Takano S, Sakurai K, Suzuki T
Jpn J Pharmacol. 1980 Dec;30(6):905-12. doi: 10.1254/jjp.30.905.
Effects of tiaramide, aspirin an indomethacin were studied on rabbit platelet aggregation in vivo and on platelet electrophoretic mobility. When tiaramide (6 mg/kg), aspirin (30 mg/kg) or indomethacin (1.3 mg/kg) was injected into the ear vein of rabbit during 60 sec, tiaramide only inhibited ADP-induced aggregation, 20 min after the injection. All three drugs prevented collagen-induced aggregation 20 and 120 min after the injection. Tiaramide and aspirin prevented aggregation 24 hours later. The inhibitory effects on the aggregation of tiaramide are presumably independent of prostaglandin synthesis, because malondialdehyde (a metabolite of PGG2) production was not influenced. Tiaramide reduced cyclic AMP levels in platelets after 20 min incubation, despite the ability of this agent to inhibit platelet aggregation. Tiaramide, aspirin and indomethacin per se has no effect on platelet electrophoretic mobility, while tiaramide prevented the decrease in the mobility produced by ADP. Tiaramide and aspirin also depressed the decrease in the mobility produced by collagen.
研究了替拉米特、阿司匹林和吲哚美辛对家兔体内血小板聚集及血小板电泳迁移率的影响。当在60秒内将替拉米特(6毫克/千克)、阿司匹林(30毫克/千克)或吲哚美辛(1.3毫克/千克)注入家兔耳静脉时,仅替拉米特在注射后20分钟抑制ADP诱导的聚集。注射后20分钟和120分钟,这三种药物均能阻止胶原诱导的聚集。替拉米特和阿司匹林在24小时后仍能阻止聚集。替拉米特对聚集的抑制作用可能与前列腺素合成无关,因为丙二醛(PGG2的代谢产物)的生成未受影响。尽管替拉米特具有抑制血小板聚集的能力,但孵育20分钟后它会降低血小板中的环磷酸腺苷水平。替拉米特、阿司匹林和吲哚美辛本身对血小板电泳迁移率无影响,而替拉米特可阻止ADP引起的迁移率降低。替拉米特和阿司匹林还能抑制胶原引起的迁移率降低。