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Article detail · 2004

Reperfusion Induced Oxidative Nitrative Injury to Neurovascular Unit After Focal Cerebral Ischemia

Journal

Stroke

ISSN 0039-2499

YÖKSİS OpenAlex Open access · green SJR Q1 JCR Q1 Citations 275 Top 10% Percentile 96.6% FWCI 5.66
Year
2004
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • YÖKSİS venue Stroke
  • Catalog match (ISSN) Stroke
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

OpenAlex · English

BACKGROUND AND PURPOSE: Use of thrombolysis in stroke is limited by a short therapeutic window because delayed reperfusion may cause brain hemorrhage and edema. Available evidence suggests a role for superoxide, NO, and peroxynitrite in reperfusion-induced injury. However, depending on their cellular origin and interactions between them, these molecules may exert protective or deleterious actions, neither of which is characterized in the intact brain. METHODS: Using fluorescent probes, we determined superoxide and peroxynitrite formation within neurons, astrocytes, and endothelium, and the association between oxidative/nitrative stress and vascular injury in mice brains subjected to 2-hour middle cerebral artery occlusion and 3 or 5 hours of reperfusion. RESULTS: Both signals were colocalized, suggesting that the main source of peroxynitrite in the reperfused brain was a reaction between superoxide and NO. Superoxide and peroxynitrite formation was particularly intense in microvessels and astrocytic end-feet surrounding them, and overlapped with dense mitochondrial labeling. Sites of oxidative/nitrative stress on microvessels were colocalized with markers of vascular injury such as Evans blue (EB) leakage and matrix metalloproteinase-9 (MMP-9) expression, suggesting an association between peroxynitrite and microvascular injury. Supporting this idea, partial inhibition of endothelial NO synthesis at reperfusion with a low dose of L-nitroarginine (1 mg/kg IP) reduced 3-nitrotyrosine formation in microvessels and EB extravasation. CONCLUSIONS: During reperfusion, intense superoxide, NO, and peroxynitrite formation on microvessels and surrounding end-feet may lead to cerebral hemorrhage and edema by disrupting microvascular integrity. Combination of thrombolysis with agents diminishing oxidative/nitrative stress may reduce reperfusion-induced injury and extend the therapeutic window for thrombolysis.

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

275 citations

OpenAlex cited_by_count (cache / database)

Authors

  1. Yasemin GursoyOzdemir
  2. ALP CAN ANKARA ÜNİVERSİTESİ
  3. TURGAY DALKARA İHSAN DOĞRAMACI BİLKENT ÜNİVERSİTESİ