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五味子多糖的纯化、结构表征及认知改善活性。

Purification, structural characterization, and cognitive improvement activity of a polysaccharides from Schisandra chinensis.

机构信息

School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang 110016, China.

School of Functional Food and Wine, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang 110016, China.

出版信息

Int J Biol Macromol. 2020 Nov 15;163:497-507. doi: 10.1016/j.ijbiomac.2020.06.275. Epub 2020 Jul 3.

Abstract

The present study aimed to evaluate structural characteristics of a polysaccharides, SCP2-1, isolated from Schisandra chinensis (Turcz.) Baill (S. chinensis) and to assess its improvement on cognitive dysfunction caused by excessive neuroinflammation. Structural characterization indicated that SCP2-1 was composed of glucose and galactose in a molar ratio of 8.78:1.23 with molecular weight of 5.388 kDa. The main linkages of the glycosidic bonds of SCP2-1were 1,4-linked-Glcp, 1,4-linked-Galp, 1-linked-Galp and 1,4,6-linked-Galp. The evaluation of behavioral pharmacology and the detection of biochemical markers exhibited that SCP2-1 could improve LPS-induced cognitive dysfunction in mice, ameliorate excessive inflammatory response. The results showed that SCP2-1 could ameliorated the animals' exploration time of novel arm in Y maze test, shortened the escape latency of mice in MWM test, and increased the exploration time of new object in NOR test. What's more, mice could improve histopathological changes induced by LPS, suppress the over-activation of glial cells, decrease the expression of proinflammatory cytokines, increase the levels of anti-inflammatory cytokines, reduce the levels of NLRP3, M-caspaes-1, which may further induce the decrease of excessive deposition of Aβ. Furthermore, SCP2-1 could inhibit the over-activation of NF-κB and the hyperphosphorylation of P38 MAPK pathway.

摘要

本研究旨在评估五味子多糖 SCP2-1 的结构特征,并评估其对过度神经炎症引起的认知功能障碍的改善作用。结构表征表明,SCP2-1 由葡萄糖和半乳糖组成,摩尔比为 8.78:1.23,分子量为 5.388 kDa。SCP2-1 的糖苷键的主要连接方式为 1,4-连接-Glcp、1,4-连接-Galp、1-连接-Galp 和 1,4,6-连接-Galp。行为药理学评价和生化标志物检测表明,SCP2-1 可改善 LPS 诱导的小鼠认知功能障碍,减轻过度炎症反应。结果表明,SCP2-1 可改善 Y 迷宫试验中小鼠新臂探索时间,缩短 MWM 试验中小鼠逃避潜伏期,增加 NOR 试验中新物体探索时间。此外,SCP2-1 可改善 LPS 诱导的组织病理学变化,抑制神经胶质细胞过度激活,降低促炎细胞因子表达,增加抗炎细胞因子水平,降低 NLRP3、M-caspaes-1 水平,从而进一步减少 Aβ 的过度沉积。此外,SCP2-1 可抑制 NF-κB 的过度激活和 P38 MAPK 通路的过度磷酸化。

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