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Cyclooxygenases and 5-lipoxygenase in Alzheimer's disease
Authors:Hari Manev  Hu ChenSvetlana Dzitoyeva  Radmila Manev
Affiliation:
  • Department of Psychiatry, University of Illinois at Chicago, Chicago, Illinois, USA
  • 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.
    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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