Peroxisome proliferator-activated receptor-alpha (PPARα): At the crossroads of obesity, diabetes and cardiovascular disease

被引:198
作者
Fruchart, Jean-Charles [1 ]
机构
[1] Univ Lille 2, Fac Med Lille, INSERM, Lab J&K,UR 545, F-59045 Lille, France
关键词
Peroxisome proliferator-activated receptor alpha; Lipoprotein metabolism; Inflammation; Vascular function; Cardiovascular; Microvascular; SECONDARY PREVENTION; INSULIN-RESISTANCE; RISK-FACTORS; KAPPA-B; FENOFIBRATE; GAMMA; CHOLESTEROL; EXPRESSION; GEMFIBROZIL; MECHANISM;
D O I
10.1016/j.atherosclerosis.2009.03.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular disease is the leading cause of morbidity and mortality world-wide. The burden of disease is also increasing as a result of the global epidemics of diabetes and obesity. Peroxisome proliferator-activated receptor a (PPAR(x), a member of this nuclear receptor family, has emerged as an important player in this scenario, with evidence supporting a central co-ordinated role in the regulation of fatty acid oxidation, lipid and lipoprotein metabolism and inflammatory and vascular responses, all of which would be predicted to reduce atherosclerotic risk. Additionally, the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study has indicated the possibility of preventive effects in diabetes-related microvascular complications, although the mechanisms of these effects warrant further study. The multimodal pharmacological profile of PPAR alpha has prompted development of selective PPAR modulators (SPPARMs) to maximise therapeutic potential. It is anticipated that PPARa will continue to have important clinical application in addressing the major challenge of cardiometabolic risk associated with type 2 diabetes, obesity and metabolic syndrome. (C) 2009 Published by Elsevier Ireland Ltd.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 66 条
[1]  
[Anonymous], US OBESITY TRENDS 19
[2]  
[Anonymous], DIABETES PREVALENCE
[3]   HDL cholesterol, very low levels of LDL cholesterol, and cardiovascular events [J].
Barter, Philip ;
Gotto, Antonio M. ;
LaRosa, John C. ;
Maroni, Jaman ;
Szarek, Michael ;
Grundy, Scott M. ;
Kastelein, John J. P. ;
Bittner, Vera ;
Fruchart, Jean-Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (13) :1301-1310
[4]  
Bloomgarden Zachary T, 2005, Diabetes Care, V28, P2073, DOI 10.2337/diacare.28.8.2073
[5]   CLA-1/SR-BI is expressed in atherosclerotic lesion macrophages and regulated by activators of peroxisome proliferator-activated receptors [J].
Chinetti, G ;
Gbaguidi, FG ;
Griglio, S ;
Mallat, Z ;
Antonucci, M ;
Poulain, P ;
Chapman, J ;
Fruchart, JC ;
Tedgui, A ;
Najib-Fruchart, J ;
Staels, B .
CIRCULATION, 2000, 101 (20) :2411-2417
[6]   Peroxisome proliferator-activated receptor α reduces cholesterol esterification in macrophages [J].
Chinetti, G ;
Lestavel, S ;
Fruchart, JC ;
Clavey, V ;
Staels, B .
CIRCULATION RESEARCH, 2003, 92 (02) :212-217
[7]   Activation of proliferator-activated receptors α and γ induces apoptosis of human monocyte-derived macrophages [J].
Chinetti, G ;
Griglio, S ;
Antonucci, M ;
Torra, IP ;
Delerive, P ;
Majd, Z ;
Fruchart, JC ;
Chapman, J ;
Najib, J ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :25573-25580
[8]   PPAR-α and PPAR-γ activators induce cholesterol removal from human macrophage foam cells through stimulation of the ABCA1 pathway [J].
Chinetti, G ;
Lestavel, S ;
Bocher, V ;
Remaley, AT ;
Neve, B ;
Torra, IP ;
Teissier, E ;
Minnich, A ;
Jaye, M ;
Duverger, N ;
Brewer, HB ;
Fruchart, JC ;
Clavey, V ;
Staels, B .
NATURE MEDICINE, 2001, 7 (01) :53-58
[9]   Peroxisome proliferator-activated receptor α controls cellular cholesterol trafficking in macrophages [J].
Chinetti-Gbaguidi, G ;
Rigamonti, E ;
Helin, L ;
Mutka, AL ;
Lepore, M ;
Fruchart, JC ;
Clavey, V ;
Ikonen, E ;
Lestavel, S ;
Staels, B .
JOURNAL OF LIPID RESEARCH, 2005, 46 (12) :2717-2725
[10]   Role of the PPAR family of nuclear receptors in the regulation of metabolic and cardiovascular homeostasis: new approaches to therapy [J].
Chinetti-Gbaguidi, G ;
Fruchart, JC ;
Staels, B .
CURRENT OPINION IN PHARMACOLOGY, 2005, 5 (02) :177-183