Key result
ADP and bovine collagen trigger irreversible equine platelet aggregation while epinephrine yields no response.
Why the study?
Equine platelet aggregation responses to various agonists and conditions were not fully characterized to establish a reliable in vitro assessment method.
The study establishes a reliable in vitro method to assess equine platelet aggregation and characterizes the specific responses to various common agonists.
Answers are grounded in this paper and cite their sources.
Equine platelet agonist responses characterized in vitro; leaves open translation to clinical antithrombotic strategies in horses.
Equine platelet aggregation responses to bovine collagen, adenosine diphosphate (ADP), serotonin, epinephrine, and arachidonate in a platelet aggregometer were recorded. Equine platelets exhibited irreversible aggregation when incubated with ADP at a final concentration of 10 microM and bovine collagen. A secondary aggregation wave was recorded from platelets from certain horses at final ADP concentrations of 1 to 5 microM. Serotonin and arachidonate induced a weak reversible aggregation response, but a response was not observed following epinephrine addition. Equine platelet aggregation was influenced by concentration of anticoagulant (sodium citrate). Platelet aggregation responses at 37 C were indistinguishable from those recorded at 39 C. Platelet aggregation responses also were altered if the aggregation tests were not performed within 4 hours of blood sample acquisition. An assessment of platelet aggregation from multiple blood samples from the same horse indicated that the procedures described provide a reliable method to assess equine platelet aggregation in vitro.
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Meyers et al. (1979) studied Equine platelet aggregation. Platelet aggregants (bovine collagen, ADP, serotonin, epinephrine, arachidonate) was evaluated on Platelet aggregation response. Equine platelets exhibited irreversible aggregation with 10 microM ADP and bovine collagen, weak reversible aggregation with serotonin and arachidonate, and no response to epinephrine.
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