Purification, structural elucidation and anti-inflammatory activity in vitro of polysaccharides from Smilax china L.

多糖 鼠李糖 阿拉伯糖 半乳糖 甘露糖 化学 果胶 体外 消炎药 生物化学 立体化学 生物 木糖 药理学 发酵
作者
Yu Zhang,Xianglin Pan,Siqi Ran,Kaiping Wang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:139: 233-243 被引量:124
标识
DOI:10.1016/j.ijbiomac.2019.07.209
摘要

Smilax china L. is a traditional Chinese medicine mainly used for the treatment of pelvic inflammation. Polysaccharide might be one of the anti-inflammatory components of Smilax china L. Based on this hypothesis, this work aimed at extraction, purification and structural elucidation of Smilax china L. polysaccharides and their preliminary anti-inflammatory effects were also studied. Two polysaccharides named SCLP1 (Smilax china L. polysaccharide 1, 42.1 kDa) and SCLP3-2 (Smilax china L. polysaccharide 3-2, 16.8 kDa) were for the first time purified from Smilax china L. The structures of SCLP1 and SCLP3-2 were elucidated by chemical and spectral analysis. The results revealed that SCLP1 was a neutral polysaccharide composed of glucose and mannose (54.5:1.0). Its backbone was 1,4‑linked α‑Glcp interspersed with 1,2‑linked α‑Glcp and Manp; the branches were 1,6‑linked α-Glcp and terminated with α‑Glcp. SCLP3-2 was composed of galacturonic acid, arabinose, galactose and rhamnose (23.3:2.1:1.7:1.0) and was a pectin-type polysaccharide with an α‑1,4‑linked homogalacturonan backbone which was partially methyl-esterified and slightly acetylated. The side chains consisted of α‑Rhap, β‑Galp and α‑Araf. SCLP1 and SCLP3-2 could inhibit the production of NO, IL-6 and TNF-α in LPS-stimulated RAW264.7 cells via NF-κB and MAPKs (ERK1/2, JNK) pathways, indicating that they possessed a potential anti-inflammatory activity.
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