Yui Y, Takatsu Y, Hattori R, Kawai C, Osaki Y, Yohida T
Jpn Circ J. 1985 Jun;49(6):571-5. doi: 10.1253/jcj.49.571.
Effects of a new stable prostacyclin analogue OP41483 (15-cyclopentyl-omega-pentanor-5(E)-carbacyclin) on platelet aggregation, plasma thromboxane B2 levels, hemodynamic parameters, and clinical safety were studied. Normal volunteers received intravenous infusions of OP41483 at doses of 2.5 (n = 3), 5.0 (n = 3), 10 (n = 3), and 20 (n = 5) ng/kg/min for one hour. During infusion, ADP (adenosine diphosphate)-induced platelet aggregation decreased significantly, and blood pressure decreased slightly, but plasma thromboxane B2 levels did not change significantly. The intravenous infusion of OP41483 at the dose of 10 ng/kg/min for one hour over three successive days was performed. During the each infusion, platelet aggregation and mean blood pressure decreased significantly.
研究了一种新型稳定的前列环素类似物OP41483(15-环戊基-ω-五降-5(E)-卡前列环素)对血小板聚集、血浆血栓素B2水平、血流动力学参数和临床安全性的影响。正常志愿者分别以2.5(n = 3)、5.0(n = 3)、10(n = 3)和20(n = 5)ng/kg/min的剂量静脉输注OP41483,持续1小时。输注期间,二磷酸腺苷(ADP)诱导的血小板聚集显著降低,血压略有下降,但血浆血栓素B2水平无显著变化。连续三天每天以10 ng/kg/min的剂量静脉输注OP41483 1小时。每次输注期间,血小板聚集和平均血压均显著降低。