Cyclooxygenases and 5-lipoxygenase in Alzheimer's disease

被引:62
|
作者
Manev, Hari [1 ]
Chen, Hu [1 ]
Dzitoyeva, Svetlana [1 ]
Manev, Radmila [1 ]
机构
[1] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
来源
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY | 2011年 / 35卷 / 02期
关键词
Alzheimer; Aging; 5-Lipoxygenase; Cyclooxygenase; Lipid; FOCAL CEREBRAL-ISCHEMIA; ANTIINFLAMMATORY DRUGS; RAT HIPPOCAMPUS; LEUKOTRIENE B-4; LIPOXIN A(4); MOUSE MODEL; BRAIN; EXPRESSION; RECEPTOR; DIFFERENTIATION;
D O I
10.1016/j.pnpbp.2010.07.032
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Typically, cyclooxygenases (COXs) and 5-lipoxygenase (5-LOX), enzymes that generate biologically active lipid molecules termed eicosanoids, are considered inflammatory. Hence, their putative role in Alzheimer's disease (AD) has been explored in the framework of possible inflammatory mechanisms of AD pathobiology. More recent data indicate that these enzymes and the biologically active lipid molecules they generate could influence the functioning of the central nervous system and the pathobiology of neurodegenerative disorders such as AD via mechanisms different from classical inflammation. These mechanisms include the cell-specific localization of COXs and 5-LOX in the brain, the type of lipid molecules generated by the activity of these enzymes, the type and the localization of receptors selective for a type of lipid molecule, and the putative interactions of the COXs and 5-LOX pathways with intracellular components relevant for AD such as the gamma-secretase complex. Considering the importance of these multiple and not necessarily inflammatory mechanisms may help us delineate the exact nature of the involvement of the brain COXs and 5-LOX in AD and would reinvigorate the search for novel targets for AD therapy. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:315 / 319
页数:5
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