Literature DB >> 15029092

Clinical interest of PPARs ligands.

B Vergès1.   

Abstract

Cardiovascular disease is significantly increased in patients with metabolic syndrome and type 2 diabetes. Several factors such as chronic hyperglycemia, lipId abnormalities, endothelium dysfunction, inflammation, oxIdative stress, increased thrombosis and decreased fibrinolysis are likely to promote cardiovascular events in these patients. Because of positive effects on glucose homeostasis, lipId metabolism, proteins involved in all stages of atherogenesis, endothelium function, inflammation, thrombosis and fibrinolysis, PPARS alpha (fibrates) and PPARs gamma (glitazones) agonists are good candIdates to reduce cardiovascular disease, more precisely in subjects with metabolic syndrome or type 2 diabetes. PPARS alpha agonists (fibrates) are potent hypolipIdemic agents increasing plasma HDL-cholesterol and reducing free fatty acIds, triglycerIdes, LDL-cholesterol and the number of small dense LDL pArticles. Moreover, they reduce vascular inflammation and thrombosis, promote fibrinolysis and inhibit the production of the vasoconstrictor factor, endothelin-1, by the endothelium. They have been shown, in clinical trials, to reduce cardiovascular disease, more particularly in patients displaying lipId abnormalities typical of metabolic syndrome and type 2 diabetes (high triglycerIdes, low HDL-cholesterol). PPARS gamma agonists (glitazones) have not only beneficial effects on glucose homeostasis, by increasing insulin sensitivity and reducing blood glucose level but also on lipId metabolism by elevating plasma HDL-cholesterol, decreasing free fatty acIds and the number of small dense LDL pArticles, and for pioglitazone by reducing plasma triglycerIdes. Furthermore, they diminish vascular inflammation and vasoconstriction, inhibit monocyte chemotaxis, proliferation and migration of smooth muscle cells, in the vascular wall and decrease the production of adhesion molecules and metalloproteinases. PPARs gamma agonists (glitazones) have been shown to reduce the development of atherosclerotic lesions in rats. The potential clinical benefit of PPARs gamma agonists on the reduction of cardiovascular disease, in type 2 diabetic patients, will be specified by the ongoing intervention studies.

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Year:  2004        PMID: 15029092     DOI: 10.1016/s1262-3636(07)70083-6

Source DB:  PubMed          Journal:  Diabetes Metab        ISSN: 1262-3636            Impact factor:   6.041


  17 in total

1.  Single and chronic administration of ciprofibrate or of ciprofibrate-glycinate in male Fischer 344 rats: comparison of the effects on morphological and biochemical parameters in liver and blood.

Authors:  Amelie Lupp; Elke Karge; Manfred Danz; Thomas Deufel; Herbert Oelschläger; Wolfgang Klinger
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2005 Jul-Sep       Impact factor: 2.441

Review 2.  PPAR ligands: potential therapies for metabolic syndrome.

Authors:  Taro E Akiyama; Peter T Meinke; Joel P Berger
Journal:  Curr Diab Rep       Date:  2005-02       Impact factor: 4.810

3.  Coronary microvascular dysfunction in diabetes mellitus: A review.

Authors:  Andrea Picchi; Stefano Capobianco; Tianyi Qiu; Marta Focardi; Xiaoqin Zou; Ji-Min Cao; Cuihua Zhang
Journal:  World J Cardiol       Date:  2010-11-26

4.  The pathophysiology of obesity and its clinical manifestations.

Authors:  Richard N Redinger
Journal:  Gastroenterol Hepatol (N Y)       Date:  2007-11

5.  Airway epithelial cell PPARγ modulates cigarette smoke-induced chemokine expression and emphysema susceptibility in mice.

Authors:  Siva Kumar Solleti; Dawn M Simon; Sorachai Srisuma; Meltem C Arikan; Soumyaroop Bhattacharya; Tirumalai Rangasamy; Kaiser M Bijli; Arshad Rahman; Joseph T Crossno; Steven D Shapiro; Thomas J Mariani
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2015-05-29       Impact factor: 5.464

6.  "If it ain't broke, don't fix it": a commentary on the positive-negative results of the ACCORD Lipid study.

Authors:  Alexander Tenenbaum; Enrique Z Fisman
Journal:  Cardiovasc Diabetol       Date:  2010-06-15       Impact factor: 9.951

7.  Maturation-induces endothelial dysfunction via vascular inflammation in diabetic mice.

Authors:  Cuihua Zhang; Yoonjung Park; Andrea Picchi; Barry J Potter
Journal:  Basic Res Cardiol       Date:  2008-07-03       Impact factor: 17.165

8.  Therapeutic Implications of PPARgamma in Cardiovascular Diseases.

Authors:  Hiroshi Hasegawa; Hiroyuki Takano; Issei Komuro
Journal:  PPAR Res       Date:  2010-08-12       Impact factor: 4.964

Review 9.  The Microvascular and Macrovascular Benefits of Fibrates in Diabetes and the Metabolic Syndrome: A review.

Authors:  Pavan Malur; Arthur Menezes; James J DiNicolantonio; James H O'Keefe; Carl J Lavie
Journal:  Mo Med       Date:  2017 Nov-Dec

10.  Metabolic syndrome in the rural population of wardha, central India: an exploratory factor analysis.

Authors:  Pradeep R Deshmukh; Pranita Kamble; Kalyan Goswami; Neelam Garg
Journal:  Indian J Community Med       Date:  2013-01
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