Institute of Biotechnology, Molecular Cell Biology, Brandenburg University of Technology, 01968 Senftenberg, Germany.
Int J Mol Sci. 2020 Nov 27;21(23):9020. doi: 10.3390/ijms21239020.
Prostanoids are bioactive lipid mediators and take part in many physiological and pathophysiological processes in practically every organ, tissue and cell, including the vascular, renal, gastrointestinal and reproductive systems. In this review, we focus on their influence on platelets, which are key elements in thrombosis and hemostasis. The function of platelets is influenced by mediators in the blood and the vascular wall. Activated platelets aggregate and release bioactive substances, thereby activating further neighbored platelets, which finally can lead to the formation of thrombi. Prostanoids regulate the function of blood platelets by both activating or inhibiting and so are involved in hemostasis. Each prostanoid has a unique activity profile and, thus, a specific profile of action. This article reviews the effects of the following prostanoids: prostaglandin-D (PGD), prostaglandin-E, -E and E (PGE, PGE, PGE), prostaglandin F (PGF), prostacyclin (PGI) and thromboxane-A (TXA) on platelet activation and aggregation via their respective receptors.
前列腺素是生物活性脂质介质,参与几乎每个器官、组织和细胞中的许多生理和病理生理过程,包括血管、肾脏、胃肠道和生殖系统。在这篇综述中,我们重点关注它们对血小板的影响,血小板是血栓形成和止血的关键因素。血小板的功能受血液和血管壁中的介质影响。激活的血小板聚集并释放生物活性物质,从而激活相邻的血小板,最终可能导致血栓形成。前列腺素通过激活或抑制来调节血小板的功能,因此参与止血。每种前列腺素都具有独特的活性谱,因此具有特定的作用谱。本文综述了以下前列腺素对血小板激活和聚集的影响:前列腺素 D(PGD)、前列腺素 E、E 和 E(PGE、PGE、PGE)、前列腺素 F(PGF)、前列环素(PGI)和血栓素 A(TXA)通过各自的受体。