P2 receptors, platelet function and pharmacological implications

Christian Gachet

doi:10.1160/TH07-11-0673

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2008; 99(03): 466-472
DOI: 10.1160/TH07-11-0673

Theme Issue Article

Schattauer GmbH

P2 receptors, platelet function and pharmacological implications

Christian Gachet

¹Institut National de la Santé et de la Recherche Médicale, U311, Strasbourg, France; Etablissement Français du Sang-Alsace, Strasbourg, France; Université Louis Pasteur, Strasbourg, France

› Author Affiliations

Abstract

Summary

ADP and ATP play a crucial role in platelet activation and their receptors are potential targets for antithrombotic drugs. The ATP-gated cation channel P2X₁ and the two G protein-coupled ADP receptors, P2Y₁ and P2Y₁₂, selectively contribute to platelet aggregation and formation of a thrombus.Owing to its central role in the growth and stabilization of a thrombus, the P2Y₁₂ receptor is an established target of antithrombotic drugs like the thienopyridines clopidogrel or prasugrel, or competitive antag-onists such as cangrelor or AZD6140.The optimal inhibition of this receptor to reach clinical efficacy while preserving patients from unacceptable bleeding is a matter of debate. On the other hand, studies in P2Y₁ and P2X₁ knockout mice and using selective P2Y₁ and P2X₁ antagonists have shown that these receptors are also attractive targets for new antithrombotic compounds. Finally, the regulation by the P2 receptors of the platelet involvement in inflammatory processes is also briefly discussed.

Keywords

Haemostasis - thrombosis - ADP - P2Y₁ - P2Y₁₂ - P2X₁ - antiplatelet drugs - thienopyridine - clopidogrel - prasugrel - AZD6140 - cangrelor

Full Text

References

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