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Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis

Peroxisome proliferator-activated receptor-γ (PPARγ) is a ligand-activated transcription factor belonging to the nuclear receptor superfamily, which plays a central role in regulating lipid and glucose metabolism. However, accumulating evidence demonstrates that PPARγ agonists have potential to redu...

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Detalles Bibliográficos
Autores principales: Liu, Huang-Jun, Liao, Hai-Han, Yang, Zheng, Tang, Qi-Zhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880703/
https://www.ncbi.nlm.nih.gov/pubmed/27293418
http://dx.doi.org/10.1155/2016/2198645
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author Liu, Huang-Jun
Liao, Hai-Han
Yang, Zheng
Tang, Qi-Zhu
author_facet Liu, Huang-Jun
Liao, Hai-Han
Yang, Zheng
Tang, Qi-Zhu
author_sort Liu, Huang-Jun
collection PubMed
description Peroxisome proliferator-activated receptor-γ (PPARγ) is a ligand-activated transcription factor belonging to the nuclear receptor superfamily, which plays a central role in regulating lipid and glucose metabolism. However, accumulating evidence demonstrates that PPARγ agonists have potential to reduce inflammation, influence the balance of immune cells, suppress oxidative stress, and improve endothelial function, which are all involved in the cellular and molecular mechanisms of cardiac fibrosis. Thus, in this review we discuss the role of PPARγ in various cardiovascular conditions associated with cardiac fibrosis, including diabetes mellitus, hypertension, myocardial infarction, heart failure, ischemia/reperfusion injury, atrial fibrillation, and several other cardiovascular disease (CVD) conditions, and summarize the developmental status of PPARγ agonists for the clinical management of CVD.
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spelling pubmed-48807032016-06-12 Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis Liu, Huang-Jun Liao, Hai-Han Yang, Zheng Tang, Qi-Zhu PPAR Res Review Article Peroxisome proliferator-activated receptor-γ (PPARγ) is a ligand-activated transcription factor belonging to the nuclear receptor superfamily, which plays a central role in regulating lipid and glucose metabolism. However, accumulating evidence demonstrates that PPARγ agonists have potential to reduce inflammation, influence the balance of immune cells, suppress oxidative stress, and improve endothelial function, which are all involved in the cellular and molecular mechanisms of cardiac fibrosis. Thus, in this review we discuss the role of PPARγ in various cardiovascular conditions associated with cardiac fibrosis, including diabetes mellitus, hypertension, myocardial infarction, heart failure, ischemia/reperfusion injury, atrial fibrillation, and several other cardiovascular disease (CVD) conditions, and summarize the developmental status of PPARγ agonists for the clinical management of CVD. Hindawi Publishing Corporation 2016 2016-05-12 /pmc/articles/PMC4880703/ /pubmed/27293418 http://dx.doi.org/10.1155/2016/2198645 Text en Copyright © 2016 Huang-Jun Liu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Liu, Huang-Jun
Liao, Hai-Han
Yang, Zheng
Tang, Qi-Zhu
Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis
title Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis
title_full Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis
title_fullStr Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis
title_full_unstemmed Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis
title_short Peroxisome Proliferator-Activated Receptor-γ Is Critical to Cardiac Fibrosis
title_sort peroxisome proliferator-activated receptor-γ is critical to cardiac fibrosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880703/
https://www.ncbi.nlm.nih.gov/pubmed/27293418
http://dx.doi.org/10.1155/2016/2198645
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