Jeremy J Y, Mikhailidis D P, Dandona P
Eur J Pharmacol. 1985 Jan 2;107(2):259-62. doi: 10.1016/0014-2999(85)90066-4.
Since platelet release reaction products (e.g. serotonin, ADP) stimulate prostacyclin (PGI2) release in vitro, we have investigated whether thromboxane A2 (TXA2) also has a similar effect. An analogue, U-46619, was used for the experiments, since TXA2 is extremely unstable. U-46619 stimulated rat aortic PGI2 release; this stimulation was abolished by (a) EDTA and (b) verapamil. We conclude that TXA2 is a calcium-dependent stimulator of PGI2 release; this property may be relevant to the limitation of platelet aggregates in vivo and to vascular injury.
由于血小板释放反应产物(如5-羟色胺、二磷酸腺苷)在体外能刺激前列环素(PGI2)释放,我们研究了血栓素A2(TXA2)是否也有类似作用。由于TXA2极不稳定,实验中使用了其类似物U-46619。U-46619刺激大鼠主动脉释放PGI2;这种刺激可被(a)乙二胺四乙酸(EDTA)和(b)维拉帕米消除。我们得出结论,TXA2是PGI2释放的钙依赖性刺激物;这一特性可能与体内血小板聚集体的限制及血管损伤有关。