Downregulation of neuronal cyclooxygenase-2 expression in end stage Alzheimer's disease

Neurobiol Aging. 2001 Nov-Dec;22(6):823-36. doi: 10.1016/s0197-4580(01)00303-7.

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) appear to delay the onset of Alzheimer's disease (AD). NSAIDs inhibit cyclooxygenase (COX), of which two isoforms exist. We report decreased neuronal COX-2 expression in AD subjects relative to nondemented controls using qualitative analysis of COX-2 immunoreactivity and quantification of COX-2 positive neurons in different hippocampal subfields. These changes also occurred in subjects with other dementia and thus may not be disease specific. The proportion of COX-2 positive neurons decreased in subjects with clinical dementia rating (CDR) 5 but not CDR 4, suggesting that this was a late event in the course of the disease. Furthermore, COX-2 was not preferentially associated with paired helical filament immunoreactivity, a marker of neuronal pathology. COX-2 immunoreactivity was also observed in astrocytes and cerebrovasculature. Indeed, the density of COX-2 immunopositive astrocytes was increased in AD temporal cortex. Based on our findings, it is unlikely that neuronal COX-2 contributes to pathology in end stage AD; however, COX-2 in other cell types may participate in the inflammation-related response associated with the disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aging / pathology
  • Alzheimer Disease / enzymology*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology
  • Antibody Specificity
  • Astrocytes / pathology
  • Autopsy
  • Blotting, Western
  • Brain / enzymology
  • Brain / pathology
  • Cerebral Cortex / enzymology
  • Cerebral Cortex / pathology
  • Cyclooxygenase 2
  • Down-Regulation / genetics*
  • Hippocampus / enzymology
  • Hippocampus / pathology
  • Humans
  • Immunohistochemistry
  • Isoenzymes / biosynthesis*
  • Isoenzymes / genetics
  • Membrane Proteins
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / pathology
  • Neuroglia / enzymology
  • Neurons / enzymology*
  • Neurons / pathology
  • Postmortem Changes
  • Prostaglandin-Endoperoxide Synthases / biosynthesis*
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Sex Characteristics
  • tau Proteins / metabolism

Substances

  • Isoenzymes
  • Membrane Proteins
  • tau Proteins
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases