Lin M S, Huang C S
Department of Medicine and Clinical Pathology, Cathay General Hospital, Taipei, Taiwan.
Int J Clin Pharmacol Ther Toxicol. 1991 Oct;29(10):391-3.
To evaluate the ex-vivo effects of labetalol, at effective vasodepressor doses, on platelet aggregation in hypertension, 30 hypertensive patients were randomized to either a labetalol or control group in a ratio of two to one. For the labetalol group, the dosage was titrated from 400 mg to 600 mg per day to achieve a fall of 10 mmHg in mean arterial pressure (MAP). No drug was used in the control group. The study lasted for 4 to 8 weeks. At the beginning and end of the study, platelet aggregation to collagen, adenosine diphosphate and epinephrine were measured according to Born's method. In contrast to the significant reduction in MAP, platelet aggregation was not altered by labetalol compared with the control group. Our data do not support the hypothesis that labetalol, at effective vasodepressor doses, inhibits platelet aggregation in mild-to-moderate hypertensive patients.
为评估拉贝洛尔在有效血管减压剂量下对高血压患者血小板聚集的体外作用,30例高血压患者按2:1的比例随机分为拉贝洛尔组或对照组。拉贝洛尔组的剂量从每天400毫克滴定至600毫克,以使平均动脉压(MAP)下降10毫米汞柱。对照组未使用任何药物。研究持续4至8周。在研究开始和结束时,根据博恩方法测量血小板对胶原、二磷酸腺苷和肾上腺素的聚集情况。与MAP的显著降低相反,与对照组相比,拉贝洛尔并未改变血小板聚集。我们的数据不支持以下假设:在有效血管减压剂量下,拉贝洛尔可抑制轻至中度高血压患者的血小板聚集。