Beta-amyloid-induced inflammation and cholinergic hypofunction in the rat brain in vivo: involvement of the p38MAPK pathway

Neurobiol Dis. 2002 Nov;11(2):257-74. doi: 10.1006/nbdi.2002.0538.

Abstract

Injection into the nucleus basalis of the rat of preaggregated Abeta(1-42) produced a congophylic deposit and microglial and astrocyte activation and infiltration and caused a strong inflammatory reaction characterized by IL-1beta production, increased inducible cyclooxygenase (COX-2), and inducible nitric oxide synthase (iNOS) expression. Many phospho-p38MAPK-positive cells were observed around the deposit at 7 days after Abeta injection. Phospho-p38MAPK colocalized with activated microglial cells, but not astrocytes. The inflammatory reaction was accompanied by cholinergic hypofunction. We investigated the protective effect of the selective COX-2 inhibitor rofecoxib in attenuating the inflammatory response and neurodegeneration evoked by Abeta(1-42). Rofecoxib (3 mg/kg/day, 7 days) reduced microglia and astrocyte activation, iNOS induction, and p38MAPK activation to control levels. Cholinergic hypofunction was also significantly attenuated by treatment with rofecoxib. We show here for the first time in vivo the pivotal role played by the p38MAPK microglial signal transduction pathway in the inflammatory response to the Abeta(1-42) deposit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism
  • Alzheimer Disease / enzymology*
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology
  • Amyloid beta-Peptides / metabolism*
  • Amyloid beta-Peptides / pharmacology
  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism
  • Basal Nucleus of Meynert / drug effects
  • Basal Nucleus of Meynert / enzymology*
  • Basal Nucleus of Meynert / pathology
  • Choline O-Acetyltransferase / drug effects
  • Choline O-Acetyltransferase / metabolism
  • Cholinergic Fibers / drug effects
  • Cholinergic Fibers / enzymology*
  • Cholinergic Fibers / pathology
  • Cyclooxygenase 2
  • Down-Regulation / drug effects
  • Down-Regulation / physiology
  • Encephalitis / chemically induced
  • Encephalitis / enzymology*
  • Encephalitis / physiopathology
  • Gliosis / chemically induced
  • Immunohistochemistry
  • Interleukin-1 / metabolism
  • Isoenzymes / drug effects
  • Isoenzymes / metabolism
  • MAP Kinase Signaling System / drug effects
  • MAP Kinase Signaling System / physiology
  • Male
  • Microglia / drug effects
  • Microglia / metabolism
  • Mitogen-Activated Protein Kinases / drug effects
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neurons / drug effects
  • Neurons / enzymology*
  • Neurons / pathology
  • Nitric Oxide Synthase / drug effects
  • Nitric Oxide Synthase / metabolism
  • Peptide Fragments / metabolism*
  • Peptide Fragments / pharmacology
  • Prostaglandin-Endoperoxide Synthases / drug effects
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Rats
  • Rats, Wistar
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Amyloid beta-Peptides
  • Interleukin-1
  • Isoenzymes
  • Peptide Fragments
  • amyloid beta-protein (1-42)
  • Nitric Oxide Synthase
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Choline O-Acetyltransferase
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Acetylcholine