Gershlick A H, Syndercombe-Court Y D, Murday A J, Lewis C T, Mills P G
Cardiovasc Res. 1984 Jul;18(7):391-6. doi: 10.1093/cvr/18.7.391.
We have shown previously that experimental autogenous vein grafts activate platelets for up to four months following operation. In the present study, animals were treated with middle dose ASA (10 mg X kg-1 X 24 h-1) plus dipyridamole (8 mg X kg-1 X 24 h-1) and followed for 8 months. Despite this treatment, platelets were activated by the vein graft for up to four months after operation but not after this time. Similarly, treatment with low dose ASA (0.5 mg X kg-1 X 24 h-1) plus dipyridamole (8 mg X kg-1 X 25 h-1), high dose ASA (40 mg X kg-1 X 24 h-1) plus dipyridamole (8 mg X kg-1 X 24 h-1), or dipyridamole alone (8 mg X kg-1 X 24 h-1), did not prevent the vein graft-induced activation of platelets. Full inhibition of platelet arachidonic acid metabolism was demonstrated in the high dose ASA plus dipyridamole group. These results suggest that the interaction between the vessel wall and platelet is not inhibited by ASA plus dipyridamole. Platelets have first to be activated before causing intimal hyperplasia. Since aspirin and dipyridamole did not prevent activation of platelets by the graft, this drug combination is unlikely to prevent the development of intimal hyperplasia in the graft wall.
我们之前已经表明,实验性自体静脉移植物在术后长达四个月的时间里都会激活血小板。在本研究中,动物接受中剂量阿司匹林(10毫克×千克⁻¹×24小时⁻¹)加双嘧达莫(8毫克×千克⁻¹×24小时⁻¹)治疗,并随访8个月。尽管进行了这种治疗,但静脉移植物在术后长达四个月的时间里仍会激活血小板,但在此之后则不会。同样,低剂量阿司匹林(0.5毫克×千克⁻¹×24小时⁻¹)加双嘧达莫(8毫克×千克⁻¹×25小时⁻¹)、高剂量阿司匹林(40毫克×千克⁻¹×24小时⁻¹)加双嘧达莫(8毫克×千克⁻¹×24小时⁻¹)或单独使用双嘧达莫(8毫克×千克⁻¹×24小时⁻¹)治疗,均不能防止静脉移植物诱导的血小板激活。高剂量阿司匹林加双嘧达莫组显示血小板花生四烯酸代谢受到完全抑制。这些结果表明,血管壁与血小板之间的相互作用不会被阿司匹林加双嘧达莫所抑制。血小板必须首先被激活,然后才会导致内膜增生。由于阿司匹林和双嘧达莫不能防止移植物激活血小板,这种药物组合不太可能防止移植物壁内膜增生的发展。