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抗心律失常药物维拉帕米和丙吡胺对血小板功能的抑制作用。

Inhibition of platelet function of antiarrhythmic drugs, verapamil and disopyramide.

作者信息

Han P, Boatwright C, Ardlie N G

出版信息

Thromb Haemost. 1982 Apr 30;47(2):150-3.

PMID:7101234
Abstract

Various cardiovascular drugs such as nitrates and propranolol, used in the treatment of coronary artery disease have been shown to have an antiplatelet effect. We have studied the in vitro effects of two antiarrhythmic drugs, verapamil and disopyramide, and have shown their inhibitory effect on platelet function. Verapamil, a calcium channel blocker, inhibited the second phase of platelet aggregation induced by adenosine diphosphate (*ADP) and inhibited aggregation induced by collagen. Disopyramide similarly inhibited the second phase of platelet aggregation caused by ADP and aggregation induced by collagen. Either drug in synergism with propranolol inhibited ADP or collagen-induced platelet aggregation. Disopyramide at high concentrations inhibited arachidonic acid whereas verapamil was without effect. Verapamil, but not disopyramide, inhibited aggregated induced by the ionophore A23187.

摘要

用于治疗冠状动脉疾病的各种心血管药物,如硝酸盐和普萘洛尔,已被证明具有抗血小板作用。我们研究了两种抗心律失常药物维拉帕米和丙吡胺的体外作用,并证明了它们对血小板功能的抑制作用。维拉帕米是一种钙通道阻滞剂,它抑制由二磷酸腺苷(ADP)诱导的血小板聚集的第二阶段,并抑制由胶原诱导的聚集。丙吡胺同样抑制由ADP引起的血小板聚集的第二阶段以及由胶原诱导的聚集。这两种药物中的任何一种与普萘洛尔协同作用时,都能抑制ADP或胶原诱导的血小板聚集。高浓度的丙吡胺抑制花生四烯酸,而维拉帕米则无此作用。维拉帕米能抑制由离子载体A23187诱导的聚集,而丙吡胺则不能。

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