Epinephrine at even high concentrations neither caused shape change nor agg
regation of rat platelets. However, epinephrine induced aggregation in the
presence of low (near-threshold) concentrations of collagen at which concen
tration only platelet shape change was induced without aggregation. The pla
telet aggregation was also induced by some other catecholamines and clonidi
ne but not by beta -agonist isoproterenol. The aggregatory potencies of R-(
-)-isomers, (-)-epinephrine and (-)-norepinephrine were higher than the cor
responding desoxy derivatives, epinine and dopamine. In addition, the epine
phrine-induced rat platelet aggregation was inhibited by alpha (2)-antagoni
sts, yohimbin and phentolamine, but not by alpha (1)-antagonist prazosin or
beta -antagonist propranolol. These results suggested that the epinephrine
-induced rat platelet aggregation is occurring through alpha (2)-adrenergic
receptors as is the case with human platelets. (C) 2000 Elsevier Science L
td. All rights reserved.