Meng Fa-Yan, Ning Yuan-Ling, Qi Jia, He Zhou, Jie Jiang, Lin Juan-Juan, Huang Yan-Jun, Li Fu-Sen, Li Xue-Hua
School of Pharmaceutical Sciences, Guangxi Medical University, No. 22 Shuangyong Road, Nanning 530021, Guangxi, China.
Department of Pharmacy, Heilongjiang Nursing College, No. 209 Xuefu Road, Harbin 150036, Heilongjiang, China.
Int J Mol Sci. 2014 Mar 24;15(3):5140-62. doi: 10.3390/ijms15035140.
A new water-soluble polysaccharide (longan polysaccharide 1 (LP1)) was extracted and successfully purified from Dimocarpus longan pulp via diethylaminoethyl (DEAE)-cellulose anion-exchange and Sephacryl S-300 HR gel chromatography. The chemical structure was determined using Infrared (IR), gas chromatography (GC) and nuclear magnetic resonance (NMR) analysis. The results indicated that the molecular weight of the sample was 1.1 × 10(5) Da. Monosaccharide composition analysis revealed that LP1 was composed of Glc, GalA, Ara and Gal in a molar ratio of 5.39:1.04:0.74:0.21. Structural analysis indicated that LP1 consisted of a backbone of → 4)-α-D-Glcp-(1 → 4)-α-D-GALPA-(1 → 4)-α-D-Glcp-(1 → 4)-β-D-Glcp-(1 → units with poly saccharide side chains composed of → 2)-β-D-Fruf-(1 → 2)-L-sorbose-(1 → attached to the O-6 position of the α-D-Glcp residues. In vitro experiments indicated that LP1 had significantly high antitumor activity against SKOV3 and HO8910 tumor cells, with inhibition percentages of 40% and 50%, respectively. In addition, LP1 significantly stimulated the production of the cytokine interferon-γ (IFN-γ), increased the activity of murine macrophages and enhanced B- and T-lymphocyte proliferation. The results of this study demonstrate that LP1 has potential applications as a natural antitumor agent with immunomodulatory activity.
从龙眼果肉中通过二乙氨基乙基(DEAE)-纤维素阴离子交换和Sephacryl S-300 HR凝胶色谱法提取并成功纯化出一种新的水溶性多糖(龙眼多糖1(LP1))。使用红外(IR)、气相色谱(GC)和核磁共振(NMR)分析确定其化学结构。结果表明该样品的分子量为1.1×10⁵ Da。单糖组成分析显示LP1由葡萄糖(Glc)、半乳糖醛酸(GalA)、阿拉伯糖(Ara)和半乳糖(Gal)组成,摩尔比为5.39:1.04:0.74:0.21。结构分析表明LP1由→4)-α-D-葡萄糖-(1→4)-α-D-半乳糖醛酸-(1→4)-α-D-葡萄糖-(1→4)-β-D-葡萄糖-(1→单元的主链组成,其多糖侧链由→2)-β-D-呋喃果糖-(1→2)-L-山梨糖-(1→连接到α-D-葡萄糖残基的O-6位。体外实验表明LP1对SKOV3和HO8910肿瘤细胞具有显著的高抗肿瘤活性,抑制率分别为40%和50%。此外,LP1显著刺激细胞因子干扰素-γ(IFN-γ)的产生,增加小鼠巨噬细胞的活性并增强B淋巴细胞和T淋巴细胞的增殖。本研究结果表明LP1作为具有免疫调节活性的天然抗肿瘤剂具有潜在应用价值。