Regulatory role of cyclic adenosine 3′,5′-monophosphate on the plattelet cyclooxygenase and platelet function |
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Authors: | Francis A Fitzpatrick Robert R Gorman |
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Institution: | Pharmaceutical Research and Development, The Upjohn Company, Kalamazoo, MI 49001 U.S.A. |
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Abstract: | Thromboxane A2 plays and important role in arachidonic acid- and prostaglandin H2-induced platelet aggregation. Agents that stimulate platelet adenylate cyclase (prostaglandin I2, prostaglandin I1, and prostaglandin E1) and dibutyryl cyclic AMP inhibit both thromboxane A2 formation and arachidonate-induced aggregation platelet-rich plasma. Despite complete suppression of aggregation with agents that elevate cyclic AMP, considerable thromboxane A2 is still formed. Prostaglandin H2-induced aggregations which bypass the cyclooxygenase regulatory step are also inhibited by agents that elevate cyclic AMP without any measurable effect on thromboxane A2 production. These data demonstrate that cyclic AMP can inhibit platelet aggregation by a mechanism independent of its ability to suppress the cycyooxygenase enzyme. Parallel experiments with washed platelet preparations suggest that they may be an inadequate mode for studying relationship between the platelet cyclooxygenase and platelet function. |
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Keywords: | Cyclic AMP Prostaglandin Platelet aggregation Cyclooxygenase HHT 12L-hydroxy-8 10-heptadecadienoic acid PBSG phosphate-buffered saline with gelatin |
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