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Renoprotective Effects of DPP-4 Inhibitors
Diabetic kidney disease (DKD) is the leading cause of end-stage renal disease (ESRD) worldwide. Dipeptidyl peptidase (DPP)-4 inhibitors are widely used in the treatment of patients with type 2 diabetes (T2D). DPP-4 inhibitors reduce glucose levels by inhibiting degradation of incretins. DPP-4 is a u...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915260/ https://www.ncbi.nlm.nih.gov/pubmed/33562528 http://dx.doi.org/10.3390/antiox10020246 |
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author | Kawanami, Daiji Takashi, Yuichi Takahashi, Hiroyuki Motonaga, Ryoko Tanabe, Makito |
author_facet | Kawanami, Daiji Takashi, Yuichi Takahashi, Hiroyuki Motonaga, Ryoko Tanabe, Makito |
author_sort | Kawanami, Daiji |
collection | PubMed |
description | Diabetic kidney disease (DKD) is the leading cause of end-stage renal disease (ESRD) worldwide. Dipeptidyl peptidase (DPP)-4 inhibitors are widely used in the treatment of patients with type 2 diabetes (T2D). DPP-4 inhibitors reduce glucose levels by inhibiting degradation of incretins. DPP-4 is a ubiquitous protein with exopeptidase activity that exists in cell membrane-bound and soluble forms. It has been shown that an increased renal DPP-4 activity is associated with the development of DKD. A series of clinical and experimental studies showed that DPP-4 inhibitors have beneficial effects on DKD, independent of their glucose-lowering abilities, which are mediated by anti-fibrotic, anti-inflammatory, and anti-oxidative stress properties. In this review article, we highlight the current understanding of the clinical efficacy and the mechanisms underlying renoprotection by DPP-4 inhibitors under diabetic conditions. |
format | Online Article Text |
id | pubmed-7915260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79152602021-03-01 Renoprotective Effects of DPP-4 Inhibitors Kawanami, Daiji Takashi, Yuichi Takahashi, Hiroyuki Motonaga, Ryoko Tanabe, Makito Antioxidants (Basel) Review Diabetic kidney disease (DKD) is the leading cause of end-stage renal disease (ESRD) worldwide. Dipeptidyl peptidase (DPP)-4 inhibitors are widely used in the treatment of patients with type 2 diabetes (T2D). DPP-4 inhibitors reduce glucose levels by inhibiting degradation of incretins. DPP-4 is a ubiquitous protein with exopeptidase activity that exists in cell membrane-bound and soluble forms. It has been shown that an increased renal DPP-4 activity is associated with the development of DKD. A series of clinical and experimental studies showed that DPP-4 inhibitors have beneficial effects on DKD, independent of their glucose-lowering abilities, which are mediated by anti-fibrotic, anti-inflammatory, and anti-oxidative stress properties. In this review article, we highlight the current understanding of the clinical efficacy and the mechanisms underlying renoprotection by DPP-4 inhibitors under diabetic conditions. MDPI 2021-02-05 /pmc/articles/PMC7915260/ /pubmed/33562528 http://dx.doi.org/10.3390/antiox10020246 Text en © 2021 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 Kawanami, Daiji Takashi, Yuichi Takahashi, Hiroyuki Motonaga, Ryoko Tanabe, Makito Renoprotective Effects of DPP-4 Inhibitors |
title | Renoprotective Effects of DPP-4 Inhibitors |
title_full | Renoprotective Effects of DPP-4 Inhibitors |
title_fullStr | Renoprotective Effects of DPP-4 Inhibitors |
title_full_unstemmed | Renoprotective Effects of DPP-4 Inhibitors |
title_short | Renoprotective Effects of DPP-4 Inhibitors |
title_sort | renoprotective effects of dpp-4 inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915260/ https://www.ncbi.nlm.nih.gov/pubmed/33562528 http://dx.doi.org/10.3390/antiox10020246 |
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