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Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies
A new strategy under development for the treatment of type 2 diabetes and obesity is to mimic some of the effects of bariatric surgery by delivering food-related stimuli to the distal gastrointestinal tract where they should enhance the release of gut hormones such as glucagon-like peptide-1 (GLP-1)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805852/ https://www.ncbi.nlm.nih.gov/pubmed/29412834 http://dx.doi.org/10.1016/j.peptides.2017.11.008 |
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author | Gribble, Fiona M. Meek, Claire L. Reimann, Frank |
author_facet | Gribble, Fiona M. Meek, Claire L. Reimann, Frank |
author_sort | Gribble, Fiona M. |
collection | PubMed |
description | A new strategy under development for the treatment of type 2 diabetes and obesity is to mimic some of the effects of bariatric surgery by delivering food-related stimuli to the distal gastrointestinal tract where they should enhance the release of gut hormones such as glucagon-like peptide-1 (GLP-1) and peptideYY (PYY). Methods include inhibition of food digestion and absorption in the upper GI tract, or oral delivery of stimuli in capsules or pelleted form to protect them against gastric degradation. A variety of agents have been tested in humans using capsules, microcapsules or pellets, delivering nutrients, bile acids, fatty acids and bitter compounds. This review examines the outcomes of these different approaches and supporting evidence from intestinal perfusion studies. |
format | Online Article Text |
id | pubmed-5805852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Science Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-58058522018-02-13 Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies Gribble, Fiona M. Meek, Claire L. Reimann, Frank Peptides Article A new strategy under development for the treatment of type 2 diabetes and obesity is to mimic some of the effects of bariatric surgery by delivering food-related stimuli to the distal gastrointestinal tract where they should enhance the release of gut hormones such as glucagon-like peptide-1 (GLP-1) and peptideYY (PYY). Methods include inhibition of food digestion and absorption in the upper GI tract, or oral delivery of stimuli in capsules or pelleted form to protect them against gastric degradation. A variety of agents have been tested in humans using capsules, microcapsules or pellets, delivering nutrients, bile acids, fatty acids and bitter compounds. This review examines the outcomes of these different approaches and supporting evidence from intestinal perfusion studies. Elsevier Science Inc 2018-02 /pmc/articles/PMC5805852/ /pubmed/29412834 http://dx.doi.org/10.1016/j.peptides.2017.11.008 Text en © 2017 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gribble, Fiona M. Meek, Claire L. Reimann, Frank Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
title | Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
title_full | Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
title_fullStr | Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
title_full_unstemmed | Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
title_short | Targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
title_sort | targeted intestinal delivery of incretin secretagogues—towards new diabetes and obesity therapies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805852/ https://www.ncbi.nlm.nih.gov/pubmed/29412834 http://dx.doi.org/10.1016/j.peptides.2017.11.008 |
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