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      Cholinergic connectivity: it's implications for psychiatric disorders

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          Abstract

          Acetylcholine has been implicated in both the pathophysiology and treatment of a number of psychiatric disorders, with most of the data related to its role and therapeutic potential focusing on schizophrenia. However, there is little thought given to the consequences of the documented changes in the cholinergic system and how they may affect the functioning of the brain. This review looks at the cholinergic system and its interactions with the intrinsic neurotransmitters glutamate and gamma-amino butyric acid as well as those with the projection neurotransmitters most implicated in the pathophysiologies of psychiatric disorders; dopamine and serotonin. In addition, with the recent focus on the role of factors normally associated with inflammation in the pathophysiologies of psychiatric disorders, links between the cholinergic system and these factors will also be examined. These interfaces are put into context, primarily for schizophrenia, by looking at the changes in each of these systems in the disorder and exploring, theoretically, whether the changes are interconnected with those seen in the cholinergic system. Thus, this review will provide a comprehensive overview of the connectivity between the cholinergic system and some of the major areas of research into the pathophysiologies of psychiatric disorders, resulting in a critical appraisal of the potential outcomes of a dysregulated central cholinergic system.

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          Most cited references336

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          The basal ganglia are a chain of subcortical nuclei that facilitate action selection. Two striatal projection systems--so-called direct and indirect pathways--form the functional backbone of the basal ganglia circuit. Twenty years ago, investigators proposed that the striatum's ability to use dopamine (DA) rise and fall to control action selection was due to the segregation of D(1) and D(2) DA receptors in direct- and indirect-pathway spiny projection neurons. Although this hypothesis sparked a debate, the evidence that has accumulated since then clearly supports this model. Recent advances in the means of marking neural circuits with optical or molecular reporters have revealed a clear-cut dichotomy between these two cell types at the molecular, anatomical, and physiological levels. The contrast provided by these studies has provided new insights into how the striatum responds to fluctuations in DA signaling and how diseases that alter this signaling change striatal function.
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            The metabotropic glutamate receptors (mGluRs) are family C G-protein-coupled receptors that participate in the modulation of synaptic transmission and neuronal excitability throughout the central nervous system. The mGluRs bind glutamate within a large extracellular domain and transmit signals through the receptor protein to intracellular signaling partners. A great deal of progress has been made in determining the mechanisms by which mGluRs are activated, proteins with which they interact, and orthosteric and allosteric ligands that can modulate receptor activity. The widespread expression of mGluRs makes these receptors particularly attractive drug targets, and recent studies continue to validate the therapeutic utility of mGluR ligands in neurological and psychiatric disorders such as Alzheimer's disease, Parkinson's disease, anxiety, depression, and schizophrenia.
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                Author and article information

                Journal
                Front Cell Neurosci
                Front Cell Neurosci
                Front. Cell. Neurosci.
                Frontiers in Cellular Neuroscience
                Frontiers Media S.A.
                1662-5102
                03 May 2013
                2013
                : 7
                : 55
                Affiliations
                [1] 1Department of Psychiatry, The University of Melbourne Parkville, VIC, Australia
                [2] 2Molecular Psychiatry Laboratories, Florey Institute of Neuroscience and Mental Health Parkville, VIC, Australia
                [3] 3Centre for Neuroscience, The University of Melbourne Parkville, VIC, Australia
                Author notes

                Edited by: Chao Deng, University of Wollongong, Australia

                Reviewed by: Hermona Soreq, The Hebrew University of Jerusalem, Israel; Katerina Zavitsanou, University New South Wales, Australia

                *Correspondence: Elizabeth Scarr, Department of Psychiatry, Melbourne Brain Centre, The University of Melbourne, Kenneth Myer Building, Melbourne, VIC 3010, Australia. e-mail: elscarr@ 123456unimelb.edu.au
                Article
                10.3389/fncel.2013.00055
                3642390
                23653591
                61779114-5e2c-4e0d-96be-de2c0a30621b
                Copyright © 2013 Scarr, Gibbons, Neo, Udawela and Dean.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 02 January 2013
                : 12 April 2013
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 372, Pages: 26, Words: 24784
                Categories
                Neuroscience
                Review Article

                Neurosciences
                acetylcholine,psychiatric disorders,glutamate,gaba,dopamine,serotonin,cytokines
                Neurosciences
                acetylcholine, psychiatric disorders, glutamate, gaba, dopamine, serotonin, cytokines

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