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Advanced glycation end products, oxidative stress and diabetic nephropathy

About 246 million people worldwide had diabetes in 2007. The global figure of people with diabetes is projected to increase to 370 million in 2030. As the prevalence of diabetes has risen to epidemic proportions worldwide, diabetic nephropathy has become one of the most challenging health problems....

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Detalles Bibliográficos
Autores principales: Yamagishi, Sho-ichi, Matsui, Takanori
Formato: Texto
Lenguaje:English
Publicado: Landes Bioscience 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952094/
https://www.ncbi.nlm.nih.gov/pubmed/20716934
http://dx.doi.org/10.4161/oxim.3.2.4
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author Yamagishi, Sho-ichi
Matsui, Takanori
author_facet Yamagishi, Sho-ichi
Matsui, Takanori
author_sort Yamagishi, Sho-ichi
collection PubMed
description About 246 million people worldwide had diabetes in 2007. The global figure of people with diabetes is projected to increase to 370 million in 2030. As the prevalence of diabetes has risen to epidemic proportions worldwide, diabetic nephropathy has become one of the most challenging health problems. Therapeutic options such as strict blood glucose and blood pressure controls are effective for preventing diabetic nephropathy, but are far from satisfactory, and the number of diabetic patients on end-stage renal disease is still increasing. Therefore, a novel therapeutic strategy that could halt the progression of diabetic nephropathy should be developed. There is accumulating evidence that advanced glycation end products (AGEs), senescent macroprotein derivatives formed at an accelerated rate under diabetes, play a role in diabetic nephropathy via oxidative stress generation. In this paper, we review the pathophysiological role of AGEs and their receptor (RAGE)-oxidative stress system in diabetic nephropathy.
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spelling pubmed-29520942011-03-01 Advanced glycation end products, oxidative stress and diabetic nephropathy Yamagishi, Sho-ichi Matsui, Takanori Oxid Med Cell Longev Reviews About 246 million people worldwide had diabetes in 2007. The global figure of people with diabetes is projected to increase to 370 million in 2030. As the prevalence of diabetes has risen to epidemic proportions worldwide, diabetic nephropathy has become one of the most challenging health problems. Therapeutic options such as strict blood glucose and blood pressure controls are effective for preventing diabetic nephropathy, but are far from satisfactory, and the number of diabetic patients on end-stage renal disease is still increasing. Therefore, a novel therapeutic strategy that could halt the progression of diabetic nephropathy should be developed. There is accumulating evidence that advanced glycation end products (AGEs), senescent macroprotein derivatives formed at an accelerated rate under diabetes, play a role in diabetic nephropathy via oxidative stress generation. In this paper, we review the pathophysiological role of AGEs and their receptor (RAGE)-oxidative stress system in diabetic nephropathy. Landes Bioscience 2010 /pmc/articles/PMC2952094/ /pubmed/20716934 http://dx.doi.org/10.4161/oxim.3.2.4 Text en Copyright © 2010 Landes Bioscience
spellingShingle Reviews
Yamagishi, Sho-ichi
Matsui, Takanori
Advanced glycation end products, oxidative stress and diabetic nephropathy
title Advanced glycation end products, oxidative stress and diabetic nephropathy
title_full Advanced glycation end products, oxidative stress and diabetic nephropathy
title_fullStr Advanced glycation end products, oxidative stress and diabetic nephropathy
title_full_unstemmed Advanced glycation end products, oxidative stress and diabetic nephropathy
title_short Advanced glycation end products, oxidative stress and diabetic nephropathy
title_sort advanced glycation end products, oxidative stress and diabetic nephropathy
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952094/
https://www.ncbi.nlm.nih.gov/pubmed/20716934
http://dx.doi.org/10.4161/oxim.3.2.4
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