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Published on: March 22, 2024
Levosimendan has an inhibitory effect on platelet function
Kürşat Kaptan1, Kürşad Erinç, Ahmet Ifran
1Department of Hematology, Gülhane Military Medical Academy, Ankara, Turkey. mkkaptan@hotmail.com
Insights
Levosimendan significantly inhibits platelet aggregation induced by ADP and collagen in vitro. This effect was concentration-dependent, suggesting a potential influence on platelet function during therapeutic use.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Levosimendan is a cardiac inotrope enhancing contractility and causing vasodilation.
- Its effects on platelet function remain largely uncharacterized despite clinical use in heart failure.
Purpose of the Study:
- To investigate the in vitro effect of levosimendan on platelet aggregation.
- To determine if clinically relevant concentrations of levosimendan influence platelet response to agonists.
Main Methods:
- Whole blood from 12 healthy volunteers was incubated with three concentrations of levosimendan (10, 25, 45 ng/ml).
- Platelet aggregation was measured using adenosine diphosphate (ADP) and collagen as agonists.
- Inhibition of platelet aggregation was assessed in platelet-rich plasma after incubation.
Main Results:
- Levosimendan significantly inhibited platelet aggregation induced by both ADP and collagen across all tested concentrations.
- A dose-dependent relationship was observed between levosimendan concentration and the degree of platelet aggregation inhibition.
- The drug also significantly inhibited the secondary aggregation wave induced by ADP.
Conclusions:
- Levosimendan demonstrates a significant inhibitory effect on human platelet aggregation in vitro.
- These findings suggest that levosimendan may modulate platelet function at clinically relevant concentrations.
- Further studies are warranted to explore the clinical implications of levosimendan's antiplatelet effects.
Abstract:
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 microg/kg/min. Each concentration of levosimendan solution and a control diluent without levosimendan were incubated with whole blood at 37 degrees C. After incubation for 15 min, aggregation responses were evaluated with adenosine diphosphate (ADP) (5 and 10 microM) and collagen (2 and 5 microg/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.
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