Inhibition of platelet aggregation with intravenous and oral administration of carboprostacyclin in man

S.M.M. Karim, P.G. Adaikan, L.C. Lau, M.Y. Tai
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引用次数: 12

Abstract

Intravenous infusion of carboprostacyclin, a chemically stable analogue of prostacyclin (PGI2) resulted in ex-vivo inhibition of ADP-induced platelet aggregation at doses that did not produce significant changes in blood pressure or heart rate. Oral administration of relatively large doses of this compound also inhibited ex-vivo ADP-induced platelet aggregation but this was accompanied by headache, facial flush, tachycardia and changes in blood pressure.

静脉和口服卡前列环素对血小板聚集的抑制作用
静脉输注卡前列环素,一种化学上稳定的前列环素类似物(PGI2),可在体外抑制adp诱导的血小板聚集,剂量不产生显著的血压或心率变化。口服相对大剂量的这种化合物也能抑制体外adp诱导的血小板聚集,但伴有头痛、面部潮红、心动过速和血压变化。
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