TY - JOUR
T1 - Antiplatelet effects of oral diltiazem, propranolol, and their combination.
AU - Ring, ME
AU - Corrigan, JJ
AU - Fenster, PE
PY - 1987/11
Y1 - 1987/11
N2 - 1. The antiplatelet effects of a single oral dose of the calcium entry blocker diltiazem (60 mg), the beta‐adrenoceptor blocker propranolol (40 mg), and their combination were studied in five healthy subjects. 2. Platelet aggregation and ATP release induced by adrenaline and ADP and ADP induced platelet thromboxane A2 generation were significantly inhibited (P less than 0.05) by either diltiazem or propranolol, although propranolol tended to have greater inhibitory effects on platelet function than diltiazem that did not reach statistical significance. 3. Combination therapy resulted in additive antiplatelet effects that were significantly (P less than 0.05) greater than either drug alone. 4. These data indicate that combined administration of a calcium entry blocker and a beta‐adrenoceptor blocker results in additive inhibitory effects on platelet function. These effects may mediate part of the therapeutic efficacy of combination therapy in patients with coronary artery disease. 1987 The British Pharmacological Society
AB - 1. The antiplatelet effects of a single oral dose of the calcium entry blocker diltiazem (60 mg), the beta‐adrenoceptor blocker propranolol (40 mg), and their combination were studied in five healthy subjects. 2. Platelet aggregation and ATP release induced by adrenaline and ADP and ADP induced platelet thromboxane A2 generation were significantly inhibited (P less than 0.05) by either diltiazem or propranolol, although propranolol tended to have greater inhibitory effects on platelet function than diltiazem that did not reach statistical significance. 3. Combination therapy resulted in additive antiplatelet effects that were significantly (P less than 0.05) greater than either drug alone. 4. These data indicate that combined administration of a calcium entry blocker and a beta‐adrenoceptor blocker results in additive inhibitory effects on platelet function. These effects may mediate part of the therapeutic efficacy of combination therapy in patients with coronary artery disease. 1987 The British Pharmacological Society
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U2 - 10.1111/j.1365-2125.1987.tb03220.x
DO - 10.1111/j.1365-2125.1987.tb03220.x
M3 - Article
C2 - 3435691
AN - SCOPUS:0023589244
SN - 0306-5251
VL - 24
SP - 615
EP - 620
JO - British Journal of Clinical Pharmacology
JF - British Journal of Clinical Pharmacology
IS - 5
ER -