(Stroke. 2004;35:354.)
© 2004 American Heart Association, Inc.
Advances in Stroke 2003 |
From the Neuroprotection Research Laboratory (E.H.L.), Departments of Radiology and Neurology, Massachusetts General Hospital, and Program in Neuroscience, Harvard Medical School, Charlestown, Mass; Department of Neurology (J.P.B.), University of Cincinnati, Cincinnati, Ohio; and Neurovascular Regulation and Stroke Laboratory (M.A.M.), Departments of Radiology and Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Charlestown, Mass.
Correspondence to Eng H. Lo, Neuroprotection Research Laboratory, Harvard Medical School, MGH East 149-2401, Charlestown, MA 02129. E-mail Lo@helix.mgh.harvard.edu
Key Words: Advances in Stroke blood-brain barrier matrix metalloproteinase proteolysis reperfusion injury tissue plasminogen activator
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
One of the major recommendations emerging from the NINDS Stroke Progress Review Group was to shift the emphasis from a purely neurocentric view of cell death toward a more integrative approach whereby responses in all brain cells and matrix are considered during cerebral ischemia (see Figure). The concept of the neurovascular unit (fundamentally comprising endothelium, astrocyte, and neuron) provides a modular framework where cell-cell signaling and cell-matrix interactions mediate the overall tissue response to stroke and its treatments.1 There is no doubt that reperfusing blood vessels mechanically or pharmacologically prevents cell death and rescues brain when performed in a timely manner, as it does in ischemic myocardium. However, under some circumstances, thrombolysis and reperfusion lead to cerebral hemorrhage and edema. Here, we examine the hypothesis that beneficial versus potentially deleterious outcomes after tissue plasminogen activator (tPA) stroke therapy may relate in part to matrix proteolysis within the neurovascular unit, and review recent advances in this area.
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tPA: More Than Clot Lysis
More than 7 years after the major ECASS and NINDS trials,2,3 use of tPA therapy remains limited.4 In part, this may be due to narrow time-to-treatment windows and apparent complications of hemorrhage and brain injury.5 The primary action of
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