Structure of a homofructosan from Saussurea costus and anti-complementary activity of its sulfated derivatives

被引:33
作者
Fan, Hongwei [1 ,2 ]
Liu, Fei [1 ,2 ]
Bligh, S. W. Annie [3 ]
Shi, Songshan [1 ,2 ]
Wang, Shunchun [1 ,2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, MOE Key Lab Standardizat Chinese Med, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, SATCM Key Lab New Resources & Qual Evaluat Chines, Shanghai 201203, Peoples R China
[3] Univ Westminster, Fac Sci & Technol, Dept Complementary Med, London W1W 6UW, England
基金
中国国家自然科学基金;
关键词
Polysaccharide; Saussurea costus; Homofructosan; Sulfated derivatives; Anti-complement; HEPARIN-BINDING SITE; ANTICOAGULANT ACTIVITY; COMPLEMENT ACTIVATION; ANTICOMPLEMENTARY ACTIVITY; BIOLOGICAL-ACTIVITIES; POLYSACCHARIDE; FUCANS; SYSTEM; LAPPA; CHROMATOGRAPHY;
D O I
10.1016/j.carbpol.2014.01.084
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A homogeneous water-soluble polysaccharide APS-W1, (2 -> 1)-beta-D-fructofuranosan, with an average molecular weight of 3.9 kDa, was isolated and characterized from the roots of Saussurea costus. Five sulfated derivatives of APS-W1 with different degrees of sulfation were prepared and they showed strong inhibitory effect on the complement activation through the classical pathway (CP50: 2.2-18.9 mu g/mL; 8.3 mu g/mL for heparin) and alternative pathway (AP(50): 11.4-115.8 mu g/mL; 89.2 mu g/mL for heparin). Mechanism studies by using complement-depleted sera indicated that sulfated derivatives with different positions of sulfation targeted to different complement proteins. Meanwhile the sulfated derivatives have limited anticoagulant effect based on re-calcification time and thrombin time. These results suggested that the sulfated derivatives prepared from APS-W1 could be promising potential complement inhibitors for the treatment of diseases caused by an over-activated complement system. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:152 / 160
页数:9
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