Summary
The antithrombotic effect of MCI-9042, (±)-2-(dimethylamino)-1-[[o-(m-methoxyphenethyl)phenoxy] methyl] ethyl hydrogen succinate hydrochloride was investigated
in three different experimental thrombosis models in animals. Simultaneous injection
of serotonin and collagen into the tail vein in mice induced acute pulmonary thromboembolic
death. MCI-9042 reduced the mortality in a dose dependent manner and its ED50 value was 1.9 mg/kg po. Ticlopidine (TCP) which is a positive reference compound
as an antithrombotic drug reduced the mortality at doses of 10 mg/kg po and above.
Cyproheptadine (CPH) and ketanserin (KTS) which are S2-serotonergic antagonists were
also effective on the reduction of mortality. In mesenteric arterial thrombosis induced
by electric stimulation in mice, MCI-9042 prolonged the occlusion time resulted from
platelet thrombus formation (PD50: 23 mg/kg po). CPH and KTS prolonged the occlusion time as potent as MCI-9042, but
TCP prolonged the occlusion time only at the high doses of 100 mg/kg po and above.
In experimental arterial thrombosis which generated in implanted polyethylene tubing,
MCI-9042 reduced the incidence of thrombus formation in the tubing and its ED50 value was 18 mg/kg po. TCP was also effective in this model with an ED50 of 170 mg/kg po. The present results lead to the consideration that serotonin plays
a more important role in thrombus formation than that conjectured formerly, and suggest
that MCI-9042 becomes a new kind of antithrombotic drug with S2-serotonergic receptor antagonism.
