Halushka P V
Department of Cell and Molecular, Medical University of South Carolina, Charleston.
Z Kardiol. 1989;78 Suppl 3:42-7.
Thromboxane A2 and its immediate precursor, prostaglandin H2, induce platelet aggregation and constriction of vascular and bronchial smooth muscle. These effects are mediated through specific membrane receptors. Since these compounds have the same pharmacologic properties they are thought to share a common receptor that has been named thromboxane A2/prostaglandin H2. Evidence has accumulated in the last few years supporting the hypothesis that the platelet and vascular receptors are different. The platelet receptor has been tentatively named [TXA2/PGH2]alpha, alpha for aggregation and the vascular receptor (TXA2/PGH2]tau, tau for tone. In recent years there have been many thromboxane A2 receptor antagonists synthesized and some are now in various stages of clinical development. Based on many preclinical and some clinical studies, it appears that these drugs may prove to be of significant therapeutic benefit in a variety of cardiovascular and renal diseases.
血栓素A2及其直接前体前列腺素H2可诱导血小板聚集以及血管和支气管平滑肌收缩。这些作用是通过特定的膜受体介导的。由于这些化合物具有相同的药理特性,因此人们认为它们共享一种共同的受体,该受体被命名为血栓素A2/前列腺素H2。在过去几年中积累的证据支持血小板受体和血管受体不同这一假说。血小板受体被暂定为[TXA2/PGH2]α,α代表聚集,而血管受体为[TXA2/PGH2]τ,τ代表张力。近年来,已经合成了许多血栓素A2受体拮抗剂,其中一些目前正处于临床开发的各个阶段。基于许多临床前和一些临床研究,这些药物似乎可能在多种心血管和肾脏疾病中证明具有显著治疗益处。