Literature DB >> 18221086

Role of PPAR in cardiovascular diseases.

Saibal Kumar Das1, Ranjan Chakrabarti.   

Abstract

Cardiovascular disease (CVD) is the most critical global health threat, which contributes more than one third of global morbidity. CVD includes heart disease, vascular disease, atherosclerosis, stroke and hypertension. The most important independent risk factors for CVD include dyslipidemia along with hypertension, obesity, sedentary lifestyle, diabetes and chronic inflammation. These factors are directly regulated by diet, metabolism and physical activity. Diets rich in fat and carbohydrate coupled to sedentary lifestyles have contributed to the increase in dyslipidemia, type 2 diabetes, obesity and CVD in the world. Discovery of Peroxisome Proliferator Activated Receptors (PPARs) as a key regulator of metabolic pathways has led to significant insight into the mechanisms regulating these processes. Three PPAR subtypes, encoded by distinct genes, are designated as PPAR-alpha, PPAR-delta (also know as beta) and PPAR-gamma. PPARs act as nutritional sensors that regulate a variety of homeostatic functions including metabolism, inflammation and development. PPAR-alpha is the main metabolic regulator for catabolism whereas PPAR-gamma regulates anabolism or storage. PPARs are expressed in the cardiovascular system such as endothelial cells, vascular smooth muscle cells and monocytes/macrophages. It has been shown that they play an important role in the modulation of inflammatory, fibrotic and hypertrophic responses. In 1997, a Glaxo patent described that Troglitazone (first PPAR-gamma ligand to reach market) reduced TNF-induced VCAM1 expression in HUVECs indicating the potential benefit in atherosclerosis. A series of patents from Eli Lilly and Dr. Reddy's Laboratories Ltd. between 1999 and 2005 described a variety of PPAR-alpha and -alpha,gamma dual ligands in a number of patents having glucose, triglyceride, cholesterol lowering, HDL elevating and body weight reducing activity. Patents from Metabolex and Tularik in 2001 and 2002 described the beneficial effects of SPPARM molecules for insulin resistance and diabetes, without showing concern on PPAR-gamma related side effects such as edema and body weight. GSK and Takeda described the potential effects of PPAR-delta modulators during 2001 to 2004 in few patents. Several clinical and preclinical studies have demonstrated the beneficial effects of PPAR ligands on various cardiovascular risk factors. This review intends to capture some of the key studies in this area as is described in some recent patents and literature.

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Year:  2006        PMID: 18221086     DOI: 10.2174/157489006777442441

Source DB:  PubMed          Journal:  Recent Pat Cardiovasc Drug Discov


  16 in total

Review 1.  Epigenetic programming and risk: the birthplace of cardiovascular disease?

Authors:  Maria Cristina Vinci; Gianluca Polvani; Maurizio Pesce
Journal:  Stem Cell Rev Rep       Date:  2013-06       Impact factor: 5.739

2.  Suppression of PPARγ through MKRN1-mediated ubiquitination and degradation prevents adipocyte differentiation.

Authors:  J-H Kim; K W Park; E-W Lee; W-S Jang; J Seo; S Shin; K-A Hwang; J Song
Journal:  Cell Death Differ       Date:  2013-12-13       Impact factor: 15.828

3.  The effects of PPARγ on the regulation of the TOMM40-APOE-C1 genes cluster.

Authors:  Shobana Subramanian; William K Gottschalk; So Young Kim; Allen D Roses; Ornit Chiba-Falek
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2017-01-06       Impact factor: 5.187

Review 4.  Is there a role for the incretin system in blood pressure regulation?

Authors:  Akhilesh Rao; Ravi Nistala
Journal:  Curr Hypertens Rep       Date:  2014-03       Impact factor: 5.369

Review 5.  Epigenetic modifications: basic mechanisms and role in cardiovascular disease.

Authors:  Diane E Handy; Rita Castro; Joseph Loscalzo
Journal:  Circulation       Date:  2011-05-17       Impact factor: 29.690

6.  T33, a novel peroxisome proliferator-activated receptor γ/α agonist, exerts neuroprotective action via its anti-inflammatory activities.

Authors:  Ying Wang; Yu-she Yang; Xi-can Tang; Hai-yan Zhang
Journal:  Acta Pharmacol Sin       Date:  2011-08-01       Impact factor: 6.150

7.  Up-regulation of peroxisome proliferator-activated receptor gamma in radiation-induced heart injury in rats.

Authors:  Song Gao; Rong Wu; Yuecan Zeng
Journal:  Radiat Environ Biophys       Date:  2011-10-14       Impact factor: 1.925

8.  Bone marrow mesenchymal stem cell transplantation improves radiation-induced heart injury through DNA damage repair in rat model.

Authors:  Song Gao; Zhiying Zhao; Rong Wu; Yuecan Zeng; Zhenyong Zhang; Jianing Miao; Zhengwei Yuan
Journal:  Radiat Environ Biophys       Date:  2016-12-26       Impact factor: 1.925

9.  Intensive Atorvastatin Therapy Attenuates the Inflammatory Responses in Monocytes of Patients with Unstable Angina Undergoing Percutaneous Coronary Intervention via Peroxisome Proliferator-Activated Receptor γ Activation.

Authors:  Jing Yang; Changqing Liu; Linxia Zhang; Yanhui Liu; Aihua Guo; Huiwu Shi; Xiaoxia Liu; Ying Cheng
Journal:  Inflammation       Date:  2015-08       Impact factor: 4.092

Review 10.  Peroxisome proliferator-activated receptors for hypertension.

Authors:  Daisuke Usuda; Tsugiyasu Kanda
Journal:  World J Cardiol       Date:  2014-08-26
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