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  • factor XIII  (1)
  • proteolytically cleaved receptor  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 129 (2000), S. 314-317 
    ISSN: 1573-8221
    Keywords: mast cells ; proteolytically cleaved receptor ; thrombin ; β-hexosaminidase ; heparin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In vivo experiments on the model of wound healing showed that thrombin and thrombin receptor agonist TRAP-6 stimulated heparin secretion by mast cells in rat subcutaneous fat: the saturation of mast cells with heparin decreased, while degranulation and granulolysis increased.In vitro studies showed that TRAP-6 caused a dose-dependent release of β-hexosaminidase from peritoneal mast cells. TRAP-6 also induced heparin release from these cells and inhibition of amidase activity of thrombin. Heparin released from mast cells had low anticoagulant activity. These data suggest that activation of mast cells with thrombin is mediated by PAR-1.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 80 (1975), S. 737-739 
    ISSN: 1573-8221
    Keywords: factor XIII ; platelets ; aggregation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract During platelet aggregation induced by ADP or thrombin, a reduction in the activity of factor XIII is observed in platelet-enriched rat plasma. On the addition of active factor XIII (XIIIa) to this plasma, besides the increased ADP-induced aggregation, activity of factor III in the plasma is reduced. In the case of thrombin-induced platelet aggregation, addition of factor XIIIa is accompanied by a marked decrease in its activity in the plasma. The degree of aggregation under these circumstances is lower than in control samples. The observed differences in the character of aggregation taking place in the presence of factor XIIIa, when different aggregants (ADP and thrombin) are used, are evidently due to interaction between active factor XIII and thrombin added to the plasma as the aggregant.
    Type of Medium: Electronic Resource
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