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从挪威海螯虾(Nephrops norvegicus)壳中分离出的硫酸化糖胺聚糖的抗凝特性和对 HCT116 人结肠细胞系的细胞毒性作用。

Anticoagulant properties and cytotoxic effect against HCT116 human colon cell line of sulfated glycosaminoglycans isolated from the Norway lobster (Nephrops norvegicus) shell.

机构信息

Unité Enzymes et Bioconversion, Ecole Nationale d'Ingénieurs de Sfax, University of Sfax, Km 4 Road Soukra, 3038 Sfax, Tunisia.

Laboratoire de Génétique, Biodiversité et Valorisation des Bioressources (LR 11-ES 41), University of Monastir, Tunisia.

出版信息

Biomed Pharmacother. 2016 May;80:322-330. doi: 10.1016/j.biopha.2016.03.027. Epub 2016 Apr 6.

Abstract

Sulfated glycosaminoglycans (SGNL) were extracted for the first time from Norway lobster (Nephrops norvegicus) shell. The monosaccharide composition analysed by GC/MS revealed the presence of galacturonic acid, glucuronic acid, N-acetylgalactosamine and N-acetylglucosamine. The analysis of SGNL with acetate cellulose electrophoresis in Zn-acetate revealed the presence of heparan sulfate (HS) and dermatan sulfate (DS). SGNL were evaluated for their anticoagulant activities using activated partial thromboplastin time (aPTT), thrombin time (TT) and prothrombine time (PT) tests. After 21h incubation, HCT116 cell proliferation was inhibited (p<0.05) between 39.7 and 54.8% at 1.5-7.5mg/mL of SGNL. SGNL don't show hemolytic activity towards bovine erythrocytes and no cytotoxicity against the normal lymphocytes. The antiproliferative efficacy of these lobster glycosaminoglycans were probably related with the higher sulfate content. SGNL demonstrated promising antiproliferative and anticoagulant potential, which may be used as a novel, effective and promising antithrombotic agent.

摘要

硫酸化糖胺聚糖(SGNL)首次从挪威海螯虾(Nephrops norvegicus)壳中提取。通过 GC/MS 分析的单糖组成表明存在半乳糖醛酸、葡萄糖醛酸、N-乙酰半乳糖胺和 N-乙酰葡萄糖胺。用 Zn-乙酸盐中的醋酸纤维素电泳分析 SGNL 显示存在肝素硫酸盐(HS)和硫酸皮肤素(DS)。使用活化部分凝血活酶时间(aPTT)、凝血酶时间(TT)和凝血酶原时间(PT)试验评估 SGNL 的抗凝活性。孵育 21 小时后,在 1.5-7.5mg/mL 的 SGNL 下,HCT116 细胞增殖抑制率为 39.7%至 54.8%(p<0.05)。SGNL 对牛红细胞没有溶血活性,对正常淋巴细胞也没有细胞毒性。这些龙虾糖胺聚糖的抗增殖功效可能与较高的硫酸盐含量有关。SGNL 表现出有前景的抗增殖和抗凝潜力,可作为一种新型、有效和有前途的抗血栓形成剂。

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