Suppr超能文献

姜黄素通过激活腺苷 A 受体刺激蛋白激酶 A 并增强坎格雷洛对血小板的抑制作用。

Curcumin by activation of adenosine A receptor stimulates protein kinase a and potentiates inhibitory effect of cangrelor on platelets.

机构信息

Sechenov Institute of Evolutionary Physiology and Biochemistry of the Russian Academy of Sciences, Thorez Prospect 44, Saint Petersburg, 194223, Russia.

Saint Petersburg State Chemical Pharmaceutical University, Professora Popova Street 14, Saint Petersburg, 197376, Russia.

出版信息

Biochem Biophys Res Commun. 2022 Jan 1;586:20-26. doi: 10.1016/j.bbrc.2021.11.006. Epub 2021 Nov 4.

Abstract

Curcumin is a natural polyphenol derived from the turmeric plant (Curcuma longa) which exhibits numerous beneficial effects on different cell types. Inhibition of platelet activation by curcumin is well known, however molecular mechanisms of its action on platelets are not fully defined. In this study, we used laser diffraction method for analysis of platelet aggregation and Western blot for analysis of intracellular signaling mechanisms of curcumin effects on platelets. We identified two new molecular mechanisms involved in the inhibitory effects of curcumin on platelet activation. Firstly, curcumin by activation of adenosine A receptor stimulated protein kinase A activation and phosphorylation of Vasodilator-stimulated phosphoprotein. Secondly, we demonstrated that curcumin even at low doses, which did not inhibit platelet aggregation, potentiated inhibitory effect of ADP receptor P2Y antagonist cangrelor which partly could be explained by activation of adenosine A receptor.

摘要

姜黄素是一种天然多酚类物质,来源于姜黄植物(Curcuma longa),对不同类型的细胞具有多种有益作用。姜黄素抑制血小板活化的作用已广为人知,但其对血小板作用的分子机制尚未完全确定。在这项研究中,我们使用激光衍射法分析血小板聚集,并用 Western blot 分析姜黄素对血小板的细胞内信号转导机制。我们确定了两种新的分子机制,涉及姜黄素抑制血小板活化的作用。首先,姜黄素通过激活腺苷 A 受体刺激蛋白激酶 A 的激活和血管扩张刺激磷蛋白的磷酸化。其次,我们证明,即使在低剂量下,姜黄素不会抑制血小板聚集,也可以增强 ADP 受体 P2Y 拮抗剂坎格雷洛的抑制作用,这部分可以通过激活腺苷 A 受体来解释。

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