10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The Role of Ghrelin in Regulating Synaptic Function and Plasticity of Feeding-Associated Circuits

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Synaptic plasticity of the neuronal circuits associated with feeding behavior is regulated by peripheral signals as a response to changes in the energy status of the body. These signals include glucose, free fatty acids, leptin and ghrelin and are released into circulation, being able to reach the brain. Ghrelin, a small peptide released from the stomach, is an orexigenic hormone produced in peripheral organs, and its action regulates food intake, body weight and glucose homeostasis. Behavioral studies show that ghrelin is implicated in the regulation of both hedonic and homeostatic feeding and of cognition. Ghrelin-induced synaptic plasticity has been described in neuronal circuits associated with these behaviors. In this review, we discuss the neuromodulatory mechanisms induced by ghrelin in regulating synaptic plasticity in three main neuronal circuits previously associated with feeding behaviors, namely hypothalamic (homeostatic feeding), ventral tegmental (hedonic and motivational feeding) and hippocampal (cognitive) circuits. Given the central role of ghrelin in regulating feeding behaviors, and the altered ghrelin levels associated with metabolic disorders such as obesity and anorexia, it is of paramount relevance to understand the effects of ghrelin on synaptic plasticity of neuronal circuits associated with feeding behaviors.

          Related collections

          Most cited references92

          • Record: found
          • Abstract: found
          • Article: not found

          Synaptic plasticity: multiple forms, functions, and mechanisms.

          Experiences, whether they be learning in a classroom, a stressful event, or ingestion of a psychoactive substance, impact the brain by modifying the activity and organization of specific neural circuitry. A major mechanism by which the neural activity generated by an experience modifies brain function is via modifications of synaptic transmission; that is, synaptic plasticity. Here, we review current understanding of the mechanisms of the major forms of synaptic plasticity at excitatory synapses in the mammalian brain. We also provide examples of the possible developmental and behavioral functions of synaptic plasticity and how maladaptive synaptic plasticity may contribute to neuropsychiatric disorders.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Drug-evoked synaptic plasticity in addiction: from molecular changes to circuit remodeling.

            Addictive drugs have in common that they target the mesocorticolimbic dopamine (DA) system. This system originates in the ventral tegmental area (VTA) and projects mainly to the nucleus accumbens (NAc) and prefrontal cortex (PFC). Here, we review the effects that such drugs leave on glutamatergic and GABAergic synaptic transmission in these three brain areas. We refer to these changes as drug-evoked synaptic plasticity, which outlasts the presence of the drug in the brain and contributes to the reorganization of neural circuits. While in most cases these early changes are not sufficient to induce the disease, with repetitive drug exposure, they may add up and contribute to addictive behavior. Copyright © 2011 Elsevier Inc. All rights reserved.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              A receptor in pituitary and hypothalamus that functions in growth hormone release.

              Small synthetic molecules termed growth hormone secretagogues (GHSs) act on the pituitary gland and the hypothalamus to stimulate and amplify pulsatile growth hormone (GH) release. A heterotrimeric GTP-binding protein (G protein)-coupled receptor (GPC-R) of the pituitary and arcuate ventro-medial and infundibular hypothalamus of swine and humans was cloned and was shown to be the target of the GHSs. On the basis of its pharmacological and molecular characterization, this GPC-R defines a neuroendocrine pathway for the control of pulsatile GH release and supports the notion that the GHSs mimic an undiscovered hormone.
                Bookmark

                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
                27 May 2019
                2019
                : 13
                : 205
                Affiliations
                [1] 1Center for Neuroscience and Cell Biology (CNC), University of Coimbra , Coimbra, Portugal
                [2] 2Institute for Interdisciplinary Research (IIIUC), University of Coimbra , Coimbra, Portugal
                [3] 3PhD Program in Experimental Biology and Biomedicine (PDBEB), University of Coimbra , Coimbra, Portugal
                [4] 4Department of Life Sciences, University of Coimbra , Coimbra, Portugal
                Author notes

                Edited by: Margherita Maffei, Italian National Research Council (CNR), Italy

                Reviewed by: Mario Perello, National Scientific and Technical Research Council (CONICET), Argentina; Omar Al Massadi, Sorbonne Universités, France

                *Correspondence: Ana Luísa Carvalho, alc@ 123456cnc.uc.pt

                This article was submitted to Cellular Neurophysiology, a section of the journal Frontiers in Cellular Neuroscience

                Article
                10.3389/fncel.2019.00205
                6546032
                31191250
                51130408-677d-4b45-8e82-3c64184f4b7a
                Copyright © 2019 Serrenho, Santos and Carvalho.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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
                : 05 January 2019
                : 24 April 2019
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 117, Pages: 13, Words: 0
                Funding
                Funded by: Fundação para a Ciência e a Tecnologia 10.13039/501100001871
                Award ID: POCI-01-0145-FEDER-028541
                Award ID: POCI-01-0145-029452
                Funded by: European Regional Development Fund 10.13039/501100008530
                Categories
                Neuroscience
                Review

                Neurosciences
                ghrelin,synaptic plasticity,hypothalamus,ventral tegmental area,hippocampus,feeding
                Neurosciences
                ghrelin, synaptic plasticity, hypothalamus, ventral tegmental area, hippocampus, feeding

                Comments

                Comment on this article