Jakob W, Zipper J, Sávoly S B, Siems W E, Jentzsch K D
Exp Pathol. 1982;22(4):217-24. doi: 10.1016/s0232-1513(82)80011-x.
Dipyridamole, a potent inhibitor of the nucleoside transport into cells, has recently been reported to stimulate the proliferation of capillary endothelial cells in the heart and skeletal muscle of rats following long-term treatment. We tested this drug on cultured calf aortic endothelial cells and obtained no evidence that dipyridamole is able to stimulate directly the proliferation and migration of these cells. By using the chorioallantoic membrane model we observed that the pharmaceutical preparation Curantyl induces vascular responses almost regularly. This effect, however, was found to be dependent on the high concentration of hydrogen ions in this preparation and could be prevented by increasing the pH value. A direct angiogenic effect of dipyridamole could not be demonstrated on the CAM.
双嘧达莫是一种有效的核苷转运至细胞的抑制剂,最近有报道称,长期治疗后,它能刺激大鼠心脏和骨骼肌中的毛细血管内皮细胞增殖。我们在培养的小牛主动脉内皮细胞上测试了这种药物,没有发现证据表明双嘧达莫能够直接刺激这些细胞的增殖和迁移。通过使用绒毛尿囊膜模型,我们观察到药物制剂Curantyl几乎总能诱导血管反应。然而,发现这种效应取决于该制剂中高浓度的氢离子,并且可以通过提高pH值来预防。在绒毛尿囊膜上未证实双嘧达莫有直接的血管生成作用。