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Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control

Dipeptidyl peptidase (DPP)-4 inhibitors are oral anti-diabetic medications that block the activity of the ubiquitous enzyme DPP-4. Inhibition of this enzyme increases the level of circulating active glucagon-like peptide (GLP)-1 secreted from L-cells in the small intestine. GLP-1 increases the gluco...

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Autores principales: Kang, Seon Mee, Park, Jeong Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558587/
https://www.ncbi.nlm.nih.gov/pubmed/34733107
http://dx.doi.org/10.1177/11795514211051698
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author Kang, Seon Mee
Park, Jeong Hyun
author_facet Kang, Seon Mee
Park, Jeong Hyun
author_sort Kang, Seon Mee
collection PubMed
description Dipeptidyl peptidase (DPP)-4 inhibitors are oral anti-diabetic medications that block the activity of the ubiquitous enzyme DPP-4. Inhibition of this enzyme increases the level of circulating active glucagon-like peptide (GLP)-1 secreted from L-cells in the small intestine. GLP-1 increases the glucose level, dependent on insulin secretion from pancreatic β-cells; it also decreases the abnormally increased level of glucagon, eventually decreasing the blood glucose level in patients with type 2 diabetes. DPP-4 is involved in many physiological processes other than the degradation of GLP-1. Therefore, the inhibition of DPP-4 may have numerous effects beyond glucose control. In this article, we review the pleiotropic effects of DPP-4 inhibitors beyond glucose control, including their strong beneficial effects on the stress induced accelerated senescence of vascular cells, and the possible clinical implications of these effects.
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spelling pubmed-85585872021-11-02 Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control Kang, Seon Mee Park, Jeong Hyun Clin Med Insights Endocrinol Diabetes Review Article Dipeptidyl peptidase (DPP)-4 inhibitors are oral anti-diabetic medications that block the activity of the ubiquitous enzyme DPP-4. Inhibition of this enzyme increases the level of circulating active glucagon-like peptide (GLP)-1 secreted from L-cells in the small intestine. GLP-1 increases the glucose level, dependent on insulin secretion from pancreatic β-cells; it also decreases the abnormally increased level of glucagon, eventually decreasing the blood glucose level in patients with type 2 diabetes. DPP-4 is involved in many physiological processes other than the degradation of GLP-1. Therefore, the inhibition of DPP-4 may have numerous effects beyond glucose control. In this article, we review the pleiotropic effects of DPP-4 inhibitors beyond glucose control, including their strong beneficial effects on the stress induced accelerated senescence of vascular cells, and the possible clinical implications of these effects. SAGE Publications 2021-10-28 /pmc/articles/PMC8558587/ /pubmed/34733107 http://dx.doi.org/10.1177/11795514211051698 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review Article
Kang, Seon Mee
Park, Jeong Hyun
Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control
title Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control
title_full Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control
title_fullStr Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control
title_full_unstemmed Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control
title_short Pleiotropic Benefits of DPP-4 Inhibitors Beyond Glycemic Control
title_sort pleiotropic benefits of dpp-4 inhibitors beyond glycemic control
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558587/
https://www.ncbi.nlm.nih.gov/pubmed/34733107
http://dx.doi.org/10.1177/11795514211051698
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