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      A mu–delta opioid receptor brain atlas reveals neuronal co-occurrence in subcortical networks

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          Abstract

          Opioid receptors are G protein-coupled receptors (GPCRs) that modulate brain function at all levels of neural integration, including autonomic, sensory, emotional and cognitive processing. Mu (MOR) and delta (DOR) opioid receptors functionally interact in vivo, but whether interactions occur at circuitry, cellular or molecular levels remains unsolved. To challenge the hypothesis of MOR/DOR heteromerization in the brain, we generated redMOR/greenDOR double knock-in mice and report dual receptor mapping throughout the nervous system. Data are organized as an interactive database offering an opioid receptor atlas with concomitant MOR/DOR visualization at subcellular resolution, accessible online. We also provide co-immunoprecipitation-based evidence for receptor heteromerization in these mice. In the forebrain, MOR and DOR are mainly detected in separate neurons, suggesting system-level interactions in high-order processing. In contrast, neuronal co-localization is detected in subcortical networks essential for survival involved in eating and sexual behaviors or perception and response to aversive stimuli. In addition, potential MOR/DOR intracellular interactions within the nociceptive pathway offer novel therapeutic perspectives.

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          The online version of this article (doi:10.1007/s00429-014-0717-9) contains supplementary material, which is available to authorized users.

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          Most cited references60

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          Cortical processing of odor objects.

          Natural odors, generally composed of many monomolecular components, are analyzed by peripheral receptors into component features and translated into spatiotemporal patterns of neural activity in the olfactory bulb. Here, we will discuss the role of the olfactory cortex in the recognition, separation and completion of those odor-evoked patterns, and how these processes contribute to odor perception. Recent findings regarding the neural architecture, physiology, and plasticity of the olfactory cortex, principally the piriform cortex, will be described in the context of how this paleocortical structure creates odor objects. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Balance disorders in the elderly.

            Good balance is an imperative skill for daily life that requires the complex integration of sensory information regarding the position of the body relative to the surroundings and the ability to generate appropriate motor responses to control body movement. Balance calls upon contributions from vision, vestibular sense, proprioception, muscle strength and reaction time. With increased age, there is a progressive loss of functioning of these systems which can contribute to balance deficits. Balance disorders represent a growing public health concern due to the association with falls and fall-related injuries, particularly in regions of the world in which high proportions of the population are elderly. Falls present one of the most serious and costly problems associated with older adulthood. Falls can mark the beginning of a decline in function and independence and are the leading cause of injury-related hospitalisation in older people. One in three people over the age of 65 years who are living in the community experience at least one fall each year and 10-15% of these falls are associated with serious injury. In economic terms, the direct and indirect costs associated with falls are large and will grow as the proportion of older people increases. Consequently, understanding age-related changes in the physiological systems imperative to balance is of utmost importance to prevent falls in older people and reduce the injury-related burden on individuals and society.
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              G-protein-coupled receptor heterodimerization modulates receptor function.

              The opioid system modulates several physiological processes, including analgesia, the stress response, the immune response and neuroendocrine function. Pharmacological and molecular cloning studies have identified three opioid-receptor types, delta, kappa and mu, that mediate these diverse effects. Little is known about the ability of the receptors to interact to form new functional structures, the simplest of which would be a dimer. Structural and biochemical studies show that other G-protein-coupled receptors (GPCRs) interact to form homodimers. Moreover, two non-functional receptors heterodimerize to form a functional receptor, suggesting that dimerization is crucial for receptor function. However, heterodimerization between two fully functional receptors has not been documented. Here we provide biochemical and pharmacological evidence for the heterodimerization of two fully functional opioid receptors, kappa and delta. This results in a new receptor that exhibits ligand binding and functional properties that are distinct from those of either receptor. Furthermore, the kappa-delta heterodimer synergistically binds highly selective agonists and potentiates signal transduction. Thus, heterodimerization of these GPCRs represents a novel mechanism that modulates their function.
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                Author and article information

                Contributors
                briki@igbmc.fr
                d.massotte@unistra.fr
                Journal
                Brain Struct Funct
                Brain Struct Funct
                Brain Structure & Function
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                1863-2653
                1863-2661
                13 March 2014
                13 March 2014
                2015
                : 220
                : 2
                : 677-702
                Affiliations
                [ ]Department of Neurogenetics and Translational Medicine, Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, INSERM, Université de Strasbourg, 1 rue Laurent Fries, BP10142, 67404 Illkirch cedex, France
                [ ]Department of Anesthesiology, Perioperative and Pain Medicine, Stanford Institute for Neuro-Innovation and Translational Neurosciences, Stanford University, Stanford, 94305 CA USA
                [ ]Imaging Centre, Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, INSERM, Université de Strasbourg, BP 10142, 1 rue Laurent Fries, 67404 Illkirch cedex, France
                [ ]Institut Clinique de la Souris, 1 rue Laurent Fries, 67404 Illkirch cedex, France
                [ ]Institut des Neurosciences Cellulaires et Intégratives CNRS UPR 3212, 5 rue Blaise Pascal, 67084 Strasbourg cedex 03, France
                [ ]University of California, La Jolla, CA 92093 USA
                [ ]Sanger Institute, Hinxton, Cambridge CB 10 1SA UK
                Article
                717
                10.1007/s00429-014-0717-9
                4341027
                24623156
                485901f3-f06f-46b6-aa69-435f6a171995
                © The Author(s) 2014

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

                History
                : 6 October 2013
                : 27 January 2014
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag Berlin Heidelberg 2015

                Neurology
                mouse mu opioid receptor,mouse delta opioid receptor,receptor brain atlas,heteromer,aversive stimuli

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