Increased expression of mRNA encoding ferritin heavy chain in brain structures of a rat model of absence epilepsy

Exp Neurol. 2000 Mar;162(1):112-20. doi: 10.1006/exnr.2000.7303.

Abstract

Differential mRNA display was carried out to find genes that are differentially regulated in the brain of a rat strain with absence epilepsy, the genetic absence epilepsy rats from Strasbourg (GAERS). Among the 32 differentially displayed cDNA fragments actually cloned and sequenced, one shows 100% identity with the rat heavy chain ferritin (H-ferritin) mRNA. Northern blot analysis confirmed the up-regulation of the H-ferritin mRNA. Using dot blotting, a 40% increase in expression was reported in the subcortical forebrain of the adult GAERS, while cortex, brain stem, and cerebellum appeared unmodified. This change was not observed in the brain of 25-day-old rats, an age at which the epileptic phenotype is not present. By in situ hybridization, the enhanced expression was localized in the hippocampus. The increase in mRNA encoding H-ferritin was not immunodetected at the protein level by Western blotting. These results are not apparently related to the neural substrate of SWD or to the distribution of local increase in glucose metabolism previously described in the GAERS. It is hypothesized that the up-regulation of the H-ferritin mRNA is part of a mechanism protecting the hippocampus, a seizure-prone area, against a possible overactivation during absence seizures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Amino Acid Sequence
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Brain Chemistry / genetics*
  • Disease Models, Animal
  • Epilepsy, Absence / genetics*
  • Epilepsy, Absence / physiopathology
  • Ferritins / analysis
  • Ferritins / genetics*
  • Gene Expression Regulation, Developmental / physiology
  • Hippocampus / chemistry
  • Hippocampus / physiology
  • In Situ Hybridization
  • Kindling, Neurologic / physiology
  • Male
  • Molecular Sequence Data
  • Phenotype
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Mutant Strains
  • Rats, Wistar
  • Transcription, Genetic / physiology

Substances

  • RNA, Messenger
  • Ferritins