Article detail · 2004
Reperfusion Induced Oxidative Nitrative Injury to Neurovascular Unit After Focal Cerebral Ischemia
- 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)
29 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
- Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
- Pericyte contraction induced by oxidative nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
- Pericyte contraction induced by oxidative nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
- Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
- Can restoring incomplete microcirculatory reperfusion improve stroke outcome after thrombolysis 2012
- Brain microvascular pericytes in health and disease 2011
- Cerebral microvascular pericytes and neurogliovascular signaling in health and disease 2015
- Microvascular protection is essential for successful neuroprotection in stroke 2012
- Pericytes in the brain and heart: functional roles and response to ischaemia and reperfusion 2024
- Pericytes in Ischemic Stroke 2019