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Liraglutide in the management of type 2 diabetes
The pathophysiology of type 2 diabetes has been attributed to the classic triad of decreased insulin secretion, increased insulin resistance, and elevated hepatic glucose production. Research has shown additional mechanisms, including incretin deficiency or resistance in the gastrointestinal tract....
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990388/ https://www.ncbi.nlm.nih.gov/pubmed/21116334 http://dx.doi.org/10.2147/DDDT.S10180 |
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author | Wajcberg, Estela Amarah, Amatur |
author_facet | Wajcberg, Estela Amarah, Amatur |
author_sort | Wajcberg, Estela |
collection | PubMed |
description | The pathophysiology of type 2 diabetes has been attributed to the classic triad of decreased insulin secretion, increased insulin resistance, and elevated hepatic glucose production. Research has shown additional mechanisms, including incretin deficiency or resistance in the gastrointestinal tract. Liraglutide is a modified form of human glucagon-like peptide-1. Liraglutide was obtained by substitution of lysine 34 for arginine near the NH2 terminus, and by addition of a C16 fatty acid at the ɛ-amino group of lysine (at position 26) using a γ-glutamic acid spacer. Liraglutide has demonstrated glucose-dependent insulin secretion, improvements in β-cell function, deceleration of gastric emptying, and promotion of early satiety leading to weight loss. Liraglutide has the potential to acquire an important role, not only in the treatment of type 2 diabetes, but also in preservation of β-cell function, weight loss, and prevention of chronic diabetic complications. |
format | Text |
id | pubmed-2990388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29903882010-11-29 Liraglutide in the management of type 2 diabetes Wajcberg, Estela Amarah, Amatur Drug Des Devel Ther Review The pathophysiology of type 2 diabetes has been attributed to the classic triad of decreased insulin secretion, increased insulin resistance, and elevated hepatic glucose production. Research has shown additional mechanisms, including incretin deficiency or resistance in the gastrointestinal tract. Liraglutide is a modified form of human glucagon-like peptide-1. Liraglutide was obtained by substitution of lysine 34 for arginine near the NH2 terminus, and by addition of a C16 fatty acid at the ɛ-amino group of lysine (at position 26) using a γ-glutamic acid spacer. Liraglutide has demonstrated glucose-dependent insulin secretion, improvements in β-cell function, deceleration of gastric emptying, and promotion of early satiety leading to weight loss. Liraglutide has the potential to acquire an important role, not only in the treatment of type 2 diabetes, but also in preservation of β-cell function, weight loss, and prevention of chronic diabetic complications. Dove Medical Press 2010-10-22 /pmc/articles/PMC2990388/ /pubmed/21116334 http://dx.doi.org/10.2147/DDDT.S10180 Text en © 2010 Wajcberg and Amarah, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Review Wajcberg, Estela Amarah, Amatur Liraglutide in the management of type 2 diabetes |
title | Liraglutide in the management of type 2 diabetes |
title_full | Liraglutide in the management of type 2 diabetes |
title_fullStr | Liraglutide in the management of type 2 diabetes |
title_full_unstemmed | Liraglutide in the management of type 2 diabetes |
title_short | Liraglutide in the management of type 2 diabetes |
title_sort | liraglutide in the management of type 2 diabetes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990388/ https://www.ncbi.nlm.nih.gov/pubmed/21116334 http://dx.doi.org/10.2147/DDDT.S10180 |
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