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2-Vessel Occlusion/Hypotension: A Rat Model of Global Brain Ischemia
Published on: June 22, 2013
Reperfusion of ischemia in the heart or brain
Victor Gurewich1, David Segarnick2
1Department of Medicine, Harvard Medical School, Cambridge, Massachusetts.
Insights
Acute myocardial infarction (AMI) treatment using percutaneous coronary intervention (PCI) has delays impacting mortality. A sequential combination of tissue-type plasminogen activator and prourokinase offers a more effective reperfusion therapy for AMI and stroke.
Area of Science:
- Cardiovascular Medicine
- Thrombosis and Fibrinolysis
Background:
- Percutaneous coronary intervention (PCI) is the standard treatment for acute myocardial infarction (AMI).
- PCI procedures are lengthy (2-3 hours) and unsuitable for small artery clots.
- Inpatient catheterization for PCI causes reperfusion delays, directly correlating with increased AMI mortality.
Purpose of the Study:
- To evaluate an alternative treatment for AMI that overcomes PCI limitations.
- To explore a fibrinolytic therapy that mimics the body's natural clot-busting process.
Main Methods:
- The study focuses on a sequential combination therapy using tissue-type plasminogen activator and prourokinase.
- This approach aims to directly address the fibrinolytic process involved in AMI and ischemic stroke.
Main Results:
- The sequential fibrinolytic combination demonstrates effectiveness in treating AMI and ischemic stroke.
- This treatment strategy potentially reduces reperfusion delays compared to PCI.
Conclusions:
- A sequential combination of tissue-type plasminogen activator and prourokinase presents a more effective treatment for AMI and ischemic stroke.
- This fibrinolytic approach offers a promising alternative to PCI, particularly for specific clot types and reducing reperfusion times.
Abstract:
The current treatment of choice for an acute myocardial infarction (AMI) is an interventional procedure like percutaneous coronary intervention (PCI), which takes 2 to 3 hours and is not appropriate for clots in arteries smaller than the catheter. Because PCI requires inpatient catheterization, there is an inevitable delay in reperfusion of the ischemia. This delay was shown to have a linear relationship with AMI mortality. The longer the delay, from <5 minutes to >3 hours, the greater the cardiovascular disease mortality. Instead of PCI, a sequential combination of tissue-type plasminogen activator and prourokinase is the most effective treatment for conditions like AMI and ischemic stroke that mirrors the endogenous fibrinolytic process.
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