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RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes
Glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are gastrointestinal hormones that play an important role in stimulating postprandial insulin release from pancreatic β-cells. Agents that either mimic GLP-1 or prevent its degradation are now available for the tr...
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613238/ https://www.ncbi.nlm.nih.gov/pubmed/18959599 http://dx.doi.org/10.1111/j.1464-5491.2008.02514.x |
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author | Gribble, F M |
author_facet | Gribble, F M |
author_sort | Gribble, F M |
collection | PubMed |
description | Glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are gastrointestinal hormones that play an important role in stimulating postprandial insulin release from pancreatic β-cells. Agents that either mimic GLP-1 or prevent its degradation are now available for the treatment of Type 2 diabetes, and strategies to enhance endogenous GLP-1 release are under assessment. As intestinal peptides have a range of actions, including appetite regulation and coordination of fat metabolism, harnessing the enteric endocrine system is a promising new field for drug development. Diabet. Med. 25, 889–894 (2008) |
format | Text |
id | pubmed-2613238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-26132382009-01-12 RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes Gribble, F M Diabet Med Review Article Glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are gastrointestinal hormones that play an important role in stimulating postprandial insulin release from pancreatic β-cells. Agents that either mimic GLP-1 or prevent its degradation are now available for the treatment of Type 2 diabetes, and strategies to enhance endogenous GLP-1 release are under assessment. As intestinal peptides have a range of actions, including appetite regulation and coordination of fat metabolism, harnessing the enteric endocrine system is a promising new field for drug development. Diabet. Med. 25, 889–894 (2008) Blackwell Publishing Ltd 2008-08 /pmc/articles/PMC2613238/ /pubmed/18959599 http://dx.doi.org/10.1111/j.1464-5491.2008.02514.x Text en © 2008 The Author. Journal compilation © 2008 Diabetes UK. |
spellingShingle | Review Article Gribble, F M RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes |
title | RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes |
title_full | RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes |
title_fullStr | RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes |
title_full_unstemmed | RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes |
title_short | RD Lawrence Lecture 2008 Targeting GLP-1 release as a potential strategy for the therapy of Type 2 diabetes |
title_sort | rd lawrence lecture 2008 targeting glp-1 release as a potential strategy for the therapy of type 2 diabetes |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613238/ https://www.ncbi.nlm.nih.gov/pubmed/18959599 http://dx.doi.org/10.1111/j.1464-5491.2008.02514.x |
work_keys_str_mv | AT gribblefm rdlawrencelecture2008targetingglp1releaseasapotentialstrategyforthetherapyoftype2diabetes |