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Recent Advances in Potential Clinical Application of Ghrelin in Obesity

Ghrelin is the natural ligand of the growth hormone secretagogue receptor (GHS-R1a). Ghrelin is a 28 amino acid peptide possessing a unique acylation on the serine in position 3 catalyzed by ghrelin O-acyltransferase (GOAT). Ghrelin stimulates growth hormone secretion, but also appetite, food intake...

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Detalles Bibliográficos
Autor principal: Delporte, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317165/
https://www.ncbi.nlm.nih.gov/pubmed/22523666
http://dx.doi.org/10.1155/2012/535624
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author Delporte, Christine
author_facet Delporte, Christine
author_sort Delporte, Christine
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description Ghrelin is the natural ligand of the growth hormone secretagogue receptor (GHS-R1a). Ghrelin is a 28 amino acid peptide possessing a unique acylation on the serine in position 3 catalyzed by ghrelin O-acyltransferase (GOAT). Ghrelin stimulates growth hormone secretion, but also appetite, food intake, weight gain, and gastric emptying. Ghrelin is involved in weight regulation, obesity, type 2 diabetes, and metabolic syndrome. Furthermore, a better understanding of ghrelin biology led to the identification of molecular targets modulating ghrelin levels and/or its biological effects: GOAT, ghrelin, and GHS-R1a. Furthermore, a recent discovery, showing the involvement of bitter taste receptor T2R in ghrelin secretion and/or synthesis and food intake, suggested that T2R could represent an additional interesting molecular target. Several classes of ghrelin-related pharmacological tools for the treatment of obesity have been or could be developed to modulate the identified molecular targets.
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spelling pubmed-33171652012-04-20 Recent Advances in Potential Clinical Application of Ghrelin in Obesity Delporte, Christine J Obes Review Article Ghrelin is the natural ligand of the growth hormone secretagogue receptor (GHS-R1a). Ghrelin is a 28 amino acid peptide possessing a unique acylation on the serine in position 3 catalyzed by ghrelin O-acyltransferase (GOAT). Ghrelin stimulates growth hormone secretion, but also appetite, food intake, weight gain, and gastric emptying. Ghrelin is involved in weight regulation, obesity, type 2 diabetes, and metabolic syndrome. Furthermore, a better understanding of ghrelin biology led to the identification of molecular targets modulating ghrelin levels and/or its biological effects: GOAT, ghrelin, and GHS-R1a. Furthermore, a recent discovery, showing the involvement of bitter taste receptor T2R in ghrelin secretion and/or synthesis and food intake, suggested that T2R could represent an additional interesting molecular target. Several classes of ghrelin-related pharmacological tools for the treatment of obesity have been or could be developed to modulate the identified molecular targets. Hindawi Publishing Corporation 2012 2012-02-20 /pmc/articles/PMC3317165/ /pubmed/22523666 http://dx.doi.org/10.1155/2012/535624 Text en Copyright © 2012 Christine Delporte. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Delporte, Christine
Recent Advances in Potential Clinical Application of Ghrelin in Obesity
title Recent Advances in Potential Clinical Application of Ghrelin in Obesity
title_full Recent Advances in Potential Clinical Application of Ghrelin in Obesity
title_fullStr Recent Advances in Potential Clinical Application of Ghrelin in Obesity
title_full_unstemmed Recent Advances in Potential Clinical Application of Ghrelin in Obesity
title_short Recent Advances in Potential Clinical Application of Ghrelin in Obesity
title_sort recent advances in potential clinical application of ghrelin in obesity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317165/
https://www.ncbi.nlm.nih.gov/pubmed/22523666
http://dx.doi.org/10.1155/2012/535624
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