The antiarrhythmic and cardioprotective drug stobadine, possessing antioxid
ant and neuroprotective properties, was studied as to its in vitro effect o
n aggregation of human blood platelets. Pretreatment of platelets with stob
adine for 30 s inhibited stimulated platelet aggregation in a dose-dependen
t way. Depending on the aggregation stimulus used, the minimal effective co
ncentrations of the drug were 1 mu mol/l (adrenaline), 200 mu mol/l (ADP),
and 1,000 mu mol/l (PMA). Aggregation induced with thrombin or Ca2+-ionopho
re A23187 was not changed in the presence of stobadine even in the concentr
ation of 1,000 mu mol/l. Addition of stobadine 30 s after adrenaline was al
so effective and terminated aggregation (100 and 1,000 mu mol/l) or prolong
ed onset of its second phase (10 mu mol/l). The presented experiments showe
d stobadine as a potent inhibitor of adrenaline-induced aggregation, indica
ting its involvement in the observed antithrombotic and cytoprotective acti
vity.