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西洋参中性多糖的结构表征及抗炎活性。

Structural characterization and anti-inflammatory activity of neutral polysaccharides from American ginseng.

机构信息

School of Pharmaceutical Sciences, Shandong University of Traditional Chinese Medicine, Jinan 250014, China; Biological Engineering Technology Innovation Center of Shandong Province, Heze Branch of Qilu University of Technology (Shandong Academy of Sciences), Heze 274000, China.

Shandong Analysis and Test Center, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250014, China.

出版信息

Int J Biol Macromol. 2023 Sep 1;248:125586. doi: 10.1016/j.ijbiomac.2023.125586. Epub 2023 Jun 26.

Abstract

American ginseng, a precious classic herbal medicine, is used extensively in China for life prolongation purpose. This study aimed to elucidate the structure and anti-inflammatory activity of a neutral polysaccharide isolated from American ginseng (AGP-A). Nuclear magnetic resonance in conjunction with gas chromatography-mass spectrometry were used to analyze AGP-A's structure, whereas Raw264.7 cell and zebrafish models were employed to assess its anti-inflammatory activity. According to the results, AGP-A has a molecular weight of 5561 Da and is primarily consisted of glucose. Additionally, linear α-(1 → 4)-glucans with α-D-Glcp-(1 → 6)-α-Glcp-(1→ residues linked to the backbone at C-6 formed the backbone of AGP-A. Furthermore, AGP-A significantly decreased pro-inflammatory cytokines (IL-1β, IL-6 and TNF-α) in Raw264.7 cell model. AGP-A in zebrafish model significantly lower the massive recruitment of neutrophils to the neuromast of the caudal lateral line. Inflammation may be relieved by the AGP-A component in American ginseng based on these results. In conclusion, our study shows the structural characterization, remarkable anti-inflammatory properties of AGP-A and its potential curative efficacy as a safe, valid natural anti-inflammatory medicine.

摘要

花旗参,一种珍贵的经典草药,在中国被广泛用于延长寿命。本研究旨在阐明从花旗参(AGP-A)中分离得到的中性多糖的结构和抗炎活性。采用核磁共振结合气相色谱-质谱联用技术分析 AGP-A 的结构,并用 Raw264.7 细胞和斑马鱼模型评估其抗炎活性。结果表明,AGP-A 的分子量为 5561 Da,主要由葡萄糖组成。此外,线性α-(1→4)-葡聚糖以α-D-Glcp-(1→6)-α-Glcp-(1→残基连接到 C-6 上的主链形成 AGP-A 的主链。此外,AGP-A 可显著降低 Raw264.7 细胞模型中的促炎细胞因子(IL-1β、IL-6 和 TNF-α)。AGP-A 在斑马鱼模型中可显著减少中性粒细胞向尾侧侧线神经丘的大量募集。根据这些结果,AGP-A 成分可能通过减轻炎症来发挥作用。综上所述,本研究表明 AGP-A 具有结构特征、显著的抗炎特性及其作为一种安全、有效的天然抗炎药物的潜在治疗功效。

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