Antiinflammatory properties of PPARγ agonists following ischemia

被引:45
作者
Sundararajan, S
Landreth, GE
机构
[1] Univ Hosp Cleveland, Dept Neurol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
关键词
D O I
10.1358/dnp.2004.17.4.829049
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ischemic disease is a leading cause of death and disability worldwide, and its incidence is expected to increase as the population ages. One population at particularly high risk of developing ischemia is patients with diabetes. Type 2 diabetes is associated with a marked increase in atherosclerosis, stroke and heart attack. Furthermore, the outcome following stroke and heart attack in diabetics is worse than in nondiabetic patients. In recent years, peroxisome proliferator-activated receptor (PPAR) agonists have been found to have potent antiinflammatory actions and have emerged as potential therapies for atherosclerosis and ischemia. The use of these agents is particularly attractive, since two PPARgamma agonists, pioglitazone (Actos(TM)) and rosiglitazone (Avandia(TM)), are already used chronically to treat diabetes. In this article we review the role of inflammation in ischemic disease and the biology of PPARs, and summarize the evidence that PPARgamma ligands suppress inflammation with an emphasis on atherosclerosis, and cerebral and myocardial ischemia. (C) 2004 Prous Science. Ail rights reserved.
引用
收藏
页码:229 / 236
页数:8
相关论文
共 97 条
[1]  
AIZAWA Y, 2001, CIRCULATION, V97, P2307
[2]  
Alleva DG, 2002, J LEUKOCYTE BIOL, V71, P677
[3]   Neuroprotective effects of PPAR-γ agonists against oxidative insults in HT-22 cells [J].
Aoun, P ;
Watson, DG ;
Simpkins, JW .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 472 (1-2) :65-71
[4]   An anti-CD18 antibody limits infarct size and preserves left ventricular function in dogs with ischemia and 48-hour reperfusion [J].
Arai, M ;
Lefer, DJ ;
So, T ;
DiPaula, A ;
Aversano, T ;
Becker, LC .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 27 (05) :1278-1285
[5]  
ARONOWSKI J, 2002, SOC NEUR M NOV 2 7 O
[6]  
BARONE F, 2000, STROKE, V28, P1233
[7]   Inflammatory mediators and stroke: New opportunities for novel therapeutics [J].
Barone, FC ;
Feuerstein, GZ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (08) :819-834
[8]   Protective action of the peroxisome proliferator-activated receptor-γ agonist pioglitazone in a mouse model of Parkinson's disease [J].
Breidert, T ;
Callebert, J ;
Heneka, MT ;
Landreth, G ;
Launay, JM ;
Hirsch, EC .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (03) :615-624
[9]   Inhibition of IκB kinase and IκB phosphorylation by 15-deoxy-Δ12,14-prostaglandin J2 in activated murine macrophages [J].
Castrillo, A ;
Díaz-Guerra, MJM ;
Hortelano, S ;
Martín-Sanz, P ;
Boscá, L .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1692-1698
[10]   A PPARγ-LXR-ABCA1 pathway in macrophages is involved in cholesterol efflux and atherogenesis [J].
Chawla, A ;
Boisvert, WA ;
Lee, CH ;
Laffitte, BA ;
Barak, Y ;
Joseph, SB ;
Liao, D ;
Nagy, L ;
Edwards, PA ;
Curtiss, LK ;
Evans, RM ;
Tontonoz, P .
MOLECULAR CELL, 2001, 7 (01) :161-171