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一种新型结构的岩藻糖型硫酸多糖来自 angicava Kjellm (绿藻门)及其生物活性。

A rhamnan-type sulfated polysaccharide with novel structure from Monostroma angicava Kjellm (Chlorophyta) and its bioactivity.

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.

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 Oct 1;173:732-748. doi: 10.1016/j.carbpol.2017.06.031. Epub 2017 Jun 12.

Abstract

A homogeneous polysaccharide was obtained from Monostroma angicava Kjellm by water extraction, preparative anion-exchange and size-exclusion chromatography. Results of chemical and spectroscopic analyses showed that the polysaccharide was a glucuronic acid-containing rhamnan-type sulfated polysaccharide. The backbone mainly consisted of →3)-α-l-Rhap-(1→ and →2)-α-l-Rhap-(1→ residues, partially sulfated at C-2 of →3)-α-l-Rhap-(1→ and C-3/C-4 of →2)-α-l-Rhap-(1→. The branching contained unsulfated or monosulfated 3-linked, 2-linked, 4-linked α-l-rhamnose and terminal β-d-glucuronic acid residues. The polysaccharide had strong antidiabetic activity assessed by glucose consumption, total cholesterol and triglyceride levels using human hepatocellular carcinoma (HepG2) and insulin-resistant HepG2 cells. The polysaccharide exhibited high anticoagulant property by activated partial thromboplastin time and thrombin time assays, and possessed high fibrin(ogen)olytic activity evaluated by plasminogen activator inhibitior-1, fibrin(ogen) degradation products and D-dimer levels using rats plasma. The investigation demonstrated that the polysaccharide from Monostroma angicava Kjellm was a novel sulfated rhamnan and could be a potential antidiabetic and anticoagulant polysaccharide.

摘要

从皱瘤海鞘(Monostroma angicava Kjellm)中提取的均一多糖,经过水提、制备性阴离子交换和凝胶过滤色谱分离纯化。化学和光谱分析结果表明,该多糖是一种含有葡萄糖醛酸的鼠李半乳聚糖型硫酸化多糖。其主链主要由→3)-α-l-Rhap-(1→和→2)-α-l-Rhap-(1→残基组成,部分在→3)-α-l-Rhap-(1→的 C-2 和→2)-α-l-Rhap-(1→的 C-3/C-4 位硫酸化。支链含有未硫酸化或单硫酸化的 3-连接、2-连接、4-连接的α-l-鼠李糖和末端β-d-葡萄糖醛酸残基。该多糖在人肝癌细胞(HepG2)和胰岛素抵抗 HepG2 细胞中通过葡萄糖消耗、总胆固醇和甘油三酯水平评估具有很强的抗糖尿病活性。该多糖通过活化部分凝血活酶时间和凝血酶时间测定显示出很强的抗凝活性,并通过纤溶酶原激活物抑制剂-1、纤维蛋白(原)降解产物和大鼠血浆中二聚体 D 水平评估显示出很强的纤维蛋白(原)溶解活性。研究表明,皱瘤海鞘(Monostroma angicava Kjellm)多糖是一种新型硫酸化鼠李聚糖,可能是一种有潜力的抗糖尿病和抗凝多糖。

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