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首页> 外文期刊>Platelets >Inhibitory effects of Terminalia arjuna on platelet activation in vitro in healthy subjects and patients with coronary artery disease.
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Inhibitory effects of Terminalia arjuna on platelet activation in vitro in healthy subjects and patients with coronary artery disease.

机译:榄仁对健康受试者和冠心病患者体外血小板活化的抑制作用。

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摘要

Terminalia arjuna (TA) is a medicinal plant used as a cardiotonic in ayurveda. Besides others, scientific evidence dictates its strong hypolipidemic and antioxidant properties. However, anti-inflammatory and antiplatelet aggregatory properties of TA are not known. The present study demonstrates in vitro effects of its ethanolic bark extract (TAE) on platelet function indices. Twenty patients of angiographically proven coronary artery disease (CAD) were included in Group I and 20 age and sex-matched controls were included in Group II. Platelet activation was monitored by determining P-selectin (CD62P) expression, intracellular free calcium (Ca(2+)) release and platelet aggregation. In vitro effect of TA on platelets function indices was determined by incubating the platelets with TAE in a time and dose-dependent manner in presence/absence of ADP. TAE was able to significantly inhibit platelet aggregation both in patient and control groups. Significant attenuation in Ca(2+) release and expression of CD62P was also observed with TAE. Our data clearly demonstrates that the bark extract of TA decreases platelet activation and may possess antithrombotic properties. The possible mechanism of action could be by desensitizing platelets to the agonist by competing with platelet receptor or by interfering with signal transduction. Thus, TA can be exploited for its therapeutic potential in CAD and related cardiovascular disorders.
机译:Terminalia arjuna(TA)是在阿育吠陀中用作强心剂的药用植物。除其他外,科学证据表明其具有强大的降血脂和抗氧化特性。然而,TA的抗炎和抗血小板聚集特性是未知的。本研究证明了其乙醇树皮提取物(TAE)对血小板功能指标的体外作用。第一组包括20例经血管造影证实的冠状动脉疾病(CAD)患者,第二组包括20个年龄和性别匹配的对照。通过测定P-选择蛋白(CD62P)表达,细胞内游离钙(Ca(2+))释放和血小板聚集来监测血小板活化。通过在存在/不存在ADP的情况下以时间和剂量依赖性方式将血小板与TAE一起温育来测定TA对血小板功能指数的体外作用。 TAE能够显着抑制患者和对照组的血小板聚集。 TAE还观察到Ca(2+)释放和CD62P表达的显着衰减。我们的数据清楚地表明,TA的树皮提取物可降低血小板活化,并可能具有抗血栓形成特性。可能的作用机制可能是通过与血小板受体竞争或干扰信号转导使血小板对激动剂不敏感。因此,可以利用TA在CAD和相关心血管疾病中的治疗潜力。

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