Brief Review Mediators Produced by the Endothelial Cell

This review discusses the role of three mediators, synthesized by vascular endotheiial cells, that help to keep the surface of the normal endotheliuin nonthrombogenic. The first is prostacydin, a product of arachldonic add metabolism discovered hi 1976. This labile prostanoid, with a half-life of approximately 3 minutes, relaxes vascular smooth musde and inhibits the aggregation of blood platelets. Prostacydin and its analogues are currently being tested clinically for use hi cardiovascular diseases such as primary pulmonary hypertension. The second mediator discussed is endothelium-derived relaxing factor (EDRF), discovered in 1980, which also relaxes smooth muscle and inhibits the aggregation and adhesion of platelets. Substances that stimulate the release of EDRF include acetykhoUne, bradykinin, and adenosine 5'-diphosphate. EDRF is even more labile than prostacydin, with a half-life of about 6 seconds, and it has recently been identified as nitric oxide. Prostacydin and EDRF are released together following stimulation of endothelial receptors and synergize to inhibit platelet aggregation. 13-Hydroxy9,11-octadecadienoic add, a third suggested mediator, is not released but acts from inside the cell to make the endothelial surface nonadhesive for circulating blood ceils. It is proposed that these three mediators form the endothelial defense mechanism against blood-borne cells and chemicals and that breakdown of this barrier results in diseases such as hypertension and atherosclerosis. (Hypertension 12: 530-548,1988)