Hippocampal kindling epileptogenesis upregulates neuronal cyclooxygenase-2 expression in neocortex

Exp Neurol. 2003 Feb;179(2):167-75. doi: 10.1016/s0014-4886(02)00019-5.

Abstract

Recurrent and spontaneous seizures in epilepsy result from poorly defined cell signaling aberrations thought to include synaptic and extracellular matrix remodeling. Here we have used a rat hippocampal kindling model to study cyclooxygenase-2 (COX-2) gene expression in epileptogenesis. COX-2, encoded in an early-response gene, increases in a synaptic activity-dependent fashion and also during kainic acid-induced hippocampal damage. We found that during kindling, COX-2 induction occurred initially only in hippocampal neurons, and then spread to neocortical neurons. When rats were rekindled 34 days later, this spreading of COX-2 expression persisted. Induction of hippocampal and neocortical cytosolic phospholipase A(2) (cPLA(2)), an enzyme that catalyzes the synthesis of COX-2 substrate arachidonic acid (AA), occurred after 4 days of stimulation during kindling and rekindling. Moreover the COX-2 selective inhibitor nimesulide attenuated kindling development. We conclude that neuronal COX-2 gene induction and cPLA(2) activation are key signaling events in epileptogenesis.

Publication types

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

MeSH terms

  • Animals
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / pharmacology
  • Cytosol / enzymology
  • Disease Models, Animal
  • Enzyme Induction
  • Epilepsy / drug therapy
  • Epilepsy / pathology
  • Epilepsy / physiopathology*
  • Hippocampus / pathology
  • Hippocampus / physiopathology*
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Kindling, Neurologic / metabolism*
  • Male
  • Neocortex / enzymology*
  • Neocortex / pathology
  • Neurons / enzymology
  • Neurons / pathology
  • Phospholipases A / metabolism
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Sulfonamides / pharmacology
  • Up-Regulation

Substances

  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • RNA, Messenger
  • Sulfonamides
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Phospholipases A
  • nimesulide