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The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill

Glucagon-like peptide-1 (GLP-1), a principal mediator of the postprandial insulinotropic response in health, has a half-life of minutes. The saliva of the Gila monster contains exendin-4, a structural analogue of human GLP-1, but with a much longer half-life. A synthetic preparation of exendin-4, ex...

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Detalles Bibliográficos
Autores principales: Deane, Adam M, Chapman, Marianne J, Horowitz, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219279/
https://www.ncbi.nlm.nih.gov/pubmed/20979668
http://dx.doi.org/10.1186/cc9281
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author Deane, Adam M
Chapman, Marianne J
Horowitz, Michael
author_facet Deane, Adam M
Chapman, Marianne J
Horowitz, Michael
author_sort Deane, Adam M
collection PubMed
description Glucagon-like peptide-1 (GLP-1), a principal mediator of the postprandial insulinotropic response in health, has a half-life of minutes. The saliva of the Gila monster contains exendin-4, a structural analogue of human GLP-1, but with a much longer half-life. A synthetic preparation of exendin-4, exenatide, is suitable for human use and effectively lowers glucose in ambulant type 2 diabetic patients. When compared with insulin, exenatide therapy is associated with a reduction in hypoglycaemic episodes and postprandial glycaemic excursions in this group. Accordingly, GLP-1 analogues are appealing therapies for hyperglycaemia in the critically ill patient and warrant further study.
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spelling pubmed-32192792011-11-18 The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill Deane, Adam M Chapman, Marianne J Horowitz, Michael Crit Care Commentary Glucagon-like peptide-1 (GLP-1), a principal mediator of the postprandial insulinotropic response in health, has a half-life of minutes. The saliva of the Gila monster contains exendin-4, a structural analogue of human GLP-1, but with a much longer half-life. A synthetic preparation of exendin-4, exenatide, is suitable for human use and effectively lowers glucose in ambulant type 2 diabetic patients. When compared with insulin, exenatide therapy is associated with a reduction in hypoglycaemic episodes and postprandial glycaemic excursions in this group. Accordingly, GLP-1 analogues are appealing therapies for hyperglycaemia in the critically ill patient and warrant further study. BioMed Central 2010 2010-10-21 /pmc/articles/PMC3219279/ /pubmed/20979668 http://dx.doi.org/10.1186/cc9281 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Commentary
Deane, Adam M
Chapman, Marianne J
Horowitz, Michael
The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
title The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
title_full The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
title_fullStr The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
title_full_unstemmed The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
title_short The therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
title_sort therapeutic potential of a venomous lizard: the use of glucagon-like peptide-1 analogues in the critically ill
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219279/
https://www.ncbi.nlm.nih.gov/pubmed/20979668
http://dx.doi.org/10.1186/cc9281
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