PPARγ as a therapeutic target in central nervous system diseases

被引:91
作者
Sundararajan, Sophia
Jiang, Qingguang
Heneka, Michael
Landreth, Gary
机构
[1] Case Western Reserve Univ, Sch Med, Alzheimers Res Lab, Dept Neurol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
[3] Univ Munster, Dept Neurol, D-14849 Munster, Germany
关键词
Alzheimer's disease; stroke; multiple sclerosis; Parkinson's disease; amytrophic lateral sclerosis;
D O I
10.1016/j.neuint.2006.03.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diseases of the central nervous system present a challenge for the development of new therapeutic agents. Nuclear receptors are ligand-activated transcription factors that have proven to be valuable targets for development of new drugs owing to their ability to directly regulate gene expression. The nuclear receptor, peroxisome proliferator-activated receptor gamma (PPAR gamma), has been investigated for its action in ameliorating the development and progression of a number of CNS diseases. PPAR gamma agonists exhibit potent anti-inflammatory effects and appear to have direct neuroprotective actions. PPAR gamma agonists have been shown to be efficacious in animal models of Alzheimer's disease, stroke, multiple sclerosis, Parkinson's disease and amyotrophic lateral sclerosis. The availability of FDA-approved agonists of this receptor will facilitate the rapid translation of these findings into clinical trials for a number of CNS diseases. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:136 / 144
页数:9
相关论文
共 85 条
[61]   PPARγ antagonists exacerbate neural antigen-specific Th1 response and experimental allergic encephalomyelitis [J].
Raikwar, HP ;
Muthian, G ;
Rajasingh, J ;
Johnson, C ;
Bright, JJ .
JOURNAL OF NEUROIMMUNOLOGY, 2005, 167 (1-2) :99-107
[62]   INTERLEUKIN-1 RECEPTOR ANTAGONIST INHIBITS ISCHEMIC AND EXCITOTOXIC NEURONAL DAMAGE IN THE RAT [J].
RELTON, JK ;
ROTHWELL, NJ .
BRAIN RESEARCH BULLETIN, 1992, 29 (02) :243-246
[63]   The peroxisome proliferator-activated receptor-γ is a negative regulator of macrophage activation [J].
Ricote, M ;
Li, AC ;
Willson, TM ;
Kelly, CJ ;
Glass, CK .
NATURE, 1998, 391 (6662) :79-82
[64]  
RISNER ME, 2006, PHARMACOGENOM J
[65]   Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IκB kinase [J].
Rossi, A ;
Kapahi, P ;
Natoli, G ;
Takahashi, T ;
Chen, Y ;
Karin, M ;
Santoro, MG .
NATURE, 2000, 403 (6765) :103-108
[66]   PPARγ agonist rosiglitazone improves vascular function and lowers blood pressure in hypertensive transgenic mice [J].
Ryan, MJ ;
Didion, SP ;
Mathur, S ;
Faraci, FM ;
Sigmund, CD .
HYPERTENSION, 2004, 43 (03) :661-666
[67]  
Sastre M, 2003, J NEUROSCI, V23, P9796
[68]   Nonsteroidal anti-inflammatory drugs repress β-secretase gene promoter activity by the activation of PPARγ [J].
Sastre, M ;
Dewachter, I ;
Rossner, S ;
Bogdanovic, N ;
Rosen, E ;
Borghgraef, P ;
Evert, BO ;
Dumitrescu-Ozimek, L ;
Thal, DR ;
Landreth, G ;
Walter, J ;
Klockgether, T ;
van Leuven, F ;
Heneka, MT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (02) :443-448
[69]   Anti-inflammatory and antiproliferative actions of PPAR-γ agonists on T lymphocytes derived from MS patients [J].
Schmidt, S ;
Moric, E ;
Schmidt, M ;
Sastre, M ;
Feinstein, DL ;
Heneka, MT .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 75 (03) :478-485
[70]   The oral antidiabetic pioglitazone protects from neurodegeneration and amyotrophic lateral sclerosis-like symptoms in superoxide dismutase-G93A transgenic mice [J].
Schütz, B ;
Reimann, J ;
Dumitrescu-Ozimek, L ;
Kappes-Horn, K ;
Landreth, GE ;
Schürmann, B ;
Zimmer, A ;
Heneka, MT .
JOURNAL OF NEUROSCIENCE, 2005, 25 (34) :7805-7812