Molecular targets of non-steroidal anti-inflammatory drugs in neurodegenerative diseases

被引:91
作者
Lleo, A.
Galea, E.
Sastre, M. [1 ]
机构
[1] Hosp Santa Creu & Sant Pau, Dept Neurol, Barcelona 08025, Spain
[2] Univ Autonoma Barcelona, Inst Neurosci, E-08193 Barcelona, Spain
[3] ICREA, Catalonian Inst Adv Studies, Barcelona 08193, Spain
[4] Univ Bonn, Dept Neurol, D-53127 Bonn, Germany
关键词
NSAIDs; PPAR gamma; Alzheimer's disease; inflammation; neurodegeneration;
D O I
10.1007/s00018-007-6516-1
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
During the last decade, interest has grown in the beneficial effects of non-steroidal anti-inflammatory drugs (NSAIDs) in neurodegeneration, particularly in pathologies such as Alzheimer's (AD) and Parkinson's (PD) disease. Evidence from epidemiological studies has indicated a decreased risk for AD and PD in patients with a history of chronic NSAID use. However, clinical trials with NSAIDs in AD patients have yielded conflicting results, suggesting that these drugs may be beneficial only when used as preventive therapy or in early stages of the disease. NSAIDs may also have salutary effects in other neurodegenerative diseases with an inflammatory component, such as multiple sclerosis and amyotrophic lateral sclerosis. In this review we analyze the molecular (cyclooxygenases, secretases, NF-kappa B, PPAR, or Rho-GTPasas) and cellular (neurons, microglia, astrocytes or endothelial cells) targets of NSAIDs that may mediate the therapeutic function of these drugs in neurodegeneration.
引用
收藏
页码:1403 / 1418
页数:16
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