Zucker M L, Budd S E, Dollar L E, Chernoff S B, Altman R
Department of Pathology, University of Kansas Medical Center, Kansas City.
Thromb Haemost. 1993 Aug 2;70(2):332-5.
The authors studied the effects of diltiazem, administered alone and together with low-dose aspirin, on the platelet response to paired agonists. After a baseline period, 25 healthy volunteers were given oral diltiazem for 1 week (120, 240, or 360 mg/day), and then crossed over randomly between 1 week on diltiazem plus aspirin (81 mg/day), and 1 week on aspirin (81 mg/day) alone. Platelet function was tested on 2 consecutive days in each period. Synergistic platelet aggregation and ATP release were obtained at baseline using a subthreshold concentration of arachidonic acid combined with platelet activating factor, ADP, or epinephrine. Diltiazem resulted in significant decrease from baseline in platelet aggregation and ATP release using the arachidonic acid-epinephrine combination (35% and 40% decrease, respectively, p < 0.01) and a significant decrease in aggregation using the arachidonic acid-ADP combination (22% decrease, p < 0.01). The effects were neither dose-related, nor accompanied by any significant change in serum thromboxane B2 levels or bleeding times. There was no significant difference between the effects of aspirin alone and aspirin plus diltiazem on the synergistic platelet aggregation and ATP release induced by the paired agonists, or on thromboxane B2 levels or bleeding times. Diltiazem administered in vivo partially inhibits the synergistic platelet aggregation and ATP release induced by paired agonists; however, in contrast to a previous in vitro study it does not potentiate the platelet-inhibitory effect of aspirin.
作者研究了单独使用地尔硫䓬以及与小剂量阿司匹林联合使用时,其对血小板对配对激动剂反应的影响。在基线期过后,25名健康志愿者口服地尔硫䓬1周(120、240或360毫克/天),然后随机交叉接受1周的地尔硫䓬加阿司匹林(81毫克/天)治疗,以及1周的单独阿司匹林(81毫克/天)治疗。在每个阶段连续两天检测血小板功能。在基线时,使用亚阈值浓度的花生四烯酸联合血小板激活因子、二磷酸腺苷(ADP)或肾上腺素,可获得协同性血小板聚集和三磷酸腺苷(ATP)释放。使用花生四烯酸 - 肾上腺素组合时,地尔硫䓬导致血小板聚集和ATP释放较基线显著降低(分别降低35%和40%,p < 0.01),使用花生四烯酸 - ADP组合时,聚集显著降低(降低22%,p < 0.01)。这些作用既与剂量无关,也未伴随血清血栓素B2水平或出血时间的任何显著变化。单独使用阿司匹林与阿司匹林加地尔硫䓬对配对激动剂诱导的协同性血小板聚集和ATP释放、血栓素B2水平或出血时间的影响之间,没有显著差异。体内给予地尔硫䓬可部分抑制配对激动剂诱导的协同性血小板聚集和ATP释放;然而,与先前的体外研究相反,它并未增强阿司匹林的血小板抑制作用。