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Basic fibroblast growth factor increases collateral blood flow in spontaneously hypertensive rats
Sunita Srivastava1, Ronald L Terjung, H T Yang
1Section of Vascular Surgery, University of Michigan, Ann Arbor, MI 48109, USA.
Summary
Basic fibroblast growth factor (bFGF) effectively enhanced collateral circulation and blood flow in hypertensive rats. High-dose bFGF also reduced blood pressure, suggesting restored nitric oxide bioavailability for arteriogenesis.
Area of Science:
- Cardiovascular Science
- Regenerative Medicine
- Hypertension Research
Background:
- Spontaneously hypertensive rats (SHR) exhibit reduced ischemia-induced angiogenic responses.
- Collateral circulation is crucial for blood flow restoration after arterial occlusion.
Purpose of the Study:
- To evaluate the efficacy of exogenous basic fibroblast growth factor (bFGF) in promoting collateral circulation in hypertensive rats.
- To investigate the impact of bFGF on blood flow and blood pressure in SHR models.
Main Methods:
- Male SHR underwent femoral artery occlusion for 4 hours or 16 days, with intra-arterial infusion of vehicle or varying doses of bFGF (0.5, 5.0, 50.0 microg.kg-1.day-1).
- Maximal collateral-dependent hindlimb blood flow was measured using labeled microspheres during exercise.
- Blood pressure and heart rate were monitored pre-exercise.
Main Results:
- Femoral artery occlusion significantly reduced calf muscle blood flow by 95%.
- bFGF treatment dose-dependently increased blood flow, with significant improvements observed at all tested doses.
- High-dose bFGF (50.0 microg.kg-1.day-1) significantly reduced blood pressure by approximately 12%.
Conclusions:
- Exogenous bFGF effectively promotes collateral vessel remodeling and increases blood flow in hypertensive rats.
- bFGF may restore nitric oxide bioavailability, a key factor in arteriogenesis, potentially improving endothelial function in SHR.
- These findings suggest bFGF as a potential therapeutic agent for enhancing collateral circulation in hypertensive individuals.