乌拉地尔对体外血小板对肾上腺素和其他聚集剂反应的影响

Emanuelli G. , Anfossi G. , Lanzio M. , Mularoni E. , Calcamuggi G. , Brunello F. , Busca G.P. , Ciani D.
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引用次数: 6

摘要

观察降压药乌拉地尔对人血小板功能的影响。乌拉地尔未能证明直接的聚集特性或增强作用。此外,高浓度药物抑制血小板对ADP、PAF、胶原、肾上腺素和牛凝血酶的反应,影响ADP和PAF诱导的血小板释放反应。数据表明,乌拉地尔对人血小板α 2-肾上腺素受体具有可忽略不计的激动作用,并且在高浓度时干扰血小板活化,其他抗聚集化合物也证明了这一点。
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Influence of urapidil on in vitro platelet response to adrenaline and other aggregating agents

The effects of hypotensive drug urapidil on human platelet functions were investigated.

Urapidil failed to evidence direct aggregating properties or potentiating effects. Furthermore, drug high concentrations inhibited the platelet response to ADP, PAF, collagen, adrenaline and bovine thrombin, and influenced the platelet release reaction induced by ADP and PAF.

Data indicate that urapidil possesses negligible agonistic effects on human platelet alpha 2-adrenoceptors and interferes at high concentrations with the platelet activation, as evidenced for other anti-aggregating compounds.

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