PPAR dual agonists: Are they opening Pandora's box?

被引:158
作者
Balakumar, Pitchal [1 ]
Rose, Madhankumar
Ganti, Subrahmanya S.
Krishan, Pawan
Singh, Manjeet
机构
[1] Punjabi Univ, Dept Pharmaceut Sci & Drug Res, Cardiovasc Pharmacol Div, Patiala 147002, Punjab, India
[2] ISF Inst Pharmaceut Sci & Drug Res, Moga, Punjab, India
关键词
PPAR dual agonists; diabetic cardiovascular complications; PPAR pan agonists; PROLIFERATOR-ACTIVATED-RECEPTOR; PHYSIOLOGICAL CARDIAC-HYPERTROPHY; PHENYLPROPANOIC ACID-DERIVATIVES; ENDOTHELIAL-CELL ACTIVATION; CORONARY-ARTERY-DISEASE; GAMMA-AGONIST; INSULIN-RESISTANCE; TNF-ALPHA; KAPPA-B; CARDIOVASCULAR-DISEASE;
D O I
10.1016/j.phrs.2007.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiovascular disorders are the major cause of mortality in patients of diabetes mellitus. Peroxisome proliferator activated receptors (PPARs) are ligand-activated transcription factors of nuclear hormone receptor superfamily comprising of three subtypes such as PPAR alpha, PPAR-gamma and PPAR delta/beta. Activation of PPARa reduces triglycerides and involves in regulation of energy homeostasis. Activation of PPAR gamma causes insulin sensitization and enhances glucose metabolism, whereas activation of PPAR delta enhances fatty acid metabolism. Current therapeutic strategies available for the treatment of diabetes do not inhibit the associated secondary cardiovascular complications. Hence, the development of multimodal drugs which can reduce hyperglycemia and concomitantly inhibit the progression of secondary cardiovascular complications may offer valuable therapeutic option. Several basic and clinical studies have exemplified the beneficial effects of PPAR alpha and PPAR gamma ligands in preventing the cardiovascular risks. The PPAR alpha/gamma dual agonists are developed to increase insulin sensitivity and Simultaneously prevent diabetic cardiovascular complications. Such compounds are under clinical trials and proposed for treatment of Type II diabetes with secondary cardiovascular complications. However, PPAR alpha/gamma dual agonists such as muraglitazar, tesaglitazar and ragaglitazar have been noted to produce several cardiovascular risks and carcinogenicity, which raised number of questions about the clinical applications of dual agonists in diabetes and its associated complications. The ongoing basic studies have elucidated the cardio protective role of PPAR delta. Therefore, further studies are on the track to develop PPAR alpha/delta and PPAR gamma/delta dual agonists and PPAR alpha/gamma/delta pan agonists for the treatment of diabetic cardiovascular complications. The present review critically analyzes the protective and detrimental effect of PPAR agonists in diabetic cardiovascular complications. Moreover, the newly developed PPAR alpha/delta and PPAR gamma/delta dual agonists and PPAR alpha/gamma/delta pan agonists have also been discussed which may open a new vista in the management of diabetic cardiovascular complications in near future. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:91 / 98
页数:8
相关论文
共 96 条
[1]   Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-α activator [J].
Aasum, E ;
Belke, DD ;
Severson, DL ;
Riemersma, RA ;
Cooper, M ;
Andreassen, M ;
Larsen, TS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (03) :H949-H957
[2]   Halofenate is a selective peroxisome proliferator-activated receptor γ modulator with antidiabetic activity [J].
Allen, Tamara ;
Zhang, Fang ;
Moodie, Shonna A. ;
Clemens, L. Edward ;
Smith, Aaron ;
Gregoire, Francine ;
Bell, Andrea ;
Muscat, George E. O. ;
Gustafson, Thomas A. .
DIABETES, 2006, 55 (09) :2523-2533
[3]  
[Anonymous], CARDIOVASC DIABETOL
[4]   Possible role of poly (ADP-ribose) polymerase in pathological and physiological cardiac hypertrophy [J].
Balakumar, P. ;
Singh, M. .
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 2006, 28 (10) :683-689
[5]  
Balakumar P., 2006, INT J PHARMACEUT, V2, P543
[6]   Differential role of Rho-kinase in pathological and physiological cardiac hypertrophy in rats [J].
Balakumar, Pitchai ;
Singh, Manjeet .
PHARMACOLOGY, 2006, 78 (02) :91-97
[7]   Anti-tumour necrosis factor-α therapy in heart failure:: Future directions [J].
Balakumar, Pitchai ;
Singh, Manjeet .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2006, 99 (06) :391-397
[8]   The possible role of caspase-3 in pathological and physiological cardiac hypertrophy in rats [J].
Balakumar, Pitchai ;
Singh, Manjeet .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2006, 99 (06) :418-424
[9]   PPARδ:: a dagger in the heart of the metabolic syndrome [J].
Barish, GD ;
Narkar, VA ;
Evans, RM .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (03) :590-597
[10]   PPAR-γ inhibits ANG II-induced cell growth via SHIP2 and 4E-BP1 [J].
Benkirane, K ;
Amiri, F ;
Diep, QN ;
El Mabrouk, M ;
Schiffrin, EL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2006, 290 (01) :H390-H397