Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism

PPARγ (peroxisome proliferator activated receptor γ) is a ligand activated transcription factor of the nuclear receptor superfamily that controls the expression of a variety of genes involved in fatty acid metabolism, adipogenesis, and insulin sensitivity. While endogenous ligands of PPARγ include f...

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Main Authors: Alice J. Kroker, John B. Bruning
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:PPAR Research
Online Access:http://dx.doi.org/10.1155/2015/816856
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author Alice J. Kroker
John B. Bruning
author_facet Alice J. Kroker
John B. Bruning
author_sort Alice J. Kroker
collection DOAJ
description PPARγ (peroxisome proliferator activated receptor γ) is a ligand activated transcription factor of the nuclear receptor superfamily that controls the expression of a variety of genes involved in fatty acid metabolism, adipogenesis, and insulin sensitivity. While endogenous ligands of PPARγ include fatty acids and eicosanoids, synthetic full agonists of the receptor, including members of the thiazolidinedione (TZD) class, have been widely prescribed for the treatment of type II diabetes mellitus (T2DM). Unfortunately, the use of full agonists has been hampered by harsh side effects with some removed from the market in many countries. In contrast, partial agonists of PPARγ have been shown to retain favourable insulin sensitizing effects while exhibiting little to no side effects and thus represent a new potential class of therapeutics for the treatment of T2DM. Partial agonists have been found to not only display differences in transcriptional and cellular outcomes, but also act through distinct structural and dynamic mechanisms within the ligand binding cavity compared to full agonists.
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spelling doaj-art-d87a39095aaf4064a7a3e0f7e215bc812025-02-03T06:12:41ZengWileyPPAR Research1687-47571687-47652015-01-01201510.1155/2015/816856816856Review of the Structural and Dynamic Mechanisms of PPARγ Partial AgonismAlice J. Kroker0John B. Bruning1School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, AustraliaSchool of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, AustraliaPPARγ (peroxisome proliferator activated receptor γ) is a ligand activated transcription factor of the nuclear receptor superfamily that controls the expression of a variety of genes involved in fatty acid metabolism, adipogenesis, and insulin sensitivity. While endogenous ligands of PPARγ include fatty acids and eicosanoids, synthetic full agonists of the receptor, including members of the thiazolidinedione (TZD) class, have been widely prescribed for the treatment of type II diabetes mellitus (T2DM). Unfortunately, the use of full agonists has been hampered by harsh side effects with some removed from the market in many countries. In contrast, partial agonists of PPARγ have been shown to retain favourable insulin sensitizing effects while exhibiting little to no side effects and thus represent a new potential class of therapeutics for the treatment of T2DM. Partial agonists have been found to not only display differences in transcriptional and cellular outcomes, but also act through distinct structural and dynamic mechanisms within the ligand binding cavity compared to full agonists.http://dx.doi.org/10.1155/2015/816856
spellingShingle Alice J. Kroker
John B. Bruning
Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism
PPAR Research
title Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism
title_full Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism
title_fullStr Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism
title_full_unstemmed Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism
title_short Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism
title_sort review of the structural and dynamic mechanisms of pparγ partial agonism
url http://dx.doi.org/10.1155/2015/816856
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