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The melanocortin-4 receptor is expressed in enteroendocrine L cells and regulates the release of peptide YY and glucagon-like peptide 1 in vivo.
Panaro, Brandon L; Tough, Iain R; Engelstoft, Maja S; Matthews, Robert T; Digby, Gregory J; Møller, Cathrine L; Svendsen, Berit; Gribble, Fiona; Reimann, Frank; Holst, Jens J; Holst, Birgitte; Schwartz, Thue W; Cox, Helen M; Cone, Roger D.
Afiliação
  • Panaro BL; Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
  • Tough IR; King's College London, Wolfson Centre for Age-Related Diseases, Guy's Campus, London SE1 1UL, UK.
  • Engelstoft MS; Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Receptology and Enteroendocrinology, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Denmark; Laboratory for Molecular Pharmacology, Department of Neuroscience and Pharmacology, Faculty of Medic
  • Matthews RT; Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
  • Digby GJ; Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
  • Møller CL; Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Receptology and Enteroendocrinology, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Denmark; Laboratory for Molecular Pharmacology, Department of Neuroscience and Pharmacology, Faculty of Medic
  • Svendsen B; Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Receptology and Enteroendocrinology, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Denmark; Department of Biomedical Sciences, Faculty of Health Sciences, University of Copenhagen, 2200 Denmar
  • Gribble F; University of Cambridge, Cambridge Institute for Medical Research (CIMR) & MRC Metabolic Diseases Unit (MDU), Addenbrooke's Hospital, Hills Road, Cambridge CB2 0XY, UK.
  • Reimann F; University of Cambridge, Cambridge Institute for Medical Research (CIMR) & MRC Metabolic Diseases Unit (MDU), Addenbrooke's Hospital, Hills Road, Cambridge CB2 0XY, UK.
  • Holst JJ; Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Receptology and Enteroendocrinology, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Denmark; Danish Diabetes Academy, 5000 Odense, Denmark.
  • Holst B; Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Receptology and Enteroendocrinology, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Denmark; Laboratory for Molecular Pharmacology, Department of Neuroscience and Pharmacology, Faculty of Medic
  • Schwartz TW; Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Receptology and Enteroendocrinology, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Denmark; Laboratory for Molecular Pharmacology, Department of Neuroscience and Pharmacology, Faculty of Medic
  • Cox HM; King's College London, Wolfson Centre for Age-Related Diseases, Guy's Campus, London SE1 1UL, UK.
  • Cone RD; Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA. Electronic address: roger.cone@vanderbilt.edu.
Cell Metab ; 20(6): 1018-29, 2014 Dec 02.
Article em En | MEDLINE | ID: mdl-25453189
ABSTRACT
The melanocortin-4 receptor (MC4R) is expressed in the brainstem and vagal afferent nerves and regulates a number of aspects of gastrointestinal function. Here we show that the receptor is also diffusely expressed in cells of the gastrointestinal system, from stomach to descending colon. Furthermore, MC4R is the second most highly enriched GPCR in peptide YY (PYY) and glucagon-like peptide 1 (GLP-1) expressing enteroendocrine L cells. When vectorial ion transport is measured across mouse or human intestinal mucosa, administration of α-MSH induces a MC4R-specific PYY-dependent antisecretory response consistent with a role for the MC4R in paracrine inhibition of electrolyte secretion. Finally, MC4R-dependent acute PYY and GLP-1 release from L cells can be stimulated in vivo by intraperitoneal (i.p.) administration of melanocortin peptides to mice. This suggests physiological significance for MC4R in L cells and indicates a previously unrecognized peripheral role for the MC4R, complementing vagal and central receptor functions.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Enteroendócrinas / Peptídeo YY / Receptor Tipo 4 de Melanocortina / Peptídeo 1 Semelhante ao Glucagon Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Enteroendócrinas / Peptídeo YY / Receptor Tipo 4 de Melanocortina / Peptídeo 1 Semelhante ao Glucagon Idioma: En Ano de publicação: 2014 Tipo de documento: Article