Related Experiment Videos
Whole blood platelet aggregation in humans and animals: a comparative study
M V Soloviev1, Y Okazaki, H Harasaki
1Research Institute, The Cleveland Clinic Foundation, Cleveland, Ohio, 44195, USA.
The Journal of Surgical Research
|March 26, 1999
Summary
Human, dog, and calf platelets show distinct responses to agonists. Collagen and ADP are best for studying platelet aggregation across species, while thrombin is recommended for adenosine triphosphate (ATP) release.
Area of Science:
- Biomedical Engineering
- Hematology
- Comparative Physiology
Background:
- Interspecies differences in platelet activity are crucial for cardiovascular device evaluation.
- Limited characterization of platelet response to agonists across species.
Purpose of the Study:
- To measure and compare platelet aggregation and adenosine triphosphate (ATP) release in response to various agonists in human, dog, and calf blood.
- To identify optimal agonists for interspecies platelet function studies.
Main Methods:
- Whole blood impedance lumi-aggregometry used to analyze platelet aggregation and ATP release.
- Blood samples from humans (n=19), dogs (n=19), and calves (n=7) were tested.
- Six agonists were used: collagen, ristocetin, arachidonic acid, thrombin, adenosine diphosphate (ADP), and epinephrine at varying concentrations.
Main Results:
- Collagen (1 microg/ml) and ADP (5, 10, 20 microM) induced aggregation and ATP release in all species.
- Canine platelets responded to all agonists; human platelets responded to all except epinephrine at specific doses.
- Bovine platelets showed limited response (collagen, ADP, thrombin), with significantly lower aggregation and ATP release compared to humans and dogs.
Conclusions:
- Significant interspecies variations exist in platelet reactivity to agonists.
- Collagen (1 microg/ml) and ADP (10 microM) are recommended for consistent whole blood platelet aggregation studies.
- Thrombin (1 U/ml) is the recommended agonist for adenosine triphosphate (ATP) release assays across species.