At concentrations ranging from 10(-9) to 10(-6) M, trilinolein inhibit
ed epinephrine-induced platelet aggregation. This inhibition was accom
panied by reduced ATP release and thromboxane B-2 formation. However,
concentration-response curves for the interaction between trilinolein
and epinephrine showed that trilinolein was unlikely a competitive ant
agonist of epinephrine. Platelet aggregation induced by collagen, thro
mbin, ADP or arachidonic acid was not inhibited. This study supported
the theory that this type of triglyceride may have therapeutic potenti
al but the definite mechanism for its effect remains to be answered.