Oetliker O, Lüthy C, Siegrist M, Odavic R
Arzneimittelforschung. 1987 May;37(5):566-8.
The effect of varied doses of dipyridamole (Persantin) on the arachidonic acid metabolites prostaglandin (PG)I2, PGE2 and thromboxane (TX)A2 has been studied in human skin fibroblasts cultured in vitro. A 24-h exposure to the drug induced a dose-dependent increase of all the examined prostaglandins (PG's). Bradykinin stimulation of cells that had been preexposed to the drug induced a continuous increase in PG-production as compared to controls, despite the absence of the drug. In addition, an acute 5-min exposure to dipyridamole produced an increased thromboxane production, but no consistent changes of PGI2 or PGE2, and it inhibited significantly and dose-dependently the comcomitant bradykinin stimulated production of all the examined PG's. The implications of a combined dipyridamole-acetylsalicylic acid therapy is discussed.
在体外培养的人皮肤成纤维细胞中,研究了不同剂量双嘧达莫(潘生丁)对花生四烯酸代谢产物前列腺素(PG)I2、PGE2和血栓素(TX)A2的影响。药物暴露24小时导致所有检测的前列腺素(PG)呈剂量依赖性增加。与对照组相比,对预先暴露于该药物的细胞进行缓激肽刺激会导致PG生成持续增加,尽管此时不存在该药物。此外,双嘧达莫急性暴露5分钟会使血栓素生成增加,但PGI2或PGE2没有一致变化,并且它显著且剂量依赖性地抑制了缓激肽同时刺激的所有检测PG的生成。讨论了双嘧达莫 - 乙酰水杨酸联合治疗的意义。