Abstract
Platelet-derived cyclooxygenase products are intimately involved in two types of local platelet-vessel wall interactions: Regulation of hemostasis and control of vessel tone. This paper reviews the possible theoretical and clinical benefits of selective pharmacological interference with platelet-derived cyclooxygenase products by thromboxane synthase inhibitors, blockers of PGH2/TXA2 receptors and combined-mode compounds in comparison with acetylsalicylic acid (aspirin). It is concluded that low-dose aspirin is safe and effective to reduce the thromboembolic risk in high-risk cardiovascular patients. However, the low selectivity of the compound for different cyclooxygenases and the high sensitivity of the platelet enzyme might result in suppressed vascular PGI2 formation. Agents, interfering more selectively with thromboxane formation and/or action, do not suppress vascular PGI2 generation but usually are reversible-type antagonists with limited clinical experience. Fresh insights into transcellular precursor exchange and the regulation and function of thromboxane receptors might result in the development of new promising compounds in the future.
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Schrör, K. (1991). Pharmacological Modification of Platelet-Derived Cyclooxygenase Product Formation and Its Consequences for Platelet-Vessel Wall Interactions. In: Herman, A.G. (eds) Antithrombotics. Developments in Cardiovascular Medicine, vol 126. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3484-2_8
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