ADP can induce aggregation of human platelets via both P2Y1 and P2T receptors

• Published in: British journal of pharmacology Vol. 129; no. 2; pp. 275 - 282
• Main Authors: Jarvis, G E, Humphries, R G, Robertson, M J, Leff, P
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-01-2000; Nature Publishing
• Subjects: adenosine‐3′‐phosphate‐5′‐phosphate; ADP; anti‐thrombotic agents; AR‐C67085; Biological and medical sciences; Blood. Blood coagulation. Reticuloendothelial system; heparinized platelet rich plasma; Medical sciences; P2T receptors; P2Y1 receptors; Pharmacology. Drug treatments; platelet aggregation; Aggregation; Human; Platelet; P2 Purinergic receptor; Mechanism of action; ADP; In vitro; Blood plasma
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1038/sj.bjp.0703046

In the present study we have investigated the roles of P2Y1 and P2T receptor subtypes in adenosine 5′‐diphosphate (ADP)‐induced aggregation of human platelets in heparinized platelet rich plasma.
The response to ADP can be characterized as the initial rate or the maximum or final extent of aggregation. The response profile is determined by the concentration of ADP used, being transient at lower and sustained at higher concentrations.
The P2Y1 receptor antagonist, adenosine‐3′‐phosphate‐5′‐phosphate (A3P5P) competitively antagonized the initial rate of aggregation (pKB 5.47) and transformed the response profile to a slowly developing but sustained response. Both maximum and final extents were also inhibited by A3P5P although not in a competitive manner (Schild slope <1).
The P2T receptor antagonist, AR‐C67085, competitively antagonized the final extent of aggregation (pKB 8.54), transforming the response profile to one of rapid, transient aggregation. Its effect on maximum extent (the most widely used index of aggregation) was complex, and further supported the involvement of both receptor subtypes in the aggregation response.
ADP‐induced aggregation is a complex phenomenon, the nature of which is determined by the relative occupancy of the two receptor subtypes. While P2Y1 receptor activation causes a rapid and transient aggregation, the extent of sustained aggregation is determined by the level of P2T receptor occupancy. Hence, detailed analysis of the aggregation response is essential to correctly define the purinergic pharmacology of the platelet and interpretation of results is critically dependent on the response index chosen.
British Journal of Pharmacology (2000) 129, 275–282; doi:10.1038/sj.bjp.0703046