Thromb Haemost 1983; 49(03): 173-175
DOI: 10.1055/s-0038-1657355
Original Article
Schattauer GmbH Stuttgart

The Effect of Serotonin Inhibition on Initial Microvessel Hemostasis and Platelet Aggregation In Vivo

Authors

  • D Bergqvist

    The Departments of Surgery and Experimental Research, Malmö General Hospital, Malmö and Department of Experimental Medicine, Pharmacia AB, Uppsala, Sweden
  • S Arvidsson

    The Departments of Surgery and Experimental Research, Malmö General Hospital, Malmö and Department of Experimental Medicine, Pharmacia AB, Uppsala, Sweden
  • C O Esquivel

    The Departments of Surgery and Experimental Research, Malmö General Hospital, Malmö and Department of Experimental Medicine, Pharmacia AB, Uppsala, Sweden
  • B Lindblad

    The Departments of Surgery and Experimental Research, Malmö General Hospital, Malmö and Department of Experimental Medicine, Pharmacia AB, Uppsala, Sweden
  • U Haglund

    The Departments of Surgery and Experimental Research, Malmö General Hospital, Malmö and Department of Experimental Medicine, Pharmacia AB, Uppsala, Sweden
Further Information

Publication History

Received 14 January 1983

Accepted 17 March 1983

Publication Date:
18 July 2018 (online)

Preview

Summary

The role of serotonin (5-HT) in initial microvascular hemostasis is not fully understood. This study was made to evaluate the effect on hemostatic plug formation and laser-induced arteriolar microembolism of different substances which counteract the effect of 5-HT. Hemostatic plug formation time and stability was measured in the rabbit mesenteric microcirculation and laserinduced embolism in the rabbit ear chamber. Ketanserine, a selective 5-HT2-receptor blocker shortened arteriolar hemostatic plug formation time. Dihydroergotamine, an unselective blocker (with 5-HT- and α-adrenergic receptor affinity) increased venular hemostatic plug formation time and also decreased the hemostatic plug stability. Laser-induced platelet embolism was unaltered after both ketanserine and dihydroergotamine administration. The magnitude of these changes seems to exclude an important effect of 5-HT in initial microvessel hemostasis or on platelet activity.