Suppr超能文献

香豆素衍生物AD6通过干扰凝血酶刺激的人血小板中的磷脂酶A2活性来抑制花生四烯酸的释放。

The coumarin derivative AD6 inhibits the release of arachidonic acid by interfering with phospholipase A2 activity in human platelets stimulated with thrombin.

作者信息

Porcellati S, Costantini V, Prosdocimi M, Stasi M, Pistolesi R, Nenci G G, Goracci G

机构信息

Dipartimento di Medicina Sperimentale e Scienze Biochimiche, Università di Perugia, Italy.

出版信息

Agents Actions. 1990 Mar;29(3-4):364-73. doi: 10.1007/BF01966469.

Abstract

AD6 is a coumarin derivative which is able to inhibit platelet aggregation and release due to various agonists as adrenaline, PAF, Ca++ ionophore and others. It has been demonstrated that this compound reduces the production of free arachidonate and diglyceride from human platelets pulse-labeled with radioactive arachidonic acid thus suggesting a possible interference with the activity of phospholipase A2 and/or phospholipase C. The present report indicates that the drug has no effect on the increase of the labeling of phosphatidic acid which takes place when platelets pulse-labeled with arachidonic acid are stimulated with thrombin. Furthermore, AD6 is not able to cause changes on the metabolism of phosphoinositides monitored using platelets pre-labeled with [3H] inositol. These observations exclude the possibility that AD6 interferes with phospholipase C activity. Experiments with platelets pulse-labeled with arachidonate suggest that AD6 inhibits phospholipase(s) A2 activity or modulate negatively one or more processes involved in its activation.

摘要

AD6是一种香豆素衍生物,它能够抑制由多种激动剂(如肾上腺素、血小板活化因子、钙离子载体等)引起的血小板聚集和释放。已经证明,该化合物可减少用放射性花生四烯酸脉冲标记的人血小板中游离花生四烯酸和甘油二酯的产生,因此提示其可能干扰磷脂酶A2和/或磷脂酶C的活性。本报告指出,当用凝血酶刺激用花生四烯酸脉冲标记的血小板时,该药物对磷脂酸标记的增加没有影响。此外,AD6不能引起在用[3H]肌醇预标记的血小板中监测到的磷酸肌醇代谢的变化。这些观察结果排除了AD6干扰磷脂酶C活性的可能性。用花生四烯酸脉冲标记血小板的实验表明,AD6抑制磷脂酶A2的活性或对其激活过程中涉及的一个或多个过程产生负调节作用。

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