Boeynaems J M, Galand N
Biochem Biophys Res Commun. 1983 Apr 15;112(1):290-6. doi: 10.1016/0006-291x(83)91829-6.
Extracellular ADP and ATP stimulated the synthesis of prostacyclin - as reflected by the release of 6-keto-PGF1 alpha - in the rabbit aorta, the rabbit pulmonary artery and the rat aorta. A doubling of 6-keto-PGF1 alpha output was produced by 3 microM ADP. Adenosine had no effect and the stimulation by ADP was blocked by quinidine, but not by theophylline. This stimulation was abolished by indomethacin and lost after mechanical removal of the endothelium. Stimulation of vascular prostacyclin synthesis by ADP released from aggregating platelets could help localize thrombus formation to areas of vascular damage.
细胞外二磷酸腺苷(ADP)和三磷酸腺苷(ATP)可刺激前列环素的合成,兔主动脉、兔肺动脉和大鼠主动脉中6-酮-前列腺素F1α的释放反映了这一点。3微摩尔ADP可使6-酮-前列腺素F1α的产量加倍。腺苷无此作用,ADP的刺激作用可被奎尼丁阻断,但不能被茶碱阻断。吲哚美辛可消除这种刺激作用,机械去除内皮后刺激作用消失。聚集血小板释放的ADP对血管前列环素合成的刺激作用有助于将血栓形成定位在血管损伤部位。