Tissue plasminogen activator (tPA) increase neuronal damage after focal cerebral ischemia in wild-type and tPA-deficient mice

YF Wang, SE Tsirka, S Strickland, PE Stieg… - Nature medicine, 1998 - nature.com
YF Wang, SE Tsirka, S Strickland, PE Stieg, SG Soriano, SA Lipton
Nature medicine, 1998nature.com
Intravenous tissue plasminogen activator (tPA) is used to treat acute stroke because of its
thrombolytic activity and its ability to restore circulation to the brain1, 2. However, this
protease also promotes neurodegeneration after intracerebral injection of excitotoxins such
as glutamate, and neuronal damage after a cerebral infarct is thought to be mediated by
excitotoxins3–8. To investigate the effects of tPA on cerebral viability during
ischemia/reperfusion, we occluded the middle cerebral artery in wild-type and tPA-deficient …
Abstract
Intravenous tissue plasminogen activator (tPA) is used to treat acute stroke because of its thrombolytic activity and its ability to restore circulation to the brain1,2. However, this protease also promotes neurodegeneration after intracerebral injection of excitotoxins such as glutamate, and neuronal damage after a cerebral infarct is thought to be mediated by excitotoxins3–8. To investigate the effects of tPA on cerebral viability during ischemia/reperfusion, we occluded the middle cerebral artery in wild-type and tPA-deficient mice with an intravascular filament. This procedure allowed us to examine the role of tPA in ischemia, independent of its effect as a thrombolytic agent. tPA-deficient mice exhibited ∼50% smaller cerebral infarcts than wild-type mice. Intravenous injection of tPA into tPA−/− or wild-type mice produced larger infarcts, indicating that tPA can increase stroke-induced injury. Since tPA promotes desirable (thrombolytic) as well as undesirable (neurotoxic) outcomes during stroke, future therapies should be aimed at countering the excitotoxic damage of tPA to afford even better neuropro-tection after an acute cerebral infarct.
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