Identification, characterization, and inhibition of the platelet ADP receptors.

Abstract

Adenosine diphosphate (ADP) plays a crucial role in hemostasis and thrombosis, and its receptors are potential targets for antithrombotic drugs. Two G-protein-coupled P2 receptors contribute to platelet aggregation: the P2Y1 receptor initiates aggregation through mobilization of calcium stores, whereas the P2Y12 receptor coupled to adenylyl cyclase inhibition is essential for a full aggregation response to ADP and the stabilization of aggregates. The latter is defective in certain patients with a selective congenital deficiency of aggregation to ADP. It is also the target of the antithrombotic drug clopidogrel and of adenosine triphosphate analogues and other compounds currently under evaluation. In addition, the P2X1 ionotropic receptor is present in platelets, but its role is not yet completely known. Studies in P2Y1-knockout mice and experimental thrombosis models using selective P2Y1 antagonists have shown that the P2Y1 receptor, like the P2Y12 receptor, is a potential target for new antithrombotic drugs.

• Authors: C Gachet
• Journal: International journal of hematology (Int J Hematol) Vol. 74 Issue 4 Pg. 375-81 (Dec 2001) ISSN: 0925-5710 [Print] Japan
• PMID: 11794691 (Publication Type: Journal Article, Review)

Chemical References

• Fibrinolytic Agents
• Purinergic P2 Receptor Antagonists
• Receptors, Purinergic P2

Topics

• Animals
• Blood Platelets (chemistry, physiology)
• Fibrinolytic Agents (chemistry, pharmacology, therapeutic use)
• Humans
• Platelet Aggregation (drug effects)
• Purinergic P2 Receptor Antagonists
• Receptors, Purinergic P2 (genetics, physiology)