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44361 - PROBING THE IDENTITY OF GABAA RECEPTORS THAT UNDERLIE AMNESTIC PROPERTIES OF ANESTHETICS

¹ Sunnybrook Health Sciences Centre, Toronto, ON, Canada
² Hospital for Sick Children
³ Hospital for Sick Children and University of Toronto
⁴ University of Toronto

Abstract

INTRODUCTION: The desirable components of the anesthetic state include amnesia, hypnosis, immobility and analgesia. Different anatomical regions and receptors are thought to mediate these distinct behavioral end-points. In order to design specific drugs, it is essential to know the protein structure of anesthetic targets. Our aim is to identify specific receptors that underlie the amnestic properties of anesthetics. GABAA receptors which mediate most inhibitory neurotransmission are targets for injectable and inhaled anesthetics. GABAA receptors are pentameric complexes that are composed of multiple subunits (α1–6, β1–3, γ1–4, δ, ρ1–3, σ, π) which determine physiologic properties and sensitivities to anesthetics (1,2). In particular, GABAA receptors that contain the α5 subunit play a critical role in learning and memory (3,4). Genetic deletion of the α5 subunit conferred resistance to the amnestic properties of the anesthetic etomidate in a mouse model, whereas sedation and hypnosis remained intact (5). The goal of this study was to identify the subunits that combine with the α5 subunit to form functional GABAA receptors in hippocampal neurons.

METHODS: Studies were approved by the local Animal Care Committee. C57/BL6 mouse hippocampi were isolated and fractionated to enrich for synaptosomal and nonsynaptosomal protein complexes. Immunoprecipitation was performed using a polyclonal antibody raised against the major intracytoplasmic loop of the GABAA receptor α5 subunit (Sigma, Saint Louis, MO). The complexes were fractionated by size using SDS-gel electrophoresis and purified. After trypsin digestion, proteins were identified using mass spectrometry.

RESULTS: Mass spectrometry showed that α5 subunit associates with not one α or β isoform, but rather with a diverse number of subunits including α1, α2, β1, β3 and γ2.

DISCUSSION: The results provide the first direct evidence that GABAA receptors that contain the α5 subunit represent a heterogenous population which incorporate several α and β isoforms. Since current models suggest that individual GABAA receptor isoforms mediate the specificity of GABA’s physiological effects, the results predict that α5 GABAA containing receptors will exhibit diversity in their trafficking (6), pharmacology and physiological properties (1,2). The results change our basic understanding of these receptors and will modify our approach to future drug design.

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