Suppr超能文献

瑞舒伐他汀对人血小板聚集的抑制作用。

The Anti-Aggregative Potential of Resolvin E1 on Human Platelets.

机构信息

Department of Haemostasis and Haemostatic Disorders, Chair of Biomedical Sciences, Medical University of Lodz, Mazowiecka 6/8, 92-215 Lodz, Poland.

Department of General Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland.

出版信息

Molecules. 2023 Jul 11;28(14):5323. doi: 10.3390/molecules28145323.

Abstract

Resolvin E1 is a metabolite of eicosapentaenoic acid (EPA) which is one of the omega-3 polyunsaturated fatty acids (omega-3 PUFAs). The antiplatelet properties of omega-3 PUFAs are well known, but the effect of resolvin E1 on platelets via the collagen receptors is extremely poorly reported. We investigated the effect of resolvin E1 on collagen-induced platelet aggregation, activation, and reactivity, and also platelet membrane fluidity. The ultimate and statistically significant results showed that resolvin E1 may inhibit platelet reactivity due to the reduction of collagen-induced platelet aggregation in platelet-rich plasma and isolated platelets, but not in whole blood. Also, resolvin E1 significantly reduced P-selectin exposure on collagen-stimulated platelets. Moreover, we demonstrated that resolvin E1 can maintain platelet membrane structure (without increasing membrane fluidity). The association between platelet reactivity and membrane fluidity, including resolvin E1 and collagen receptors requires further research. However, the goal of this study was to shed light on the molecular mechanisms behind the anti-aggregative effects of resolvin E1 on platelets, which are still not fully clarified. We also indicate an innovative research direction focused on further analysis and then use of omega-3 PUFAs metabolites as antiplatelet compounds for future applications in the treatment and prevention of cardiovascular diseases.

摘要

解析 E1 是二十碳五烯酸(EPA)的一种代谢物,EPA 是一种ω-3 多不饱和脂肪酸(ω-3 PUFAs)。ω-3 PUFAs 的抗血小板特性是众所周知的,但解析 E1 通过胶原蛋白受体对血小板的作用却鲜有报道。我们研究了解析 E1 对胶原蛋白诱导的血小板聚集、激活和反应性以及血小板膜流动性的影响。最终的统计结果表明,解析 E1 可能通过减少富血小板血浆和分离血小板中胶原蛋白诱导的血小板聚集来抑制血小板反应性,但在全血中则没有。此外,解析 E1 还显著降低了胶原蛋白刺激的血小板上 P-选择素的暴露。此外,我们还证明,解析 E1 可以维持血小板膜结构(而不会增加膜流动性)。血小板反应性与膜流动性之间的关系,包括解析 E1 和胶原蛋白受体,需要进一步研究。然而,本研究的目的是阐明解析 E1 对血小板的抗聚集作用背后的分子机制,这些机制仍未完全阐明。我们还指出了一个创新的研究方向,重点是进一步分析,然后将 ω-3 PUFAs 代谢物用作未来治疗和预防心血管疾病的抗血小板化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65ca/10385542/598ed775a1e9/molecules-28-05323-g001.jpg

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