Chronic neuroinflammation in rats reproduces components of the neurobiology of Alzheimer's disease

Brain Res. 1998 Jan 12;780(2):294-303. doi: 10.1016/s0006-8993(97)01215-8.

Abstract

Inflammatory processes may play a critical role in the pathogenesis of the degenerative changes and cognitive impairments associated with Alzheimer's disease (AD). In the present study, lipopolysaccharide (LPS) from the cell wall of gram-negative bacteria was used to produce chronic, global inflammation within the brain of young rats. Chronic infusion of LPS (0.25 microgram/h) into the 4th ventricle for four weeks produced (1) an increase in the number of glial fibrillary acidic protein-positive activated astrocytes and OX-6-positive reactive microglia distributed throughout the brain, with the greatest increase occurring within the temporal lobe, particularly the hippocampus, (2) an induction in interleukin-1 beta, tumor necrosis factor-alpha and beta-amyloid precursor protein mRNA levels within the basal forebrain region and hippocampus, (3) the degeneration of hippocampal CA3 pyramidal neurons, and (4) a significant impairment in spatial memory as determined by decreased spontaneous alternation behavior on a T-maze.

Publication types

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

MeSH terms

  • Alzheimer Disease / immunology*
  • Alzheimer Disease / metabolism
  • Amyloid beta-Protein Precursor / genetics
  • Animals
  • Astrocytes / metabolism
  • Choline O-Acetyltransferase / genetics
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Expression Regulation, Enzymologic / immunology
  • Glial Fibrillary Acidic Protein / genetics
  • Glutamate Decarboxylase / genetics
  • Interleukin-1 / genetics
  • Interleukin-6 / genetics
  • Lipopolysaccharides
  • Maze Learning
  • Microglia / metabolism
  • Neuritis / chemically induced
  • Neuritis / immunology*
  • Neuritis / metabolism
  • Neurons / chemistry
  • Neurons / enzymology
  • Prosencephalon / immunology
  • Prosencephalon / metabolism
  • RNA, Messenger / analysis
  • Rats
  • Rats, Inbred F344
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Amyloid beta-Protein Precursor
  • Glial Fibrillary Acidic Protein
  • Interleukin-1
  • Interleukin-6
  • Lipopolysaccharides
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Choline O-Acetyltransferase
  • Glutamate Decarboxylase