Inhibition of integrin αvβ3 reduces blood-brain barrier breakdown in focal ischemia in rats

Norihito Shimamura, Gerald Matchett, Ihsan Solaroglu, Tamiji Tsubokawa, Hiroki Ohkuma, John Zhang

Research output: Contribution to journalArticle

34 Scopus citations

Abstract

Ischemic stroke is a major cause of morbidity and mortality in industrialized nations. We tested the effect of postischemic treatment of cyclo-RGDfV (cRGDfV), a selective inhibitor of integrin αvβ3, in the middle cerebral artery occlusion (MCAO) model of ischemic stroke in rats. Rats were randomly divided into three groups: sham operation (n = 13), MCAO with no treatment (n = 18), and MCAO with cRGDfV treatment (n = 28). Focal ischemia was induced with the suture occlusion method for 2 hr, and treatment was given 1 hr after reperfusion (3 hr after ischemia). All animals were sacrificed 24 hr after reperfusion. Assessment included neurological scores, infarction volumes, brain water content, Evans blue exudation, IgG exudation, histology, immunohistochemistry, and Western blotting. Treatment with cRGDfV ameliorated neurological deficits, reduced brain edema, and reduced exudation of Evans blue dye and IgG, but failed to reduce infarction volumes. Western blotting showed a reduction in phosphorylation of one subset of vascular endothelial growth factor (VEGF) receptors in the cRGDfV treatment group. Western blotting also demonstrated a significant reduction of fibrinogen in the cRGDfV treatment group. We conclude that poststroke treatment with cRGDfV reduces blood-brain barrier breakdown in focal ischemia, possibly through inhibition of VEGF-mediated vascular breakdown.

Original languageEnglish (US)
Pages (from-to)1837-1847
Number of pages11
JournalJournal of Neuroscience Research
Volume84
Issue number8
DOIs
StatePublished - Dec 2006

Keywords

  • Flk-1
  • Integrin αvβ3
  • MCAO
  • VEGF
  • cRGDfV

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience

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