Vinge E
Eur J Clin Pharmacol. 1985;28(2):163-9. doi: 10.1007/BF00609686.
A single oral dose of indomethacin 1 mg/kg was given to 6 male and 6 female volunteers. The formation of thromboxane B2 (TXB2) and 6-keto-prostaglandin F1 alpha (6-keto-PGF1 alpha) in clotting whole blood was measured by radioimmunoassay, and platelet aggregation induced by arachidonic acid (AA) was measured with a plasma aggregometer. The results were related to the concomitant plasma concentration of indomethacin. The maximum plasma concentration ranged between 3.24 and 8.11 micrograms/ml and the elimination half-life between 4 and 11 h. Formation of the prostanoids was reversibly inhibited, with maximum suppression when the drug concentration in plasma exceeded 0.5-1.0 microgram/ml; the IC50 was approximately 0.1 microgram/ml. Platelet aggregation was also reversibly inhibited. The correlation between the formation of prostanoids and the different phases of the aggregatory response to exogenous AA is discussed.
给6名男性和6名女性志愿者口服单剂量1毫克/千克的吲哚美辛。通过放射免疫分析法测定凝血全血中血栓素B2(TXB2)和6-酮-前列腺素F1α(6-酮-PGF1α)的生成情况,并用血浆凝集仪测定花生四烯酸(AA)诱导的血小板聚集情况。将结果与吲哚美辛的血浆浓度进行关联。血浆最大浓度在3.24至8.11微克/毫升之间,消除半衰期在4至11小时之间。前列腺素的生成受到可逆性抑制,当血浆中药物浓度超过0.5 - 1.0微克/毫升时抑制作用最大;半数抑制浓度(IC50)约为0.1微克/毫升。血小板聚集也受到可逆性抑制。讨论了前列腺素生成与对外源性AA聚集反应不同阶段之间的相关性。