Pamphilon D H, Boon R J, Prentice A G, Rozkovec A
Department of Haematology, Derriford Hospital, Plymouth.
J Clin Pathol. 1989 Aug;42(8):793-6. doi: 10.1136/jcp.42.8.793.
Propranolol, a non-selective beta blocker, was administered orally in therapeutic doses. The effects of a single dose (160 mg) and one week's treatment (80 mg twice a day) on platelet function were compared in healthy young subjects. There were no significant changes in circulating platelet aggregates, template bleeding time, platelet factor 3 availability and thromboxane beta 2 (TX beta 2) generation. Platelet aggregation responses as assessed by angle of slope and maximal percentage aggregation (all agonists) and lag phase (collagen) showed no changes of biological importance, although minor changes reaching significance were observed with some agonists. These findings suggest that propranolol does not significantly affect platelet function when taken at doses commonly encountered in clinical practice.
普萘洛尔,一种非选择性β受体阻滞剂,以治疗剂量口服给药。在健康年轻受试者中比较了单次剂量(160毫克)和一周治疗(每天两次,每次80毫克)对血小板功能的影响。循环血小板聚集体、模板出血时间、血小板因子3活性和血栓素β2(TXβ2)生成均无显著变化。通过斜率角度、最大聚集百分比(所有激动剂)和延迟期(胶原蛋白)评估的血小板聚集反应未显示具有生物学意义的变化,尽管使用某些激动剂观察到有达到显著水平的微小变化。这些发现表明,普萘洛尔在临床实践中常用剂量下服用时不会显著影响血小板功能。