Effect of cortical spreading depression on the levels of mRNA coding for putative neuroprotective proteins in rat brain

Katalin Karikó, Valerie A. Harris, Yolanda Rangel, Monica E. Duvall, Frank A. Welsh

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Previous studies have demonstrated that cortical spreading depression (CSD) induces neuronal tolerance to a subsequent episode of ischemia. The objective of the present investigation was to determine whether CSD alters levels of mRNA coding for putative neuroprotective proteins. Unilateral CSD was evoked in male Wistar rats by applying 2 mol/L KCl over the frontal cortex for 2 hours. After recovery for 0, 2, or 24 hours, levels of several mRNA coding for neuroprotective proteins were measured bilaterally in parietal cortex using Northern blot analysis. Levels of c-fos mRNA and brain- derived neurotrophic factor (BDNF) mRNA were markedly elevated at 0 and 2 hours, but not 24 hours after CSD. Tissue plasminogen activator (tPA) mRNA levels were also significantly increased at 0 and 2 hours, but not 24 hours after CSD. Levels of the 72-kDa heat-shock protein (hsp72) mRNA were not significantly increased by CSD, except for a small elevation (20%) at 2 hours recovery. Levels of the 73-kDa heat-shock cognate (hsc73) mRNA were slightly, but significantly, increased at 2 and 24 hours of recovery. Finally, levels of mRNA for protease nexin-1 and glutamine synthetase were not significantly altered by CSD at any time studied. The current results support the hypothesis that neuronal tolerance to ischemia after CSD may be mediated by increased expression of FOS, BDNF, or tPA, but not by increased expression of hsp72, hsc73, nexin-1; or glutamine synthetase.

Original languageEnglish (US)
Pages (from-to)1308-1315
Number of pages8
JournalJournal of Cerebral Blood Flow and Metabolism
Volume18
Issue number12
DOIs
StatePublished - Dec 1998

Keywords

  • Cortical spreading depression
  • Immediate-early genes
  • Ischemic tolerance
  • Neuroprotection
  • Neurotrophic factors
  • Stress proteins

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology
  • Cardiology and Cardiovascular Medicine

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