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富含人参皂苷Rg3的红参提取物可抑制血小板活化和血栓形成。

Ginsenoside Rg3-enriched red ginseng extract inhibits platelet activation and thrombus formation.

作者信息

Jeong Dahye, Irfan Muhammad, Kim Sung-Dae, Kim Suk, Oh Jun-Hwan, Park Chae-Kyu, Kim Hyun-Kyoung, Rhee Man Hee

机构信息

Department of Veterinary Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu, Republic of Korea.

Research Center, Dongnam Institute of Radiological and Medical Sciences, Busan, Republic of Korea.

出版信息

J Ginseng Res. 2017 Oct;41(4):548-555. doi: 10.1016/j.jgr.2016.11.003. Epub 2017 Jan 13.

Abstract

BACKGROUND

Korean Red Ginseng has been used for several decades to treat many diseases, enhancing both immunity and physical strength. Previous studies have documented the therapeutic effects of ginseng, including its anticancer, antiaging, and anti-inflammatory activities. These activities are mediated by ginsenosides present in the ginseng plant. Ginsenoside Rg3, an effective compound from red ginseng, has been shown to have antiplatelet activity in addition to its anticancer and anti-inflammatory activities. Platelets are important for both primary hemostasis and the repair of the vessels after injury; however, they also play a crucial role in the development of acute coronary diseases. We prepared ginsenoside Rg3-enriched red ginseng extract (Rg3-RGE) to examine its role in platelet physiology.

METHODS

To examine the effect of Rg3-RGE on platelet activation , platelet aggregation, granule secretion, intracellular calcium ([Ca]) mobilization, flow cytometry, and immunoblot analysis were carried out using rat platelets. To examine the effect of Rg3-RGE on platelet activation , a collagen plus epinephrine-induced acute pulmonary thromboembolism mouse model was used.

RESULTS

We found that Rg3-RGE significantly inhibited collagen-induced platelet aggregation and [Ca] mobilization in a dose-dependent manner in addition to reducing ATP release from collagen-stimulated platelets. Furthermore, using immunoblot analysis, we found that Rg3-RGE markedly suppressed mitogen-activated protein kinase phosphorylation (i.e., extracellular stimuli-responsive kinase, Jun N-terminal kinase, p38) as well as the PI3K (phosphatidylinositol 3 kinase)/Akt pathway. Moreover, Rg3-RGE effectively reduced collagen plus epinephrine-induced mortality in mice.

CONCLUSION

These data suggest that ginsenoside Rg3-RGE could be potentially be used as an antiplatelet therapeutic agent against platelet-mediated cardiovascular disorders.

摘要

背景

韩国红参已被用于治疗多种疾病数十年,可增强免疫力和体力。先前的研究记录了人参的治疗作用,包括其抗癌、抗衰老和抗炎活性。这些活性由人参植物中存在的人参皂苷介导。人参皂苷Rg3是红参中的一种有效化合物,除了具有抗癌和抗炎活性外,还具有抗血小板活性。血小板对于初级止血和损伤后血管的修复都很重要;然而,它们在急性冠状动脉疾病的发展中也起着关键作用。我们制备了富含人参皂苷Rg3的红参提取物(Rg3-RGE),以研究其在血小板生理中的作用。

方法

为了研究Rg3-RGE对血小板活化的影响,使用大鼠血小板进行血小板聚集、颗粒分泌、细胞内钙([Ca])动员、流式细胞术和免疫印迹分析。为了研究Rg3-RGE对血小板活化的影响,使用胶原加肾上腺素诱导的急性肺血栓栓塞小鼠模型。

结果

我们发现,Rg3-RGE除了减少胶原刺激的血小板释放ATP外,还以剂量依赖的方式显著抑制胶原诱导的血小板聚集和[Ca]动员。此外,通过免疫印迹分析,我们发现Rg3-RGE显著抑制丝裂原活化蛋白激酶磷酸化(即细胞外刺激反应激酶、Jun N末端激酶、p38)以及PI3K(磷脂酰肌醇3激酶)/Akt途径。此外,Rg3-RGE有效降低了小鼠胶原加肾上腺素诱导的死亡率。

结论

这些数据表明,人参皂苷Rg3-RGE可能潜在地用作抗血小板治疗剂,用于治疗血小板介导的心血管疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f561/5628340/85899a42d330/gr1.jpg

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