Cyclooxygenases and 5-lipoxygenase in Alzheimer's disease |
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Authors: | Hari Manev Hu ChenSvetlana Dzitoyeva Radmila Manev |
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Affiliation: | Department of Psychiatry, University of Illinois at Chicago, Chicago, Illinois, USA |
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Abstract: | 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. |
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Keywords: | AA, arachidonic acid AD, Alzheimer's disease CNS, central nervous system COXs, cyclooxygenases CysLT1, cysteinyl leukotriene 1 EP, prostaglandin E receptor GPCRs, G protein-coupled receptors 5-LOX, 5-lipoxygenase LTB4, leukotriene B4 LXA4, lipoxin A4 NSAIDs, nonsteroidal anti-inflammatory drugs NSC, neural stem cell PET, positron emission tomography PGE2, prostaglandin E2 PGH2, prostaglandin H2 PPAR, peroxisome proliferator-activated receptor 15R-HETE, (15R)-15-hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid SNPs, single nucleotide polymorphisms |
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