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Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin
Metformin, the most widely prescribed drug therapy for type 2 diabetes, has pleiotropic benefits, in addition to its capacity to lower elevated blood glucose levels, including mitigation of cardiovascular risk. The mechanisms underlying the latter remain unclear. Mechanistic studies have, hitherto,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700183/ https://www.ncbi.nlm.nih.gov/pubmed/33266396 http://dx.doi.org/10.3390/ph13110410 |
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author | Borg, Malcolm J. Rayner, Christopher K. Jones, Karen L. Horowitz, Michael Xie, Cong Wu, Tongzhi |
author_facet | Borg, Malcolm J. Rayner, Christopher K. Jones, Karen L. Horowitz, Michael Xie, Cong Wu, Tongzhi |
author_sort | Borg, Malcolm J. |
collection | PubMed |
description | Metformin, the most widely prescribed drug therapy for type 2 diabetes, has pleiotropic benefits, in addition to its capacity to lower elevated blood glucose levels, including mitigation of cardiovascular risk. The mechanisms underlying the latter remain unclear. Mechanistic studies have, hitherto, focused on the direct effects of metformin on the heart and vasculature. It is now appreciated that effects in the gastrointestinal tract are important to glucose-lowering by metformin. Gastrointestinal actions of metformin also have major implications for cardiovascular function. This review summarizes the gastrointestinal mechanisms underlying the action of metformin and their potential relevance to cardiovascular benefits. |
format | Online Article Text |
id | pubmed-7700183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77001832020-11-30 Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin Borg, Malcolm J. Rayner, Christopher K. Jones, Karen L. Horowitz, Michael Xie, Cong Wu, Tongzhi Pharmaceuticals (Basel) Review Metformin, the most widely prescribed drug therapy for type 2 diabetes, has pleiotropic benefits, in addition to its capacity to lower elevated blood glucose levels, including mitigation of cardiovascular risk. The mechanisms underlying the latter remain unclear. Mechanistic studies have, hitherto, focused on the direct effects of metformin on the heart and vasculature. It is now appreciated that effects in the gastrointestinal tract are important to glucose-lowering by metformin. Gastrointestinal actions of metformin also have major implications for cardiovascular function. This review summarizes the gastrointestinal mechanisms underlying the action of metformin and their potential relevance to cardiovascular benefits. MDPI 2020-11-22 /pmc/articles/PMC7700183/ /pubmed/33266396 http://dx.doi.org/10.3390/ph13110410 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Borg, Malcolm J. Rayner, Christopher K. Jones, Karen L. Horowitz, Michael Xie, Cong Wu, Tongzhi Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin |
title | Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin |
title_full | Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin |
title_fullStr | Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin |
title_full_unstemmed | Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin |
title_short | Gastrointestinal Mechanisms Underlying the Cardiovascular Effect of Metformin |
title_sort | gastrointestinal mechanisms underlying the cardiovascular effect of metformin |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700183/ https://www.ncbi.nlm.nih.gov/pubmed/33266396 http://dx.doi.org/10.3390/ph13110410 |
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