Involvement of 5HT2 receptors in human platelet aggregation was assess
ed by studying the effect of ADP, epinephrine and thrombin on H-3-5HT
release from platelets. The release experiments were made with a perfu
sion method to preserve any compound, released or formed by platelet,
from interacting with platelet itself. In these conditions, aggregatio
n does not occur, as confirmed by Scanning Electron Microscopy. These
release experiments showed that the platelet activation by such agents
is coupled with 5-HT release. The aggregation experiments, made on di
fferent aliquots of the same platelet-rich plasma (PRP), showed that t
he released 5-HT, interacting with its own receptors on platelet activ
ated surface, determines aggregation. In fact, although it is known th
at 5-HT added to PRP was only able to induce a moderate platelet aggre
gation, the 5-HT2 antagonist ketanserin counteracted the aggregation i
nduced by ADP, epinephrine and thrombin. These results suggest that a
5HT2 antagonist could be therapeutically important in those pathologic
al states in which serotonin, released by activated platelets, may inc
rease aggregation.