Nuotto E, Gordin A, Paasonen M K, Metsä-Ketelä T, Lamminsivu U
Eur J Clin Pharmacol. 1983;25(3):313-7. doi: 10.1007/BF01037940.
The effect of acetylsalicylic acid (ASA) on plasma thromboxane A2 (TXA2) and platelet aggregation was studied in 12 healthy, non-smoking, male students, in a double-blind, cross-over study, after single doses and 14-days on ASA 50, 100, 250 and 1000 mg/day. Platelet production of TXA2 was assessed by measuring the thromboxane B2 (TXB2) content of clotted venous blood by RIA. Platelet aggregation induced by ADP and adrenaline was studied by the method of Born. All doses of ASA completely suppressed the production of TXB2 within 3 h, with the exception of the 50 mg dose, which effected only 61% suppression (p less than 0.001). After administration for 14 days the suppression was complete, even including the lowest dose. At that time ASA had blocked the secondary phase of adrenaline- and ADP-induced platelet aggregation. It is concluded that the maximal antithromboxane and antiaggregatory effects, which last for at least 24 h, can be achieved by continuous daily administration of ASA 50 mg.
在一项双盲交叉研究中,对12名健康、不吸烟的男性学生进行了研究,观察单剂量及每天服用50、100、250和1000毫克阿司匹林(ASA)14天后,乙酰水杨酸对血浆血栓素A2(TXA2)和血小板聚集的影响。通过放射免疫分析法(RIA)测定凝血静脉血中血栓素B2(TXB2)的含量,评估血小板TXA2的生成。采用Born法研究二磷酸腺苷(ADP)和肾上腺素诱导的血小板聚集。除50毫克剂量仅抑制61%(p<0.001)外,所有剂量的ASA在3小时内均完全抑制TXB2的生成。服用14天后,抑制作用完全,即使是最低剂量也是如此。此时,ASA已阻断肾上腺素和ADP诱导的血小板聚集的第二阶段。结论是,通过每天持续服用50毫克ASA,可实现持续至少24小时的最大抗血栓素和抗聚集作用。