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从绿藻单枝藻中分离得到的一种硫酸多糖的结构与抗凝性质。

Structure and anticoagulant property of a sulfated polysaccharide isolated from the green seaweed Monostroma angicava.

机构信息

Key Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China; Department of Food and Biochemical Engineering, Yantai Vocational College, Yantai 264670, China.

Key Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.

出版信息

Carbohydr Polym. 2017 Mar 1;159:195-206. doi: 10.1016/j.carbpol.2016.12.013. Epub 2016 Dec 6.

DOI:10.1016/j.carbpol.2016.12.013
PMID:28038749
Abstract

An anticoagulant-active polysaccharide PF2 was extracted with boiling water from the green seaweed Monostroma angicava, further purified by anion-exchange and size-exclusion chromatography. PF2 was a rhamnan-type sulfated polysaccharide with molecular weight of about 88.1kDa. Results of chemical and spectroscopic analyses demonstrated that PF2 consisted of→3)-α-l-Rhap-(1→ and →2)-α-l-Rhap-(1→residues, with partially branches at C-2 of→3)-α-l-Rhap-(1→residues. Sulfate groups were substituted at C-3 of →2)-α-l-Rhap-(1→ residues. The sulfated polysaccharide PF2 had a high anticoagulant action, and the mechanism of anticoagulant activity mediated by PF2 was mainly attributed to strong potentiation thrombin by heparin cofactor II. PF2 also exhibited weak effect on antithrombin-dependent thrombin or factor Xa inhibition. The fibrin(ogen)olytic activity and thrombolytic activity of PF2 were also evaluated. The investigation revealed that PF2 was a novel sulfated rhamnan differing from previously described sulfated polysaccharides from green seaweed and could be a potential anticoagulant polysaccharide.

摘要

从绿藻单枝马尾藻中用沸水提取具有抗凝活性的多糖 PF2,并用阴离子交换和分子筛层析进一步纯化。PF2 是一种鼠李半乳聚糖型硫酸多糖,分子量约为 88.1kDa。化学和光谱分析结果表明,PF2 由→3)-α-l-Rhap-(1→和→2)-α-l-Rhap-(1→残基组成,→3)-α-l-Rhap-(1→残基在 C-2 处部分分支。硫酸基团取代了→2)-α-l-Rhap-(1→残基的 C-3。硫酸多糖 PF2 具有很强的抗凝作用,其抗凝活性的机制主要归因于肝素辅因子 II 对凝血酶的强烈增强作用。PF2 对依赖抗凝血酶的凝血酶或因子 Xa 的抑制作用也较弱。还评估了 PF2 的纤维蛋白(原)溶解活性和溶栓活性。研究表明,PF2 是一种新型的硫酸鼠李聚糖,与先前描述的绿藻硫酸多糖不同,可能是一种有潜力的抗凝多糖。

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