血小板ADP受体拮抗剂氯吡格雷与AR-C69931MX对缺血性心脏病患者药效学作用的比较。

Comparison of the pharmacodynamic effects of the platelet ADP receptor antagonists clopidogrel and AR-C69931MX in patients with ischaemic heart disease.

作者信息

Storey Robert F, Wilcox Robert G, Heptinstall Stan

机构信息

Cardiovascular Medicine, University Hospital, Queen's Medical Centre, Nottingham, NG7 2UH, UK.

出版信息

Platelets. 2002 Nov;13(7):407-13. doi: 10.1080/0953710021000024402.

Abstract

We compared the antiplatelet effects of clopidogrel and the intravenous platelet P2Y(12) receptor antagonist AR-C69931MX, which acts on the same receptor as clopidogrel by a different and reversible mechanism and, unlike clopidogrel, is active in vitro. Thirteen patients with acute coronary syndromes entered into a phase II study of intravenous AR-C69931MX (Group 1) and eight patients undergoing intracoronary stent implantation and treated with clopidogrel (Group 2) were studied using a whole blood single-platelet counting aggregation assay. Group 2 patients were also studied using turbidimetry with ADP and TRAP as agonists and whole blood [(14)C]5HT release to study dense granule secretion in response to ADP, collagen and TRAP. In Group 2 studies, a therapeutic concentration of AR-C69931MX was added in vitro before and after clopidogrel administration. AR-C69931MX in Group 1 achieved greater inhibition of ADP-induced platelet aggregation than clopidogrel in Group 2 and AR-C69931MX in vitro added to the effects of clopidogrel on ADP-induced aggregation. AR-C69931MX but not clopidogrel inhibited TRAP-induced aggregation and granule secretion and AR-C69931MX had a more consistent inhibitory effect on collagen-induced responses. In conclusion, therapeutic administration of clopidogrel moderately inhibits platelet P2Y(12) receptor activation and substantially greater P2Y(12) receptor blockade can be achieved with AR-C69931MX.

摘要

我们比较了氯吡格雷与静脉内血小板P2Y(12)受体拮抗剂AR-C69931MX的抗血小板作用,AR-C69931MX通过不同的可逆机制作用于与氯吡格雷相同的受体,并且与氯吡格雷不同,它在体外具有活性。13例急性冠脉综合征患者进入静脉内AR-C69931MX的II期研究(第1组),8例接受冠状动脉内支架植入并接受氯吡格雷治疗的患者(第2组),使用全血单血小板计数聚集试验进行研究。第2组患者还使用比浊法,以ADP和TRAP作为激动剂,并通过全血[(14)C]5HT释放来研究对ADP、胶原和TRAP的反应中致密颗粒的分泌。在第2组研究中,在氯吡格雷给药前后在体外添加治疗浓度的AR-C69931MX。第1组中的AR-C69931MX对ADP诱导的血小板聚集的抑制作用比第2组中的氯吡格雷更强,并且AR-C69931MX在体外增强了氯吡格雷对ADP诱导聚集的作用。AR-C69931MX而非氯吡格雷抑制TRAP诱导的聚集和颗粒分泌,并且AR-C69931MX对胶原诱导的反应具有更一致的抑制作用。总之,氯吡格雷的治疗性给药适度抑制血小板P2Y(12)受体激活,而AR-C69931MX可实现更大程度的P2Y(12)受体阻断。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索