New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy

Diabetic nephropathy (DN) is a severe complication of diabetes and serves as the leading cause of chronic renal failure. In the past decades, angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin II receptor blockers (ARBs) based first-line therapy can slow but cannot stop the progression of...

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Main Authors: Zhanjun Jia, Ying Sun, Guangrui Yang, Aihua Zhang, Songming Huang, Kristina Marie Heiney, Yue Zhang
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:PPAR Research
Online Access:http://dx.doi.org/10.1155/2014/818530
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author Zhanjun Jia
Ying Sun
Guangrui Yang
Aihua Zhang
Songming Huang
Kristina Marie Heiney
Yue Zhang
author_facet Zhanjun Jia
Ying Sun
Guangrui Yang
Aihua Zhang
Songming Huang
Kristina Marie Heiney
Yue Zhang
author_sort Zhanjun Jia
collection DOAJ
description Diabetic nephropathy (DN) is a severe complication of diabetes and serves as the leading cause of chronic renal failure. In the past decades, angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin II receptor blockers (ARBs) based first-line therapy can slow but cannot stop the progression of DN, which urgently requests the innovation of therapeutic strategies. Thiazolidinediones (TZDs), the synthetic exogenous ligands of nuclear receptor peroxisome proliferator-activated receptor-γ (PPARγ), had been thought to be a promising candidate for strengthening the therapy of DN. However, the severe adverse effects including fluid retention, cardiovascular complications, and bone loss greatly limited their use in clinic. Recently, numerous novel PPARγ agonists involving the endogenous PPARγ ligands and selective PPARγ modulators (SPPARMs) are emerging as the promising candidates of the next generation of antidiabetic drugs instead of TZDs. Due to the higher selectivity of these novel PPARγ agonists on the regulation of the antidiabetes-associated genes than that of the side effect-associated genes, they present fewer adverse effects than TZDs. The present review was undertaken to address the advancements and the therapeutic potential of these newly developed PPARγ agonists in dealing with diabetic kidney disease. At the same time, the new insights into the therapeutic strategies of DN based on the PPARγ agonists were fully addressed.
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series PPAR Research
spelling doaj-art-a9d3520d1aad4aeb949e952bc12b51fe2025-02-03T01:00:49ZengWileyPPAR Research1687-47571687-47652014-01-01201410.1155/2014/818530818530New Insights into the PPARγ Agonists for the Treatment of Diabetic NephropathyZhanjun Jia0Ying Sun1Guangrui Yang2Aihua Zhang3Songming Huang4Kristina Marie Heiney5Yue Zhang6Department of Nephrology, Nanjing Children’s Hospital, Nanjing Medical University, Nanjing 210008, ChinaDepartment of Nephrology, Nanjing Children’s Hospital, Nanjing Medical University, Nanjing 210008, ChinaInstitute for Translational Medicine and Therapeutics, University of Pennsylvania, Philadelphia, PA 19104, USADepartment of Nephrology, Nanjing Children’s Hospital, Nanjing Medical University, Nanjing 210008, ChinaDepartment of Nephrology, Nanjing Children’s Hospital, Nanjing Medical University, Nanjing 210008, ChinaDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84132, USADepartment of Nephrology, Nanjing Children’s Hospital, Nanjing Medical University, Nanjing 210008, ChinaDiabetic nephropathy (DN) is a severe complication of diabetes and serves as the leading cause of chronic renal failure. In the past decades, angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin II receptor blockers (ARBs) based first-line therapy can slow but cannot stop the progression of DN, which urgently requests the innovation of therapeutic strategies. Thiazolidinediones (TZDs), the synthetic exogenous ligands of nuclear receptor peroxisome proliferator-activated receptor-γ (PPARγ), had been thought to be a promising candidate for strengthening the therapy of DN. However, the severe adverse effects including fluid retention, cardiovascular complications, and bone loss greatly limited their use in clinic. Recently, numerous novel PPARγ agonists involving the endogenous PPARγ ligands and selective PPARγ modulators (SPPARMs) are emerging as the promising candidates of the next generation of antidiabetic drugs instead of TZDs. Due to the higher selectivity of these novel PPARγ agonists on the regulation of the antidiabetes-associated genes than that of the side effect-associated genes, they present fewer adverse effects than TZDs. The present review was undertaken to address the advancements and the therapeutic potential of these newly developed PPARγ agonists in dealing with diabetic kidney disease. At the same time, the new insights into the therapeutic strategies of DN based on the PPARγ agonists were fully addressed.http://dx.doi.org/10.1155/2014/818530
spellingShingle Zhanjun Jia
Ying Sun
Guangrui Yang
Aihua Zhang
Songming Huang
Kristina Marie Heiney
Yue Zhang
New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy
PPAR Research
title New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy
title_full New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy
title_fullStr New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy
title_full_unstemmed New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy
title_short New Insights into the PPARγ Agonists for the Treatment of Diabetic Nephropathy
title_sort new insights into the pparγ agonists for the treatment of diabetic nephropathy
url http://dx.doi.org/10.1155/2014/818530
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