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南海海带多糖组分的抗血栓作用。

Antithrombotic effect of a polysaccharide fraction from Laminaria japonica from the South China Sea.

机构信息

Institute of Cardiovascular Diseases, First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China; Department of Physiology, Pre-Clinical Science, Guangxi Medical University, Nanning, 530021, China.

出版信息

Phytother Res. 2011 Sep;25(9):1362-6. doi: 10.1002/ptr.3433. Epub 2011 Feb 21.

Abstract

Some in vitro studies have identified an antithrombotic effect of polysaccharides from Laminaria japonica, but this activity remains to be confirmed in vivo. In this study a polysaccharide fraction termed PLG was extracted from L. japonica in the Beibu Gulf in Guangxi, China, and its antithrombotic effects explored in rat models of carotid and venous thrombosis. Its anticoagulation and antiplatelet properties were assessed by measuring the prothrombin time (PT), activated partial thromboplastin time (APTT) and ADP-induced platelet aggregation rate (Agg(max)). Its effects on bleeding time were measured using the tail transection method. It was found that pretreatment with an intraperitoneal injection of PLG at 2.5 or 5.0 mg/kg significantly prolonged the occlusion time in the carotid thrombosis model, and a dose of 5.0 mg/kg reduced the thrombus weight in the venous thrombosis model. Pretreatment with PLG (5.0 mg/kg) increased the APTT and decreased the ADP-induced platelet Agg(max). Neither dose of PLG significantly prolonged the bleeding time compared with the control group. In an in vitro anticoagulation assay using human plasma, PLG at 57.14, 28.57 and 28.57 μg/mL inhibited APTT and PT in a concentration-dependent manner. The results show that PLG possesses antithrombotic activity in a rat model, and that it may prove to be clinically useful in humans.

摘要

一些体外研究已经确定了来自日本昆布的多糖的抗血栓作用,但这种活性仍有待在体内得到证实。在这项研究中,从中国广西北部湾的海带中提取了一种多糖级分 PLG,并在颈动脉和静脉血栓形成的大鼠模型中探索了其抗血栓作用。通过测量凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)和 ADP 诱导的血小板聚集率(Agg(max))来评估其抗凝和抗血小板特性。使用尾切断法测量其对出血时间的影响。结果发现,腹腔内注射 2.5 或 5.0mg/kg 的 PLG 预处理可显著延长颈动脉血栓形成模型中的闭塞时间,而 5.0mg/kg 的剂量可降低静脉血栓形成模型中的血栓重量。PLG(5.0mg/kg)预处理可延长 APTT 并降低 ADP 诱导的血小板 Agg(max)。与对照组相比,两种剂量的 PLG 均未显著延长出血时间。在用人血浆进行的体外抗凝测定中,PLG 在 57.14、28.57 和 28.57μg/ml 浓度下以浓度依赖性方式抑制 APTT 和 PT。结果表明,PLG 在大鼠模型中具有抗血栓作用,并且在人类中可能具有临床应用价值。

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