Suppr超能文献

血栓素A2类似物(U-46619)刺激血管前列环素2的合成。

Thromboxane A2 analogue (U-46619) stimulates vascular PGI2 synthesis.

作者信息

Jeremy J Y, Mikhailidis D P, Dandona P

出版信息

Eur J Pharmacol. 1985 Jan 2;107(2):259-62. doi: 10.1016/0014-2999(85)90066-4.

Abstract

Since platelet release reaction products (e.g. serotonin, ADP) stimulate prostacyclin (PGI2) release in vitro, we have investigated whether thromboxane A2 (TXA2) also has a similar effect. An analogue, U-46619, was used for the experiments, since TXA2 is extremely unstable. U-46619 stimulated rat aortic PGI2 release; this stimulation was abolished by (a) EDTA and (b) verapamil. We conclude that TXA2 is a calcium-dependent stimulator of PGI2 release; this property may be relevant to the limitation of platelet aggregates in vivo and to vascular injury.

摘要

由于血小板释放反应产物(如5-羟色胺、二磷酸腺苷)在体外能刺激前列环素(PGI2)释放,我们研究了血栓素A2(TXA2)是否也有类似作用。由于TXA2极不稳定,实验中使用了其类似物U-46619。U-46619刺激大鼠主动脉释放PGI2;这种刺激可被(a)乙二胺四乙酸(EDTA)和(b)维拉帕米消除。我们得出结论,TXA2是PGI2释放的钙依赖性刺激物;这一特性可能与体内血小板聚集体的限制及血管损伤有关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验