31
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Ghrelin and eating behavior: evidence and insights from genetically-modified mouse models

      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

          Ghrelin is an octanoylated peptide hormone, produced by endocrine cells of the stomach, which acts in the brain to increase food intake and body weight. Our understanding of the mechanisms underlying ghrelin's effects on eating behaviors has been greatly improved by the generation and study of several genetically manipulated mouse models. These models include mice overexpressing ghrelin and also mice with genetic deletion of ghrelin, the ghrelin receptor [the growth hormone secretagogue receptor (GHSR)] or the enzyme that post-translationally modifies ghrelin [ghrelin O-acyltransferase (GOAT)]. In addition, a GHSR-null mouse model in which GHSR transcription is globally blocked but can be cell-specifically reactivated in a Cre recombinase-mediated fashion has been generated. Here, we summarize findings obtained with these genetically manipulated mice, with the aim to highlight the significance of the ghrelin system in the regulation of both homeostatic and hedonic eating, including that occurring in the setting of chronic psychosocial stress.

          Related collections

          Most cited references80

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

            Agouti-related peptide-expressing neurons are mandatory for feeding.

            Multiple hormones controlling energy homeostasis regulate the expression of neuropeptide Y (NPY) and agouti-related peptide (AgRP) in the arcuate nucleus of the hypothalamus. Nevertheless, inactivation of the genes encoding NPY and/or AgRP has no impact on food intake in mice. Here we demonstrate that induced selective ablation of AgRP-expressing neurons in adult mice results in acute reduction of feeding, demonstrating direct evidence for a critical role of these neurons in the regulation of energy homeostasis.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Ghrelin octanoylation mediated by an orphan lipid transferase.

              The peptide hormone ghrelin is the only known protein modified with an O-linked octanoyl side group, which occurs on its third serine residue. This modification is crucial for ghrelin's physiological effects including regulation of feeding, adiposity, and insulin secretion. Despite the crucial role for octanoylation in the physiology of ghrelin, the lipid transferase that mediates this novel modification has remained unknown. Here we report the identification and characterization of human GOAT, the ghrelin O-acyl transferase. GOAT is a conserved orphan membrane-bound O-acyl transferase (MBOAT) that specifically octanoylates serine-3 of the ghrelin peptide. Transcripts for both GOAT and ghrelin occur predominantly in stomach and pancreas. GOAT is conserved across vertebrates, and genetic disruption of the GOAT gene in mice leads to complete absence of acylated ghrelin in circulation. The occurrence of ghrelin and GOAT in stomach and pancreas tissues demonstrates the relevance of GOAT in the acylation of ghrelin and further implicates acylated ghrelin in pancreatic function.
                Bookmark

                Author and article information

                Journal
                Front Neurosci
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                15 May 2013
                16 July 2013
                2013
                : 7
                : 121
                Affiliations
                [1] 1Divisions of Hypothalamic Research and Endocrinology and Metabolism, Department of Medicine, The University of Texas Southwestern Medical Center Dallas, TX, USA
                [2] 2Department of Psychiatry, The University of Texas Southwestern Medical Center Dallas, TX, USA
                [3] 3Laboratory of Neurophysiology of the Multidisciplinary Institute of Cell Biology [Argentine Research Council (CONICET) and Scientific Research Commission, Province of Buenos Aires (CIC-PBA)] La Plata, Buenos Aires, Argentina
                Author notes

                Edited by: Alfonso Abizaid, Carleton University, Canada

                Reviewed by: Julie A. Chowen, Hospital Infantil Universitario Niño Jesús, Spain; Stephanie Borgland, University of British Columbia, Canada

                *Correspondence: Jeffrey M. Zigman, Department of Medicine, The University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, MC 9077, Dallas, TX 75390-9077, USA e-mail: jeffrey.zigman@ 123456utsouthwestern.edu
                Mario Perelló, Laboratory of Neurophysiology of the Multidisciplinary Institute of Cell Biology [Argentine Research Council (CONICET) and Scientific Research Commission, Province of Buenos Aires (CIC-PBA)], Calle 526 S/N entre 10 y 11-PO Box 403, La Plata, Buenos Aires 1900, Argentina e-mail: marioperello@ 123456yahoo.com

                This article was submitted to Frontiers in Neuroendocrine Science, a specialty of Frontiers in Neuroscience.

                †These authors have contributed equally to this work.

                Article
                10.3389/fnins.2013.00121
                3712270
                23882175
                b5c7d4a7-6c34-4b42-a5e9-895ed91b9e14
                Copyright © 2013 Uchida, Zigman and Perelló.

                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
                : 29 April 2013
                : 25 June 2013
                Page count
                Figures: 0, Tables: 2, Equations: 0, References: 93, Pages: 10, Words: 9336
                Categories
                Endocrinology
                Review Article

                Neurosciences
                hedonic eating,homeostatic eating,goat,ghsr
                Neurosciences
                hedonic eating, homeostatic eating, goat, ghsr

                Comments

                Comment on this article