Influence of LPS-induced neuroinflammation on acetylcholinesterase activity in rat brain

J Neuroimmunol. 2008 Dec 15;205(1-2):51-6. doi: 10.1016/j.jneuroim.2008.08.015. Epub 2008 Oct 5.

Abstract

In the present study, neuroinflammation was induced by bilateral intracerebroventricular (ICV) administration of Lipopolysaccharide (LPS). Proinflammatory cytokines (TNF-alpha and IL-1beta), acetylcholinesterase (AChE) activity, malondialdehyde (MDA) and reduced glutathione (GSH) were studied as markers for neuroinflammation, cholinergic activity and oxidative stress respectively in different brain regions at different time points after LPS injection. LPS produced increase in proinflammatory cytokines, MDA and the decrease in level of GSH at 24 h indicating a state of inflammation in brain regions, which was significantly blocked by Ibuprofen, a non steroidal anti-inflammatory drug. Enhanced AChE activity with these inflammatory markers after LPS administration indicates a possible relationship between neuroinflammation and cholinergic system during the development of neurodegenerative diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Brain / drug effects
  • Brain / enzymology*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Encephalitis / chemically induced*
  • Encephalitis / drug therapy
  • Encephalitis / enzymology*
  • Enzyme-Linked Immunosorbent Assay / methods
  • Glutathione / metabolism
  • Ibuprofen / pharmacology
  • Ibuprofen / therapeutic use
  • Injections, Intraventricular / methods
  • Lipopolysaccharides / administration & dosage
  • Lipopolysaccharides / toxicity*
  • Male
  • Malondialdehyde / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Lipopolysaccharides
  • Malondialdehyde
  • Acetylcholinesterase
  • Glutathione
  • Ibuprofen