA) nucleus of the amygdala. While all BLA principal cells expressed a robust GABAergic tonic current, only 70% of LA principal cells showed a tonic current. Immunohistochemical stainings revealed that the alpha3 GABA(A)R subunit is expressed moderately in the LA and strongly throughout the BLA nucleus, where it is located mostly at extrasynaptic sites. In alpha3 subunit KO mice, tonic currents are significantly reduced in BLA principal cells yet not in LA principal cells. Moreover, the alpha3 GABA(A)R-selective benzodiazepine site agonist and anxiolytic compound TP003 increases tonic currents and dampens excitability markedly in wild-type BLA principal cells but fails to do so in alpha3KO BLA cells. Interneurons of the LA and BLA nuclei also express a tonic current, but TP003-induced potentiation is seen in only a small fraction of these cells, suggesting that primarily other GABA(A)R variants underlie tonic inhibition in this cell type. Together, these studies demonstrate that alpha3 GABA(A)R-mediated tonic inhibition is a central component of the inhibitory force in the amygdala and that tonically activated alpha3 GABA(A)Rs present an important target for anxiolytic or fear-reducing compounds.
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