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Experimental & Molecular Medicine ; : 42-46, 1999.
Article in English | WPRIM | ID: wpr-186198

ABSTRACT

Our previous studies have shown that subthreshold concentrations of two platelet agonists exert synergistic effects on platelet aggregation. Here we studied the mechanism of synergistic interaction of 5-hydroxytryptamine (5-HT) and epinephrine mediated platelet aggregation. We show that 5-HT had no or little effect on aggregation but it did potentiate the aggregation response of epinephrine. The synergistic interaction of 5-HT (1-5 microM) and epinephrine (0.5-2 microM) was inhibited by alpha2-adrenoceptor blocker (yohimbine; IC50= 0.4 microM), calcium channel blockers (verapamil and diltiazem with IC50 of 10 and 48 mM, respectively), PLC inhibitor (U73122; IC50=6 microM) and nitric oxide (NO) donor, SNAP (IC50=1.6 microM)). The data suggest that synergistic effects of platelet agonists are receptor-mediated and occur through multiple signalling pathways including the activation PLC/Ca2+ signalling cascades.


Subject(s)
Humans , Blotting, Western , Calcium Channel Blockers/pharmacology , Calcium Signaling , Drug Synergism , Enzyme Activation , Enzyme Inhibitors/pharmacology , Epinephrine/pharmacology , GTP-Binding Protein alpha Subunits, Gi-Go/metabolism , GTP-Binding Proteins/metabolism , Type C Phospholipases/metabolism , Type C Phospholipases/antagonists & inhibitors , Platelet Aggregation/physiology , Platelet Aggregation/drug effects , Serotonin/pharmacology , Signal Transduction
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