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Thrombin‐Induced Platelet Prostaglandin and Cyclic AMP Production and a Possible Intrinsic Modulation of Platelet Function *
Author(s) -
DROLLER MICHAEL J.
Publication year - 1976
Publication title -
scandinavian journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0036-553X
DOI - 10.1111/j.1600-0609.1976.tb01172.x
Subject(s) - platelet , radioimmunoassay , thrombin , chemistry , extracellular , endocrinology , medicine , calcium , cyclic nucleotide , intracellular , secretion , prostaglandin , nucleotide , prostaglandin e , calcium in biology , biochemistry , biology , gene
In previous studies, we observed an increase in intracellular cyclic AMP in platelets during thrombin‐induced nucleotide and calcium release. Our present work suggests that platelet prostaglandins are directly involved in this phenomenon. Washed human platelets were incubated at 37°C with human thrombin for times ranging between 5 s and 5 min. The release of nucleotides and calcium in response to thrombin, determined spectrophotometrically, reached 40–60% of maximal plateau levels by 5 s, 70–80% by 10 s, and 90–100% by 15 s. The production and secretion of prostaglandin E (PGE), measured by radioimmunoassay, parelleled this rapid time course. After 10 s, however, the amount of extracellular PGE began to decrease, continuing to do so through 5 min of incubation. Intracellular cyclic AMP accumulation, determined by radioimmunoassay, lagged behind the time course of nucleotide and calcium release, and that of PGE secretion, by several seconds. This lag in cyclic AMP accumulation appeared to correlate closely with the disappearance of PGE from the supernate in the same platelet samples. In view of the inhibitory effects of cyclic AMP and PGE on platelet release and aggregation, these interrelated time course curves suggest the existence within platelets of a mechanism for the modulation of platelet activity.