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      Potentiation of Gamma Aminobutyric Acid Receptors (GABA AR) by Ethanol: How Are Inhibitory Receptors Affected?

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          Abstract

          In recent years there has been an increase in the understanding of ethanol actions on the type A γ-aminobutyric acid chloride channel (GABA AR), a member of the pentameric ligand gated ion channels (pLGICs). However, the mechanism by which ethanol potentiates the complex is still not fully understood and a number of publications have shown contradictory results. Thus many questions still remain unresolved requiring further studies for a better comprehension of this effect. The present review concentrates on the involvement of GABA AR in the acute actions of ethanol and specifically focuses on the immediate, direct or indirect, synaptic and extra-synaptic modulatory effects. To elaborate on the immediate, direct modulation of GABA AR by acute ethanol exposure, electrophysiological studies investigating the importance of different subunits, and data from receptor mutants will be examined. We will also discuss the nature of the putative binding sites for ethanol based on structural data obtained from other members of the pLGICs family. Finally, we will briefly highlight the glycine gated chloride channel (GlyR), another member of the pLGIC family, as a suitable target for the development of new pharmacological tools.

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          Genetics of mouse behavior: interactions with laboratory environment.

          Strains of mice that show characteristic patterns of behavior are critical for research in neurobehavioral genetics. Possible confounding influences of the laboratory environment were studied in several inbred strains and one null mutant by simultaneous testing in three laboratories on a battery of six behaviors. Apparatus, test protocols, and many environmental variables were rigorously equated. Strains differed markedly in all behaviors, and despite standardization, there were systematic differences in behavior across labs. For some tests, the magnitude of genetic differences depended upon the specific testing lab. Thus, experiments characterizing mutants may yield results that are idiosyncratic to a particular laboratory.
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            Crystal structure of a human GABAA receptor

            Summary Type-A γ-aminobutyric acid receptors (GABAARs) are the principal mediators of rapid inhibitory synaptic transmission in the human brain. A decline in GABAAR signalling triggers hyperactive neurological disorders such as insomnia, anxiety and epilepsy. Here we present the first three-dimensional structure of a GABAAR, the human β3 homopentamer, at 3 Å resolution. This structure reveals architectural elements unique to eukaryotic Cys-loop receptors, explains the mechanistic consequences of multiple human disease mutations and shows a surprising structural role for a conserved N-linked glycan. The receptor was crystallised bound to a previously unknown agonist, benzamidine, opening a new avenue for the rational design of GABAAR modulators. The channel region forms a closed gate at the base of the pore, representative of a desensitised state. These results offer new insights into the signalling mechanisms of pentameric ligand-gated ion channels and enhance current understanding of GABAergic neurotransmission.
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              GABA(A) receptor trafficking and its role in the dynamic modulation of neuronal inhibition.

              GABA (gamma-aminobutyric acid) type A receptors (GABA(A)Rs) mediate most fast synaptic inhibition in the mammalian brain, controlling activity at both the network and the cellular levels. The diverse functions of GABA in the CNS are matched not just by the heterogeneity of GABA(A)Rs, but also by the complex trafficking mechanisms and protein-protein interactions that generate and maintain an appropriate receptor cell-surface localization. In this Review, we discuss recent progress in our understanding of the dynamic regulation of GABA(A)R composition, trafficking to and from the neuronal surface, and lateral movement of receptors between synaptic and extrasynaptic locations. Finally, we highlight a number of neurological disorders, including epilepsy and schizophrenia, in which alterations in GABA(A)R trafficking occur.
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                Author and article information

                Contributors
                Journal
                Front Cell Neurosci
                Front Cell Neurosci
                Front. Cell. Neurosci.
                Frontiers in Cellular Neuroscience
                Frontiers Media S.A.
                1662-5102
                06 May 2016
                2016
                : 10
                : 114
                Affiliations
                [1] 1Laboratory of Neurophysiology, Department of Physiology, University of Concepcion Concepcion, Chile
                [2] 2Laboratory of Environmental Neurotoxicology, Department of Biomedical Sciences, Faculty of Medicine, Universidad Católica del Norte Coquimbo, Chile
                [3] 3Hindbrain Integrative Neurobiology Laboratory, Institut de Neurobiologie Alfred Fessard Gif-Sur-Yvette, France
                Author notes

                Edited by: Egidio D‘Angelo, University of Pavia, Italy

                Reviewed by: Wen-Jun Gao, Drexel University College of Medicine, USA; Yuriko Iwakura, Niigata University, Japan

                *Correspondence: Luis G. Aguayo luisagua@ 123456gmail.com
                Article
                10.3389/fncel.2016.00114
                4858537
                27199667
                c9eb433d-1b9e-4717-82b2-c2a929ac329c
                Copyright © 2016 Förstera, Castro, Moraga-Cid and Aguayo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 25 January 2016
                : 20 April 2016
                Page count
                Figures: 2, Tables: 3, Equations: 0, References: 206, Pages: 17, Words: 16191
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: R01AA15150
                Funded by: Comisión Nacional de Investigación Científica y Tecnológica 10.13039/501100002848
                Award ID: DPI 20140008
                Funded by: Fondo Nacional de Desarrollo Científico y Tecnológico 10.13039/501100002850
                Award ID: Postdoctorado 2014 Grant number 3140194
                Categories
                Neuroscience
                Review

                Neurosciences
                alcoholism,ethanol,gaba,gabaar,glyr
                Neurosciences
                alcoholism, ethanol, gaba, gabaar, glyr

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