Sericultural & Agri-Food Research Institute, Guangdong Academy of Agricultural Sciences/Key Laboratory of Functional Foods, Ministry of Agriculture and Rural Affairs/Guangdong Key Laboratory of Agricultural Products Processing, Guangzhou 510610, PR China.
Sericultural & Agri-Food Research Institute, Guangdong Academy of Agricultural Sciences/Key Laboratory of Functional Foods, Ministry of Agriculture and Rural Affairs/Guangdong Key Laboratory of Agricultural Products Processing, Guangzhou 510610, PR China.
Carbohydr Polym. 2020 Oct 15;246:116532. doi: 10.1016/j.carbpol.2020.116532. Epub 2020 Jun 17.
In this study, LPIIa, a purified polysaccharide from longan pulp, was isolated. Its anti-inflammatory activity and intestinal barrier protection were investigated with LPS-treated co-culture model of Caco-2 cells and RAW 264.7 macrophages. The average molecular weight LPIIa was 159.3 kDa. Its detailed structure was shown below. The backbone of LPIIa was composed of (1→3,4)-linked-α-Rhap, (1→4)-linked-β-Galp, (1→6)-linked-β-Galp, and (1→3,6)-linked-β-Galp, with branches at the O-4 of Rha and O-3 of Gal, consisting of side chains of α-Araf, β-Galp, and α-Glcp. In LPS-induced RAW 264.7 macrophages, LPIIa suppressed the production of inflammatory mediators, including TNF-α, IL-6, NO, and PGE2, and inhibited iNOS and COX-2 gene expression. In addition, LPIIa attenuated intestinal tight-junctional channel protein Claudin-2 expression and increased tight-junctional barrier protein ZO-1 expression in Caco-2 cells. Knowing the structural features and activities of longan polysaccharide gives insights into longan polysaccharide application as an anti-inflammatory agent or adjuvant in curing the intestinal inflammation.
在这项研究中,从桂圆果肉中分离出一种纯化的多糖 LPIIa。采用 LPS 处理的 Caco-2 细胞和 RAW 264.7 巨噬细胞共培养模型,研究了其抗炎活性和肠道屏障保护作用。LPIIa 的平均分子量为 159.3 kDa。其详细结构如下。LPIIa 的骨架由 (1→3,4)-连接的-α-Rhap、(1→4)-连接的-β-Galp、(1→6)-连接的-β-Galp 和 (1→3,6)-连接的-β-Galp 组成,在 Rha 的 O-4 和 Gal 的 O-3 处带有支链,由α-Araf、β-Galp 和α-Glcp 的侧链组成。在 LPS 诱导的 RAW 264.7 巨噬细胞中,LPIIa 抑制了 TNF-α、IL-6、NO 和 PGE2 等炎症介质的产生,并抑制了 iNOS 和 COX-2 基因的表达。此外,LPIIa 减弱了 Caco-2 细胞中紧密连接通道蛋白 Claudin-2 的表达,增加了紧密连接屏障蛋白 ZO-1 的表达。了解龙眼多糖的结构特征和活性,可为龙眼多糖作为抗炎剂或佐剂治疗肠道炎症提供参考。