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褐藻多酚 Eckol 和 Dieckol 的抗血栓和纤维蛋白溶解活性。

Antithrombotic and profibrinolytic activities of eckol and dieckol.

机构信息

Department of Herbal Medicinal Pharmacology, College of Herbal Bio-Industry, Daegu Haany University, Republic of Korea.

出版信息

J Cell Biochem. 2012 Sep;113(9):2877-83. doi: 10.1002/jcb.24163.

Abstract

In order to develop new anticoagulant agents, two single compounds (eckol and dieckol) were isolated from Eisenia bicyclis and examined their anticoagulant activities by monitoring activated partial thromboplastin time (aPTT), prothrombin time (PT) as well as cell-based thrombin and activated factor X (FXa) generation activities. And the effects of eckol and dieckol on the expression of plasminogen activator inhibitor type 1 (PAI-1) and tissue-type plasminogen activator (t-PA) were tested in tumor necrosis factor-α (TNF-α) activated human umbilical vein endothelial cells (HUVECs). Data showed that eckol and dieckol prolonged aPTT and PT significantly and inhibited thrombin and FXa activities. They also inhibited the generation of thrombin or FXa in HUVECs. In accordance with these anticoagulant activities, eckol or dieckol showed anticoagulant effect in vivo. Furthermore, eckol and dieckol inhibited TNF-α induced PAI-1 production and the ratio between PAI-1 and t-PA was found to be significantly decreased by eckol and dieckol. Surprisingly, these anticoagulant and profibrinolytic effects of dieckol were better than those of eckol indicating that hydroxyl group in eckol positively regulated anticoagulant function of eckol. Therefore, these results suggest that eckol or dieckol possesses antithrombotic activities and provides a possibility to develop as an agent for the anticoagulation.

摘要

为了开发新型抗凝剂,从双齿围沙蚕中分离得到两种单体化合物(褐藻多酚和二羟基褐藻多酚),通过监测活化部分凝血活酶时间(aPTT)、凝血酶原时间(PT)以及基于细胞的凝血酶和活化因子 X(FXa)生成活性来研究其抗凝活性。并在肿瘤坏死因子-α(TNF-α)激活的人脐静脉内皮细胞(HUVEC)中测试褐藻多酚和二羟基褐藻多酚对纤溶酶原激活物抑制剂 1(PAI-1)和组织型纤溶酶原激活物(t-PA)表达的影响。结果表明,褐藻多酚和二羟基褐藻多酚显著延长 aPTT 和 PT,抑制凝血酶和 FXa 活性。它们还抑制 HUVECs 中凝血酶或 FXa 的生成。根据这些抗凝活性,褐藻多酚或二羟基褐藻多酚在体内表现出抗凝作用。此外,褐藻多酚和二羟基褐藻多酚抑制 TNF-α诱导的 PAI-1 产生,并且发现褐藻多酚和二羟基褐藻多酚显著降低了 PAI-1 与 t-PA 的比值。令人惊讶的是,二羟基褐藻多酚的这些抗凝和纤维蛋白溶解作用优于褐藻多酚,表明褐藻多酚中的羟基基团正向调节褐藻多酚的抗凝功能。因此,这些结果表明褐藻多酚或二羟基褐藻多酚具有抗血栓形成活性,并为开发抗凝剂提供了可能性。

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