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Effects of the P 2 ‐purinoceptor antagonist, suramin, on human platelet aggregation induced by adenosine 5′‐diphosphate
Author(s) -
Hourani S.M.O.,
Hall D.A.,
Nieman C.J.
Publication year - 1992
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1992.tb14274.x
Subject(s) - suramin , schild regression , adenosine , adenosine diphosphate , chemistry , purinergic receptor , antagonist , medicine , endocrinology , platelet , agonist , competitive antagonist , receptor , pharmacology , biochemistry , biology , platelet aggregation
1 The effects of suramin, a trypanocidal drug which has been reported to be a P 2 ‐purinoceptor antagonist on smooth muscle, were investigated in human platelets, where adenosine 5′‐diphosphate (ADP) induces aggregation by acting on a subtype of purinoceptors which has been called P 2T . 2 Suramin (100 μ m ) had no inhibitory effect on ADP‐induced platelet aggregation in plasma, even after 40 min incubation in the presence of bacitracin, a peptidase inhibitor, and did not affect the ability of adenosine 5′‐triphosphate (ATP) (40 μ m ) to inhibit competitively ADP‐induced aggregation. This lack of effect of suramin on platelets in plasma is probably due to its extensive binding to plasma proteins. 3 In washed platelets, suramin (50–400 μ m ) acted as an apparently competitive antagonist, causing parallel shifts to the right of the log concentration‐response curve to ADP. No depression of the maximal response to ADP was observed at concentrations of suramin (50–150 μ m ) for which full log concentration‐response curves to ADP could be obtained, but the slope of the Schild plot was around 2, indicating that this antagonism was not simply competitive. The apparent pA 2 value for suramin, taken from this Schild plot, was 4.6. 4 Suramin (200–400 μ m ) also noncompetitively inhibited aggregation induced by U46619 (a thromboxane receptor agonist) or by 5‐hydroxytryptamine in the presence of adrenaline (100 μ m ), and caused a depression of the maximal response to these agonists. This nonspecific effect of suramin may explain the high Schild plot slope obtained against ADP. 5 These results provide evidence that the ADP receptor on human platelets is indeed similar to the P 2 ‐purinoceptors responding to adenine nucleotides on smooth muscle and other tissues, and show that suramin cannot distinguish between the proposed subtypes of the P 2 ‐purinoceptors.