NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Shear stress activation of platelets with subsequent refractoriness.

Author(s): Aursnes I, Sundal J, Nome T

Publication: Thromb Res, 1987, Vol. 45, Page 29-37

PubMed ID: 3563976 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of anticoagulant, time at room temperature, mixing speed, and centrifugation on platelet aggregation in whole blood.

Conclusion of Paper

Mixing whole blood with a magnetic stir bar induced platelet aggregation in a speed-dependent manner, but the response was also dependent on time at room temperature and which anticoagulant was used. Similarly, platelet aggregation was induced by centrifugation and could be attenuated by EDTA or increased by the addition of adenosine diphosphate (ADP).

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of anticoagulant, time at room temperature, mixing speed, and centrifugation on platelet aggregation. Blood was obtained with minimal stasis, and the first 2 mL were discarded. Specimens were mixed with a magnetic stir bar.

    Summary of Findings:

    Platelet aggregation occurred in response to stirring without ADP addition, but the response was dependent on time at room temperature prior to mixing, with the greatest response observed in specimens held at room temperature for 17 min and the least in specimens left at room temperature for 26 min. The authors report that platelet aggregation in response to specimen mixing did not occur if the specimen was anticoagulated with citrate instead of soybean trypsin inhibitor (SBTI) or if the specimen was heated to 37 degrees C prior to mixing. The subsequent addition of ADP to specimens, after mixing-induced aggregation, resulted in only a very small additional response. When ADP was added at the commencement of stirring, the aggregation response increased with increasing stirring speed, and while the trend was the same in citrated specimens, the magnitude of the changes was smaller. The platelet concentration generally decreased at a lower sampling level within the tubes after a 3 min centrifugation, but the effect was attenuated when platelet aggregation was inhibited by EDTA, and the sampling level effect was exaggerated when SBTI-anticoagulated specimens were stimulated by the addition of ADP. Beta-thromboglobulin was released when specimens were centrifuged for 10 min.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Not specified
    Platform:
    AnalyteTechnology Platform
    Cell count/volume Flow cytometry
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Aliquots and Components Biospecimen mixing 0 rpm
    600 rpm
    1200 rpm
    Storage Time at room temperature 8 min
    17 min
    26 min
    Biospecimen Acquisition Anticoagulant Citrate
    EDTA
    Soybean trypsin inhibitor
    Biospecimen Aliquots and Components Biospecimen components 20 mm below top of tube
    40 mm below to of tube
    60 mm below top of tube
    Biospecimen Aliquots and Components Blood and blood products Multiple sampling positions examined

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