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三种藻类硫酸化多糖的结构特征、免疫调节及抗禽流感病毒活性的表征与比较

Characterization and Comparison of the Structural Features, Immune-Modulatory and Anti-Avian Influenza Virus Activities Conferred by Three Algal Sulfated Polysaccharides.

作者信息

Song Lin, Chen Xiaolin, Liu Xiaodong, Zhang Fubo, Hu Linfeng, Yue Yang, Li Kecheng, Li Pengcheng

机构信息

Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, No.7 Nanhai Road, Qingdao 266071, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Mar Drugs. 2015 Dec 29;14(1):4. doi: 10.3390/md14010004.

Abstract

Three marine macroalgae, i.e., Grateloupia filicina, Ulva pertusa and Sargassum qingdaoense, were selected as the deputies of Rhodophyta, Chlorophyta and Ochrophyta for comparative analysis of the molecular structures and biological activities of sulfated polysaccharides (SP). The ratio of water-soluble polysaccharides, the monosaccharide composition and the sulfated contents of three extracted SPs were determined, and their structures were characterized by Fourier transformation infrared spectroscopy. In addition, biological activity analysis showed that all three SPs had immune-modulatory activity both in vitro and in vivo, and SPs from S. qingdaoense had the best effect. Further bioassays showed that three SPs could not only enhance the immunity level stimulated by inactivated avian influenza virus (AIV) in vivo but also significantly inhibited the activity of activated AIV (H9N2 subtype) in vitro. G. filicina SP exhibited the strongest anti-AIV activity. These results revealed the variations in structural features and bioactivities among three SPs and indicated the potential adjuvants for immune-enhancement and anti-AIV.

摘要

选取三种海洋大型藻类,即蜈蚣藻、孔石莼和青岛马尾藻,分别作为红藻门、绿藻门和褐藻门的代表,对其硫酸化多糖(SP)的分子结构和生物活性进行比较分析。测定了三种提取的SP的水溶性多糖比例、单糖组成和硫酸化含量,并通过傅里叶变换红外光谱对其结构进行了表征。此外,生物活性分析表明,三种SP在体外和体内均具有免疫调节活性,其中青岛马尾藻的SP效果最佳。进一步的生物测定表明,三种SP不仅能提高体内灭活禽流感病毒(AIV)刺激的免疫水平,还能在体外显著抑制活化的AIV(H9N2亚型)的活性。蜈蚣藻SP表现出最强的抗AIV活性。这些结果揭示了三种SP在结构特征和生物活性方面的差异,并表明了其作为免疫增强和抗AIV潜在佐剂的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99e4/4728501/3d3955817da2/marinedrugs-14-00004-g001.jpg

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