Platelet P2 receptors: old and new targets for antithrombotic drugs

Abstract

Platelets possess three P2 receptors for adenine nucleotides: P2Y₁ and P2Y₁₂, which interact with ADP, and P2X₁, which interacts with ATP. The interaction of adenine nucleotides with their platelet receptors plays an important role in thrombogenesis. The thienopyridine ticlopidine, an antagonist of the platelet P2Y₁₂ ADP receptor, reduces the incidence of vascular events in patients at risk, but it also has some important drawbacks: a relatively high incidence of toxic effects; delayed onset of action; high inter-individual variability in response. Another thienopyridine, clopidogrel, has superseded ticlopidine, because it is an efficacious antithrombotic drug and is less toxic than ticlopidine. However, the high inter-patient variability in response still remains an important issue. These drawbacks justify the continuing search for agents that can further improve the clinical outcome of patients with atherosclerosis through greater efficacy and/or safety. A new thienopyridyl compound prasugrel, which is characterized by higher potency and faster onset of action compared with clopidogrel, is currently under clinical evaluation. Two direct and reversible P2Y₁₂ antagonists, cangrelor and AZD6140, have very rapid onset and reversal of platelet inhibition, which make them attractive alternatives to thienopyridines, especially when rapid inhibition of platelet aggregation or its quick reversal are required. Along with new P2Y₁₂antagonists, inhibitors of the other platelet receptor for ADP, P2Y₁, and of the receptor for ATP, P2X₁, are under development and may prove to be effective antithrombotic agents.

Keywords::

• ADP
• antiplatelet agents
• ATP
• clopidogrel
• P2 receptors
• platelets
• prasugrel
• thienopyridines
• thrombosis
• ticlopidine