Literature DB >> 28536106

α2 Subunit-Containing GABAA Receptor Subtypes Are Upregulated and Contribute to Alcohol-Induced Functional Plasticity in the Rat Hippocampus.

A Kerstin Lindemeyer1, Yi Shen2, Ferin Yazdani2, Xuesi M Shao2, Igor Spigelman2, Daryl L Davies2, Richard W Olsen2, Jing Liang1.   

Abstract

Alcohol (EtOH) intoxication causes changes in the rodent brain γ-aminobutyric acid receptor (GABAAR) subunit composition and function, playing a crucial role in EtOH withdrawal symptoms and dependence. Building evidence indicates that withdrawal from acute EtOH and chronic intermittent EtOH (CIE) results in decreased EtOH-enhanced GABAAR δ subunit-containing extrasynaptic and EtOH-insensitive α1βγ2 subtype synaptic GABAARs but increased synaptic α4βγ2 subtype, and increased EtOH sensitivity of GABAAR miniature postsynaptic currents (mIPSCs) correlated with EtOH dependence. Here we demonstrate that after acute EtOH intoxication and CIE, upregulation of hippocampal α4βγ2 subtypes, as well as increased cell-surface levels of GABAAR α2 and γ1 subunits, along with increased α2β1γ1 GABAAR pentamers in hippocampal slices using cell-surface cross-linking, followed by Western blot and coimmunoprecipitation. One-dose and two-dose acute EtOH treatments produced temporal plastic changes in EtOH-induced anxiolysis or withdrawal anxiety, and the presence or absence of EtOH-sensitive synaptic currents correlated with cell surface peptide levels of both α4 and γ1(new α2) subunits. CIE increased the abundance of novel mIPSC patterns differing in activation/deactivation kinetics, charge transfer, and sensitivity to EtOH. The different mIPSC patterns in CIE could be correlated with upregulated highly EtOH-sensitive α2βγ subtypes and EtOH-sensitive α4βγ2 subtypes. Naïve α4 subunit knockout mice express EtOH-sensitive mIPSCs in hippocampal slices, correlating with upregulated GABAAR α2 (and not α4) subunits. Consistent with α2, β1, and γ1 subunits genetically linked to alcoholism in humans, our findings indicate that these new α2-containing synaptic GABAARs could mediate the maintained anxiolytic response to EtOH in dependent individuals, rat or human, contributing to elevated EtOH consumption.
Copyright © 2017 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2017        PMID: 28536106      PMCID: PMC5508196          DOI: 10.1124/mol.116.107797

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  72 in total

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2.  Bidirectional alterations of GABA(A) receptor subunit peptide levels in rat cortex during chronic ethanol consumption and withdrawal.

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5.  GABAA receptor alpha 4 subunits mediate extrasynaptic inhibition in thalamus and dentate gyrus and the action of gaboxadol.

Authors:  D Chandra; F Jia; J Liang; Z Peng; A Suryanarayanan; D F Werner; I Spigelman; C R Houser; R W Olsen; N L Harrison; G E Homanics
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8.  Functional comparison of the role of gamma subunits in recombinant human gamma-aminobutyric acidA/benzodiazepine receptors.

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9.  Plasticity of GABA(A) receptor-mediated neurotransmission in the nucleus accumbens of alcohol-dependent rats.

Authors:  Jing Liang; A Kerstin Lindemeyer; Asha Suryanarayanan; Edward M Meyer; Vincent N Marty; S Omar Ahmad; Xuesi Max Shao; Richard W Olsen; Igor Spigelman
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Authors:  Nianhui Zhang; Zechun Peng; Xiaoping Tong; A Kerstin Lindemeyer; Yliana Cetina; Christine S Huang; Richard W Olsen; Thomas S Otis; Carolyn R Houser
Journal:  Exp Neurol       Date:  2017-08-16       Impact factor: 5.330

3.  Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo.

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Journal:  Front Cell Neurosci       Date:  2018-01-31       Impact factor: 5.505

Review 4.  Role of GABAA receptors in alcohol use disorders suggested by chronic intermittent ethanol (CIE) rodent model.

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Review 5.  Regulation of GABAA Receptor Subunit Expression in Substance Use Disorders.

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7.  Nucleus accumbens shell small conductance potassium channels underlie adolescent ethanol exposure-induced anxiety.

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