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Impaired endogenous fibrinolytic capacity in prehypertensive men
K J Diehl1, B R Weil1, J J Greiner1
1Department of Integrative Physiology, Integrative Vascular Biology Laboratory, University of Colorado, Boulder, CO, USA.
Insights
Prehypertension is linked to reduced tissue-type plasminogen activator (t-PA) release from blood vessel linings. This impaired fibrinolytic function may explain the higher risk of atherothrombotic events in individuals with elevated blood pressure.
Area of Science:
- Cardiovascular Medicine
- Vascular Biology
- Hemostasis and Thrombosis
Background:
- Prehypertension (BP 120-139/80-89 mm Hg) is associated with increased atherothrombotic risk.
- The underlying mechanisms for this risk are not fully understood, but impaired endothelial fibrinolytic capacity is a possibility.
Purpose of the Study:
- To investigate whether vascular endothelial release of tissue-type plasminogen activator (t-PA) is impaired in men with prehypertension.
- To compare t-PA release in normotensive, prehypertensive, and hypertensive men.
Main Methods:
- In vivo assessment of net endothelial release of t-PA antigen.
- Intrabrachial infusions of bradykinin and sodium nitroprusside in 42 men (16 normotensive, 16 prehypertensive, 10 hypertensive).
- Measurement of t-PA release in response to vasoactive agents.
Main Results:
- Net endothelial t-PA release was approximately 25% lower in prehypertensive men compared to normotensive men (P<0.05).
- No significant difference in t-PA release was observed between hypertensive and prehypertensive groups.
- Sodium nitroprusside did not significantly affect t-PA release in any group.
Conclusions:
- Endothelial t-PA release is diminished in prehypertensive men.
- The impairment in t-PA release observed in clinical hypertension is already present in the prehypertensive state.
- Impaired endothelial fibrinolytic function may contribute to the increased atherothrombotic risk associated with prehypertension.
Abstract:
Prehypertension (blood pressure (BP) 120-139/80-89 mm Hg) is associated with an increased risk for future atherothrombotic events. Although the mechanisms underlying this elevated risk are not completely understood, one possibility is that prehypertension is associated with impaired endothelial fibrinolytic capacity. We tested the hypothesis that vascular endothelial release of tissue-type plasminogen activator (t-PA) is impaired in prehypertensive men. Net endothelial release of t-PA was determined, in vivo, in response to intrabrachial infusions of bradykinin (12.5, 25, 50 ng per 100 ml tissue per min) and sodium nitroprusside at (1.0, 2.0, 4.0 μg per 100 ml tissue per min) in 42 middle-age and older men: 16 normotensive (BP range: 100-119/57-79 mm Hg); 16 prehypertensive (BP range: 120-139/76-89 mm Hg); and 10 hypertensive (BP range: 140-150/74-100 mm Hg). Net release of t-PA antigen was ~25% lower (P<0.05) in the prehypertensive (-0.9 ± 0.8 to 42.4 ± 5.3 ng per 100 ml tissue per min) compared with the normotensive (0.5 ± 1.0 to 53.9 ± 6.5 ng per 100 ml tissue per min) men. There was no significant difference in t-PA release between the hypertensive (-1.8 ± 1.6 to 40.8 ± 6.6 ng per 100 ml tissue per min) and prehypertensive groups. Sodium nitroprusside did not significantly alter the t-PA release in any group. These data indicate that endothelial t-PA release is diminished in prehypertensive men. Further, the level of impairment in t-PA release seen with clinical hypertension is already apparent in the prehypertensive state. Impaired endothelial fibrinolytic function may underlie the increased atherothrombotic risk associated with BP in the prehypertensive range.
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