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Microvascular protection is essential for successful neuroprotection in stroke
Currently, the best way of neuroprotection for acute ischemic stroke appears to be restoration of blood flow to the ischemic area by thrombolysis. Unfortunately, a short therapeutic time window as well as thrombolysis‐induced bleeding and edema limit the use of recanalization therapies. Here, we rev...
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Published in: | Journal of neurochemistry 2012-11, Vol.123 (s2), p.2-11 |
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description | Currently, the best way of neuroprotection for acute ischemic stroke appears to be restoration of blood flow to the ischemic area by thrombolysis. Unfortunately, a short therapeutic time window as well as thrombolysis‐induced bleeding and edema limit the use of recanalization therapies. Here, we review the evidence suggesting that ischemia/reperfusion‐induced microvascular injury plays a critical role in determining tissue survival after recanalization in focal cerebral ischemia by disrupting the blood–brain barrier integrity and promoting microcirculatory clogging. Among many complex mechanisms of the ischemia–reperfusion injury, overproduction of oxygen and nitrogen radicals on the microvascular wall appears to significantly contribute to these pathological processes. These developments bring about the exciting possibility that effective suppression of oxidative/nitrative stress during pharmacological or interventional re‐opening of the occluded artery may significantly improve the outcome of recanalization therapies in stroke patients by improving microcirculatory reflow as well as by preventing hemorrhagic conversion and vasogenic edema. They also point to the critical (but partly neglected) importance of the microcirculation in neuroprotection. |
doi_str_mv | 10.1111/j.1471-4159.2012.07938.x |
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Unfortunately, a short therapeutic time window as well as thrombolysis‐induced bleeding and edema limit the use of recanalization therapies. Here, we review the evidence suggesting that ischemia/reperfusion‐induced microvascular injury plays a critical role in determining tissue survival after recanalization in focal cerebral ischemia by disrupting the blood–brain barrier integrity and promoting microcirculatory clogging. Among many complex mechanisms of the ischemia–reperfusion injury, overproduction of oxygen and nitrogen radicals on the microvascular wall appears to significantly contribute to these pathological processes. 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Neurochem</addtitle><description>Currently, the best way of neuroprotection for acute ischemic stroke appears to be restoration of blood flow to the ischemic area by thrombolysis. Unfortunately, a short therapeutic time window as well as thrombolysis‐induced bleeding and edema limit the use of recanalization therapies. Here, we review the evidence suggesting that ischemia/reperfusion‐induced microvascular injury plays a critical role in determining tissue survival after recanalization in focal cerebral ischemia by disrupting the blood–brain barrier integrity and promoting microcirculatory clogging. Among many complex mechanisms of the ischemia–reperfusion injury, overproduction of oxygen and nitrogen radicals on the microvascular wall appears to significantly contribute to these pathological processes. 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subjects | Animals Blood vessels Blood-Brain Barrier - drug effects Blood-Brain Barrier - physiology Brain cerebral ischemia Humans Microvessels - physiology Neurochemistry Neuroprotective Agents - therapeutic use neurovascular unit nitric oxide Nitrogen Oxides - metabolism no-reflow Oxidative stress Oxidative Stress - drug effects Oxidative Stress - physiology pericyte peroxynitrite Reperfusion Injury - drug therapy Reperfusion Injury - prevention & control Stroke Stroke - pathology Stroke - physiopathology Stroke - therapy |
title | Microvascular protection is essential for successful neuroprotection in stroke |
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