The antidepressant 5-HT2A receptor antagonists pizotifen and cyproheptadine inhibit serotonin-enhanced platelet function

PLoS One. 2014 Jan 23;9(1):e87026. doi: 10.1371/journal.pone.0087026. eCollection 2014.

Abstract

There is considerable interest in defining new agents or targets for antithrombotic purposes. The 5-HT2A receptor is a G-protein coupled receptor (GPCR) expressed on many cell types, and a known therapeutic target for many disease states. This serotonin receptor is also known to regulate platelet function. Thus, in our FDA-approved drug repurposing efforts, we investigated the antiplatelet activity of cyproheptadine and pizotifen, two antidepressant 5-HT2A Receptor antagonists. Our results revealed that cyproheptadine and pizotifen reversed serotonin-enhanced ADP-induced platelet aggregation in vitro and ex vivo. And the inhibitory effects of these two agents were found to be similar to that of EMD 281014, a 5-HT2A Receptor antagonist under development. In separate experiments, our studies revealed that these 5-HT2A receptor antagonists have the capacity to reduce serotonin-enhanced ADP-induced elevation in intracellular calcium levels and tyrosine phosphorylation. Using flow cytometry, we also observed that cyproheptadine, pizotifen, and EMD 281014 inhibited serotonin-enhanced ADP-induced phosphatidylserine (PS) exposure, P-selectin expression, and glycoprotein IIb-IIIa activation. Furthermore, using a carotid artery thrombosis model, these agents prolonged the time for thrombotic occlusion in mice in vivo. Finally, the tail-bleeding time was investigated to assess the effect of cyproheptadine and pizotifen on hemostasis. Our findings indicated prolonged bleeding time in both cyproheptadine- and pizotifen-treated mice. Notably, the increases in occlusion and bleeding times associated with these two agents were comparable to that of EMD 281014, and to clopidogrel, a commonly used antiplatelet drug, again, in a fashion comparable to clopidogrel and EMD 281014. Collectively, our data indicate that the antidepressant 5-HT2A antagonists, cyproheptadine and pizotifen do exert antiplatelet and thromboprotective effects, but similar to clopidogrel and EMD 281014, their use may interfere with normal hemostasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Diphosphate / pharmacology
  • Animals
  • Antidepressive Agents / pharmacology*
  • Blotting, Western
  • Calcium / metabolism
  • Carotid Artery Thrombosis / drug therapy*
  • Carotid Artery Thrombosis / metabolism
  • Carotid Artery Thrombosis / pathology
  • Clopidogrel
  • Cyproheptadine / pharmacology*
  • Flow Cytometry
  • Hemorrhage / drug therapy
  • Hemorrhage / metabolism
  • Hemorrhage / pathology
  • Humans
  • Immunoprecipitation
  • Indoles / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Piperazines / pharmacology
  • Pizotyline / pharmacology*
  • Platelet Activation / drug effects
  • Platelet Aggregation / drug effects
  • Platelet Aggregation / physiology*
  • Platelet Aggregation Inhibitors / pharmacology*
  • Platelet Function Tests
  • Receptor, Serotonin, 5-HT2A / chemistry
  • Serotonin / pharmacology*
  • Serotonin Antagonists / pharmacology
  • Serotonin Receptor Agonists / pharmacology
  • Ticlopidine / analogs & derivatives
  • Ticlopidine / pharmacology

Substances

  • Antidepressive Agents
  • EMD 281014
  • Indoles
  • Piperazines
  • Platelet Aggregation Inhibitors
  • Receptor, Serotonin, 5-HT2A
  • Serotonin Antagonists
  • Serotonin Receptor Agonists
  • Pizotyline
  • Cyproheptadine
  • Serotonin
  • Adenosine Diphosphate
  • Clopidogrel
  • Ticlopidine
  • Calcium

Grants and funding

This research was supported by funds provided by the College of Pharmacy (to F.T.K). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.