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沙棘多糖通过调节肠道菌群失调改善高脂饮食诱导的小鼠神经炎症和突触功能障碍。

Sea buckthorn polysaccharide ameliorates high-fat diet induced mice neuroinflammation and synaptic dysfunction via regulating gut dysbiosis.

作者信息

Lan Ying, Ma Zhiyuan, Chang Lili, Peng Jing, Zhang Mengqi, Sun Qingyang, Qiao Ruixue, Hou Xinglin, Ding Xuechao, Zhang Qiang, Peng Qiang, Dong Juane, Liu Xuebo

机构信息

College of Food Science and Engineering, Northwest A&F University, Yangling 712100, Shaanxi, China.

College of Food Science and Engineering, Northwest A&F University, Yangling 712100, Shaanxi, China; College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China.

出版信息

Int J Biol Macromol. 2023 May 1;236:123797. doi: 10.1016/j.ijbiomac.2023.123797. Epub 2023 Feb 23.

Abstract

Currently, definitive treatment for neurodegenerative diseases without side effects has not been developed, therefore, exploring natural polysaccharides with neuroprotection to prevent the occurrences and progressions of cognitive dysfunctions has important significance. The purpose of this study was to investigate the effects of sea buckthorn polysaccharide (SBP) on high-fat diet (HFD) induced mice cognitive dysfunctions and attempted to explore its biological mechanisms. Behavior tests (Y-maze and Barnes maze) suggested that SBP effectively alleviated the HFD induced behavioral disorders, which was in accordance with the inhibition of neuroinflammation via suppressing the NF-κB pathway and amelioration of synaptic dysfunction via upregulating CREB/BDNF/TrkB pathway in mice brain. Furthermore, SBP alleviated the gut barrier impairment, inflammatory responses, and lipopolysaccharide invasion into blood circulation via regulating the gut microbiome structure, especially correcting the reduction of Ileibacterium and increase of Lactobacillus, Dubosiella, Olsenella, Helicobacter, and Ruminiclostridium_9 in HFD mice. Therefore, the reversal effects of SBP on gut dysbiosis might be the important reason for its positive effects on cognitive dysfunction induced by HFD in mice.

摘要

目前,尚未开发出无副作用的神经退行性疾病的确定性治疗方法,因此,探索具有神经保护作用的天然多糖以预防认知功能障碍的发生和发展具有重要意义。本研究的目的是研究沙棘多糖(SBP)对高脂饮食(HFD)诱导的小鼠认知功能障碍的影响,并试图探索其生物学机制。行为测试(Y迷宫和巴恩斯迷宫)表明,SBP有效减轻了HFD诱导的行为障碍,这与通过抑制NF-κB途径抑制神经炎症以及通过上调小鼠大脑中的CREB/BDNF/TrkB途径改善突触功能障碍相一致。此外,SBP通过调节肠道微生物群结构减轻了肠道屏障损伤、炎症反应和脂多糖侵入血液循环,特别是纠正了HFD小鼠中回肠杆菌的减少以及乳酸杆菌、杜氏菌、奥尔森菌、幽门螺杆菌和瘤胃梭菌_9的增加。因此,SBP对肠道菌群失调的逆转作用可能是其对HFD诱导的小鼠认知功能障碍产生积极影响的重要原因。

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