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双嘧达莫和阿司匹林对全血中血小板聚集的抑制作用。

Inhibition of platelet aggregation in whole blood by dipyridamole and aspirin.

作者信息

Heptinstall S, Fox S, Crawford J, Hawkins M

出版信息

Thromb Res. 1986 Apr 15;42(2):215-23. doi: 10.1016/0049-3848(86)90297-5.

Abstract

We have examined the effects of dipyridamole on platelet aggregation in whole blood both in vitro and after administration to man. The effects of dipyridamole ex vivo were compared with those of aspirin and a combination of dipyridamole and aspirin. In vitro dipyridamole was most effective as an inhibitor of platelet aggregation induced by platelet activating factor (PAF) and low concentrations of arachidonic acid (AA). Its inhibitory effect was always potentiated by adenosine suggesting that its effect on aggregation may be via inhibition of adenosine uptake into blood cells. Ex vivo, dipyridamole, aspirin and the combination of these drugs inhibited the platelet aggregation induced by PAF and AA. Again, adenosine increased the degree of inhibition. These results stress the importance of measuring platelet aggregation in the natural whole blood environment for detection of the inhibitory effects of dipyridamole and suggest a mode of action for the drug.

摘要

我们研究了双嘧达莫对全血中血小板聚集的影响,包括体外实验以及对人体给药后的情况。将双嘧达莫的体外效应与阿司匹林以及双嘧达莫和阿司匹林联合用药的效应进行了比较。在体外,双嘧达莫作为血小板活化因子(PAF)和低浓度花生四烯酸(AA)诱导的血小板聚集抑制剂最为有效。腺苷总是能增强其抑制作用,提示其对聚集的作用可能是通过抑制腺苷摄取进入血细胞。在体外实验中,双嘧达莫、阿司匹林以及这两种药物的联合用药均抑制了PAF和AA诱导的血小板聚集。同样,腺苷增强了抑制程度。这些结果强调了在天然全血环境中测量血小板聚集对于检测双嘧达莫抑制作用的重要性,并提示了该药物的作用方式。

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