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杨梅素是叶片中的主要黄酮类化合物,是血小板硫醇异构酶PDI和ERp5的新型抑制剂。

Myricetin, the Main Flavonoid in Leaf, Is a Novel Inhibitor of Platelet Thiol Isomerases PDI and ERp5.

作者信息

Gaspar Renato Simões, da Silva Samira Abdalla, Stapleton Jennifer, Fontelles João Lucas de Lima, Sousa Hiran Reis, Chagas Vinicyus Teles, Alsufyani Shuruq, Trostchansky Andrés, Gibbins Jonathan M, Paes Antonio Marcus de Andrade

机构信息

Institute for Cardiovascular and Metabolic Research, School of Biological Sciences, University of Reading, Reading, United Kingdom.

Laboratory of Experimental Physiology, Department of Physiological Sciences, Federal University of Maranhão, São Luís, Brazil.

出版信息

Front Pharmacol. 2020 Jan 31;10:1678. doi: 10.3389/fphar.2019.01678. eCollection 2019.

Abstract

BACKGROUND

Flavonoids have been characterized as a prominent class of compounds to treat thrombotic diseases through the inhibition of thiol isomerases. is a flavonoid-rich medicinal plant that contains myricetin and gallic acid. Little is known about the potential antiplatelet properties of and its constituent flavonoids.

OBJECTIVE

To evaluate the antiplatelet effects and mechanism of action of a polyphenol-rich extract (PESc) from leaf and its most prevalent polyphenols, myricetin and gallic acid.

METHODS

PESc, myricetin, and gallic acid were incubated with platelet-rich plasma and washed platelets to assess platelet aggregation and activation. platelet adhesion and thrombus formation as well as bleeding time were performed. Finally, myricetin was incubated with recombinant thiol isomerases to assess its potential to bind and inhibit these, while molecular docking studies predicted possible binding sites.

RESULTS

PESc decreased platelet activation and aggregation induced by different agonists. Myricetin exerted potent antiplatelet effects, whereas gallic acid did not. Myricetin reduced the ability of platelets to spread on collagen, form thrombi without affecting hemostasis . Fluorescence quenching studies suggested myricetin binds to different thiol isomerases with similar affinity, despite inhibiting only protein disulfide isomerase (PDI) and ERp5 reductase activities. Finally, molecular docking studies suggested myricetin formed non-covalent bonds with PDI and ERp5.

CONCLUSIONS

PESc and its most abundant flavonoid myricetin strongly inhibit platelet function. Additionally, myricetin is a novel inhibitor of ERp5 and PDI, unveiling a new therapeutic perspective for the treatment of thrombotic disorders.

摘要

背景

黄酮类化合物被认为是一类通过抑制硫醇异构酶来治疗血栓性疾病的重要化合物。[植物名称]是一种富含黄酮类化合物的药用植物,含有杨梅素和没食子酸。关于[植物名称]及其所含黄酮类化合物的潜在抗血小板特性知之甚少。

目的

评估[植物名称]叶中富含多酚的提取物(PESc)及其最主要的多酚类物质杨梅素和没食子酸的抗血小板作用及作用机制。

方法

将PESc、杨梅素和没食子酸与富血小板血浆和洗涤后的血小板一起孵育,以评估血小板聚集和活化情况。进行体内血小板黏附、血栓形成以及出血时间测定。最后,将杨梅素与重组硫醇异构酶孵育,以评估其结合和抑制这些酶的潜力,同时分子对接研究预测可能的结合位点。

结果

PESc可降低不同激动剂诱导的血小板活化和聚集。杨梅素具有强大的抗血小板作用,而没食子酸则没有。杨梅素降低了血小板在胶原蛋白上铺展、形成血栓的能力,且不影响止血功能。荧光猝灭研究表明,尽管杨梅素仅抑制蛋白二硫键异构酶(PDI)和ERp5还原酶活性,但它以相似的亲和力与不同的硫醇异构酶结合。最后,分子对接研究表明杨梅素与PDI和ERp5形成非共价键。

结论

PESc及其含量最丰富的黄酮类化合物杨梅素强烈抑制血小板功能。此外,杨梅素是一种新型的ERp5和PDI抑制剂,为血栓性疾病的治疗开辟了新的治疗前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e56f/7011086/2f558a5d4faf/fphar-10-01678-g001.jpg

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