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Glucagon-Like Peptide-1 Gene Therapy

Glucagon-like peptide 1 (GLP-1) is a small peptide component of the prohormone, proglucagon, that is produced in the gut. Exendin-4, a GLP-1 receptor agonist originally isolated from the saliva of H. suspectum or Gila monster, is a peptide that shares sequence and functional homology with GLP-1. Bot...

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Autores principales: Rowzee, Anne M., Cawley, Niamh X., Chiorini, John A., Di Pasquale, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124282/
https://www.ncbi.nlm.nih.gov/pubmed/21747830
http://dx.doi.org/10.1155/2011/601047
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author Rowzee, Anne M.
Cawley, Niamh X.
Chiorini, John A.
Di Pasquale, Giovanni
author_facet Rowzee, Anne M.
Cawley, Niamh X.
Chiorini, John A.
Di Pasquale, Giovanni
author_sort Rowzee, Anne M.
collection PubMed
description Glucagon-like peptide 1 (GLP-1) is a small peptide component of the prohormone, proglucagon, that is produced in the gut. Exendin-4, a GLP-1 receptor agonist originally isolated from the saliva of H. suspectum or Gila monster, is a peptide that shares sequence and functional homology with GLP-1. Both peptides have been demonstrated to stimulate insulin secretion, inhibit glucagon secretion, promote satiety and slow gastric emptying. As such, GLP-1 and Exendin-4 have become attractive pharmaceutical targets as an adjunctive therapy for individuals with type II diabetes mellitus, with several products currently available clinically. Herein we summarize the cell biology leading to GLP-1 production and secretion from intestinal L-cells and the endocrine functions of this peptide and Exendin-4 in humans. Additionally, gene therapeutic applications of GLP-1 and Exendin-4 are discussed with a focus on recent work using the salivary gland as a gene therapy target organ for the treatment of diabetes mellitus.
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spelling pubmed-31242822011-07-11 Glucagon-Like Peptide-1 Gene Therapy Rowzee, Anne M. Cawley, Niamh X. Chiorini, John A. Di Pasquale, Giovanni Exp Diabetes Res Review Article Glucagon-like peptide 1 (GLP-1) is a small peptide component of the prohormone, proglucagon, that is produced in the gut. Exendin-4, a GLP-1 receptor agonist originally isolated from the saliva of H. suspectum or Gila monster, is a peptide that shares sequence and functional homology with GLP-1. Both peptides have been demonstrated to stimulate insulin secretion, inhibit glucagon secretion, promote satiety and slow gastric emptying. As such, GLP-1 and Exendin-4 have become attractive pharmaceutical targets as an adjunctive therapy for individuals with type II diabetes mellitus, with several products currently available clinically. Herein we summarize the cell biology leading to GLP-1 production and secretion from intestinal L-cells and the endocrine functions of this peptide and Exendin-4 in humans. Additionally, gene therapeutic applications of GLP-1 and Exendin-4 are discussed with a focus on recent work using the salivary gland as a gene therapy target organ for the treatment of diabetes mellitus. Hindawi Publishing Corporation 2011 2011-06-20 /pmc/articles/PMC3124282/ /pubmed/21747830 http://dx.doi.org/10.1155/2011/601047 Text en Copyright © 2011 Anne M. Rowzee et al. https://creativecommons.org/licenses/by/3.0/ 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
Rowzee, Anne M.
Cawley, Niamh X.
Chiorini, John A.
Di Pasquale, Giovanni
Glucagon-Like Peptide-1 Gene Therapy
title Glucagon-Like Peptide-1 Gene Therapy
title_full Glucagon-Like Peptide-1 Gene Therapy
title_fullStr Glucagon-Like Peptide-1 Gene Therapy
title_full_unstemmed Glucagon-Like Peptide-1 Gene Therapy
title_short Glucagon-Like Peptide-1 Gene Therapy
title_sort glucagon-like peptide-1 gene therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124282/
https://www.ncbi.nlm.nih.gov/pubmed/21747830
http://dx.doi.org/10.1155/2011/601047
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