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Levosimendan has an inhibitory effect on platelet function
Author(s) -
Kaptan Kürşat,
Erinç Kürşad,
Ifran Ahmet,
Yıldırım Vedat,
Uzun Mehmet,
Beyan Cengiz,
Işık Ersoy
Publication year - 2008
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.20999
Subject(s) - levosimendan , platelet , contractility , whole blood , pharmacology , medicine , adenosine diphosphate , chemistry , heart failure , platelet aggregation
Levosimendan enhances cardiac contractility by increasing myocyte sensitivity to calcium, and induces vasodilatation. Although studies have evaluated the efficacy of levosimendan in heart failure, it is not clear whether it might produce functional influence on platelet response. In this study, the effect of levosimendan on platelet aggregation was investigated. Platelet function tests were performed in 12 healthy male volunteers. Three concentrations of levosimendan solution were prepared that would result in 10, 25, and 45 ng/ml levosimendan concentrations in the blood similar to that observed after clinical therapeutic intravenous application of 0.05–0.1 μg/kg/min. Each concentration of levosimendan solution and a control diluent without levosimendan were incubated with whole blood at 37°C. After incubation for 15 min, aggregation responses were evaluated with adenosine diphosphate (ADP) (5 and 10 μM) and collagen (2 and 5 μg/ml) in platelet‐rich plasma. Preincubation with all dilutions of levosimendan inhibited aggregation of platelets induced by ADP and collagen significantly. Levosimendan also inhibited significantly the secondary wave of platelet aggregation induced by ADP. The results showed that there was a relationship between levosimendan concentration and inhibition of platelet aggregation. In conclusion, this study with an in vitro model showed that levosimendan had a significant inhibitory effect on platelets in clinically relevant doses. Am. J. Hematol., 2008. © 2007 Wiley‐Liss, Inc.