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Platelet Adhesion and Aggregation Under Flow using Microfluidic Flow Cells
Published on: October 27, 2009
Inhibitory effect of Ginkgo biloba extract on human platelet aggregation
A K Dutta-Roy1, M J Gordon, C Kelly
1Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, Scotland, UK. adr@rri.sari.ac.uk
Platelets
|June 28, 2006
Summary
Ginkgo biloba extract (GBE) effectively inhibits human platelet aggregation in whole blood and plasma. This extract may serve as a potential oral anti-platelet therapeutic agent.
Area of Science:
- Pharmacology
- Biochemistry
- Cardiovascular Research
Background:
- Platelet aggregation plays a crucial role in thrombosis.
- Flavonoids and Ginkgo biloba extract (GBE) are investigated for their potential anti-platelet effects.
Purpose of the Study:
- To investigate the effects of pure flavonoids and GBE on human platelet aggregation.
- To elucidate the mechanisms underlying GBE's anti-platelet activity.
Main Methods:
- Platelet aggregation assays were performed using platelet-rich plasma (PRP), gel-filtered platelets (GFP), and whole blood.
- Effects on thromboxane A2 (TxA2) production, platelet membrane fluidity, and cyclic AMP (cAMP) levels were measured.
Main Results:
- GBE significantly inhibited ADP- and collagen-induced platelet aggregation in a dose-dependent manner across PRP, GFP, and whole blood.
- While GBE and some flavonoids reduced TxA2 production, no direct correlation with aggregation inhibition was found.
- GBE increased platelet cAMP levels, suggesting a mechanism involving reduced intracellular calcium (Ca2+).
Conclusions:
- GBE demonstrates potent anti-platelet activity, particularly in whole blood, at low concentrations.
- The anti-platelet effects of GBE are likely mediated through mechanisms involving cAMP and potentially Ca2+ regulation.
- GBE shows promise as an orally administered therapeutic agent for preventing platelet aggregation.
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