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天麻中不同分子量和结构特征多糖的体外和体内免疫增强作用

In vitro and in vivo immune-enhancing effects of polysaccharides with different molecular weights and structural characteristics from Gastrodia elata Blume.

作者信息

Chen Jia-Qian, Yuan Wei-Yuan, Miao Wen, Gong Shi-Lin, Zhou Jie, Liu Ying, Wu Jian-Lin, Li Na

机构信息

State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Taipa, Macao.

Zhuhai & University of Macau Science and Technology Research Institute, Zhuhai 519000, PR China.

出版信息

Int J Biol Macromol. 2025 Mar;295:139526. doi: 10.1016/j.ijbiomac.2025.139526. Epub 2025 Jan 7.

DOI:10.1016/j.ijbiomac.2025.139526
PMID:39788267
Abstract

Research on high-molecular-weight polysaccharides tends to be more difficult and lag in terms of their fine structures and bioavailability. We focused on Gastrodia elata Blume polysaccharides (GEPs) with different molecular weights and structural characteristics to reveal their bioactivities, especially those abundant high-molecular-weight GEPs. A novel high-yield polysaccharide (GEP1-2) with the high molecular weight of 3.21 × 10 Da was first purified. Through conventional and enzymolysis-assisted analyses, GEP1-2 was an α-D-(1,4)(1,6)-glucan with unique linkages of →2)-β-D-Frucf-(1→, →4)-β-D-Glcp-(1→ and p-hydroxybenzyl alcohol citrate (HAC), and its main local fine structure had α-1-Glcp, α-1,4-Glcp, α-1,6-Glcp, β-1,6-Galp, and α-1,4,6-Glcp at the molar ratio of 1.20∶17.74∶2.71∶0.98∶0.76. Another refined GEP3-3 with 1.91 × 10 Da was identified as an α-1,4- and α-1,4,6-glucan (molar ratio of 4.91∶1.02). It was noteworthy that all GEPs could induce the release and mRNA expressions of NO and cytokines in RAW264.7 macrophages. Specially, the high-molecular-weight polysaccharides showed comparable in vitro immune-enhancing effects to the low-molecular-weight polysaccharide. Furthermore, the macromolecular GEP1-2 could dose-dependently increase the organ coefficient of thymus and cytokine levels of TNF-α and IL-6 in mouse serum as well as in splenic lymphocytes. These efforts will be of great significance when proceeding to the safe relief or therapy of macromolecular GEPs for immunologic diseases.

摘要

对高分子量多糖的研究在其精细结构和生物利用度方面往往更具难度且滞后。我们聚焦于具有不同分子量和结构特征的天麻多糖(GEPs),以揭示其生物活性,尤其是那些丰富的高分子量GEPs。首先纯化出一种分子量为3.21×10 Da的新型高产多糖(GEP1-2)。通过常规分析和酶解辅助分析,GEP1-2是一种α-D-(1,4)(1,6)-葡聚糖,具有独特的→2)-β-D-Frucf-(1→、→4)-β-D-Glcp-(1→连接以及对羟基苄醇柠檬酸盐(HAC),其主要局部精细结构具有摩尔比为1.20∶17.74∶2.71∶0.98∶0.76的α-1-Glcp、α-!,4-Glcp、α-1,6-Glcp、β-1,6-Galp和α-1,4,6-Glcp。另一种纯化的分子量为1.91×10 Da的GEP3-3被鉴定为α-1,4-和α-1,4,6-葡聚糖(摩尔比为4.91∶1.02)。值得注意的是,所有GEPs均可诱导RAW264.7巨噬细胞中NO和细胞因子的释放及mRNA表达。特别地,高分子量多糖在体外显示出与低分子量多糖相当的免疫增强作用。此外,大分子GEP1-2可剂量依赖性地增加小鼠血清以及脾淋巴细胞中胸腺的器官系数以及TNF-α和IL-6的细胞因子水平。在推进对免疫疾病进行高分子量GEPs的安全缓解或治疗时,这些研究将具有重要意义。

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