Rodrigues M, Fitscha P, Sinzinger H
Department of Nuclear Medicine, University of Vienna, Austria.
J Physiol Pharmacol. 1994 Dec;45(4):533-9.
The PGI2/NO axis is well accepted for its central regulatory role in maintaining haemostatic balance in large arteries. Earlier findings suggest that PGD2 may also play a role in haemostatic regulation of human cerebral circulation. We therefore wondered whether PGD2 and its metabolite PGJ2 synergise in-vitro with NO. We approached this question using platelets of ten healthy donors and ADP as aggregation-inducing stimulus. Both PGD2 and PGJ2 do inhibit ADP-induced platelet aggregation in a dose-dependent manner. Platelet aggregation findings demonstrate that PGD2 and NO synergise, as does the metabolite PGJ2. Our data are indicative that the PGD2/NO and, in less extent, PGJ2/NO synergism might be of special importance for the cerebrovascular haemostatic control.
前列环素2/一氧化氮轴因其在维持大动脉止血平衡中的核心调节作用而被广泛认可。早期研究结果表明,前列腺素D2可能也在人类脑循环的止血调节中发挥作用。因此,我们想知道前列腺素D2及其代谢产物15-脱氧-Δ12,14-前列腺素J2(PGJ2)在体外是否与一氧化氮协同作用。我们使用来自十名健康供体的血小板和二磷酸腺苷(ADP)作为聚集诱导刺激物来探讨这个问题。前列腺素D2和PGJ2均以剂量依赖性方式抑制ADP诱导的血小板聚集。血小板聚集结果表明,前列腺素D2和一氧化氮协同作用,其代谢产物PGJ2也是如此。我们的数据表明,前列腺素D2/一氧化氮以及在较小程度上PGJ2/一氧化氮的协同作用可能对脑血管止血控制具有特殊重要性。