Pengo V, Boschello M, Marzari A, Baca M, Schivazappa L, Dalla Volta S
Thromb Haemost. 1986 Oct 21;56(2):147-50.
A brief contact between native whole blood and ADP promotes a dose-dependent release of platelet alpha-granules without a fall in the platelet number. We assessed the "ex vivo" effect of three widely used antiplatelet drugs, aspirin dipyridamole and ticlopidine, on this system. Aspirin (a single 800 mg dose) and dipyridamole (300 mg/die for four days) had no effect, while ticlopidine (500 mg/die for four days) significantly reduced the alpha-granules release for an ADP stimulation of 0.4 (p less than 0.02), 1.2 (p less than 0.01) and 2 microM (p less than 0.01). No drug, however, completely inhibits this early stage of platelet activation. The platelet release of alpha-granules may be related to platelet shape change of the light transmission aggregometer and may be important "in vivo" by enhancing platelet adhesiveness and by liberating the platelet-derived growth factor.
天然全血与二磷酸腺苷(ADP)短暂接触可促进血小板α颗粒呈剂量依赖性释放,而血小板数量并不减少。我们评估了三种广泛使用的抗血小板药物阿司匹林、双嘧达莫和噻氯匹定对该系统的“体外”作用。阿司匹林(单次800毫克剂量)和双嘧达莫(每日300毫克,共四天)无作用,而噻氯匹定(每日500毫克,共四天)在ADP刺激浓度为0.4微摩尔(p<0.02)、1.2微摩尔(p<0.01)和2微摩尔(p<0.01)时,可显著减少α颗粒释放。然而,没有一种药物能完全抑制血小板激活的这一早期阶段。血小板α颗粒的释放可能与透光率聚集仪检测的血小板形状改变有关,并且通过增强血小板黏附性和释放血小板衍生生长因子,可能在“体内”发挥重要作用。