4.7 Article

A new naturally occurring GABA(A) receptor subunit partnership with high sensitivity to ethanol

Journal

NATURE NEUROSCIENCE
Volume 10, Issue 1, Pages 40-48

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nn1813

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Funding

  1. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS030549, R01NS051311, R37NS030549, R56NS051311] Funding Source: NIH RePORTER
  2. Veterans Affairs [I01BX000404] Funding Source: NIH RePORTER
  3. NIAAA NIH HHS [AA14003] Funding Source: Medline
  4. NINDS NIH HHS [NS051311, NS30549, NS35958] Funding Source: Medline
  5. BLRD VA [I01 BX000404] Funding Source: Medline

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According to the rules of GABA(A) receptor (GABA(A)R) subunit assembly, alpha 4 and alpha 6 subunits are considered to be the natural partners of delta subunits. These GABA(A)Rs are a preferred target of low, sobriety-impairing concentrations of ethanol. Here we demonstrate a new naturally occurring GABAAR subunit partnership: d subunits of hippocampal interneurons are coexpressed and colocalized with alpha 1 subunits, but not with alpha 4, alpha 6 or any other alpha subunits. Ethanol potentiates the tonic inhibition mediated by such native alpha 1/delta GABA(A)Rs in wild-type and in alpha 4 subunit-deficient (Gabra4(-/-)) mice, but not in delta subunit - deficient (Gabrd(-/-)) mice. We also ruled out any compensatory upregulation of alpha 6 subunits that might have accounted for the ethanol effect in Gabra4(-/-) mice. Thus, alpha 1/delta subunit assemblies represent a new neuronal GABA(A)R subunit partnership present in hippocampal interneurons, mediate tonic inhibitory currents and are highly sensitive to low concentrations of ethanol.

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