Why the study?
Does dipyridamole alone or in combination with various doses of acetylsalicylic acid alter the balance between prostacyclin and thromboxane in healthy human subjects?
Does dipyridamole alone or in combination with various doses of acetylsalicylic acid alter the balance between prostacyclin and thromboxane in healthy human subjects?
The anti-thrombotic effect of dipyridamole in vivo does not appear to be mediated through direct changes in PGI2 and/or TxA2 production, while low-dose ASA effectively inhibits TxB2 production.
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Low-dose ASA-dipyridamole improves TxB2/PGI2 ratio without suppressing PGI2; challenges direct eicosanoid mediation of dipyridamole antithrombotic action.
1 Thirty-six healthy human subjects were randomly divided into six groups which were treated with a single dose of 75 mg (1.3 mg/kg) of dipyridamole alone, or 75 mg of dipyridamole in combination with 30 mg (0.5 mg/kg), 50 mg (0.8 mg/kg), 160 mg (2.6 mg/kg) and 330 mg (5.7 mg/kg) of acetylsalicylic acid (ASA), or with placebo. 2 The concentrations of prostacyclin (PGI2) and thromboxane A2 (TxA2) metabolites, 6-keto-prostaglandin F1 alpha (6-keto-PGF1 alpha) and TxB2 respectively, were measured in serum with specific radioimmunoassays before and 1 and 3 h afer the ingestion of the test dose. 3 The basal concentrations of 6-keto-PGF1 alpha and TxB2 correlated significantly (r = 0.588, P less than 0.001). 4 Dipyridamole alone did not change PGI2 or TxA2 production. 5 Dipyridamole-ASA combinations with ASA doses between 0.5 and 0.8 mg/kg inhibited TxB2 production by 48 to 74% and with the ASA doses between 2.6 and 5.7 mg/kg by about 90%. None of these combinations changed PGI2 production. 6 The ratio of 6-keto-PGF1 alpha to TxB2 increased 3.5 to 6 times with ASA doses of 0.5 to 0.8 mg/kg and 21 to 29 times with doses between 2.6 to 5.7 mg/kg. 7 These results suggest that the anti-thrombotic effect of dipyridamole in vivo is not mediated through direct changes in PGI2 and/or TxA2 production.
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Viinikka et al. (1981) studied this question.
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