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EPRCN通过调节肠道微生物群和恢复阿尔茨海默病模型小鼠的肠道免疫稳态发挥神经保护作用。

EPRCN exerts neuroprotective function by regulating gut microbiota and restoring gut immune homeostasis in Alzheimer's disease model mice.

作者信息

Li Ming-Jie, Lan Meng-Ning, Du Yao-Xuan, Liu Yue, Zhang Hua-Yue, Guo Min, Liu Shi-Wei, Xia Hai-Yang, Wu Zheng-Jun, Zheng Hua-Jun

机构信息

College of Food Science and Technology, Shanghai Ocean University, Shanghai, China.

Shanghai-MOST Key Laboratory of Health and Disease Genomics, NHC Key Lab of Reproduction Regulation, Shanghai Institute for Biomedical and Pharmaceutical Technologies, Shanghai, China.

出版信息

J Alzheimers Dis. 2025 Jul;106(1):151-166. doi: 10.1177/13872877251339762. Epub 2025 May 5.

Abstract

BackgroundNo effective drug treatment is currently available for Alzheimer's disease (AD), highlighting the urgent need to develop efficient therapeutic options. We have developed a formula based on medicine and food homology (MFH) consisting of egg yolk oil, perilla seed oil, raphani seed oil, cinnamon oil, and noni puree (EPRCN), and demonstrated that it can treat AD by alleviating neuroinflammation and oxidative stress. However, whether EPRCN can improve AD by regulating gut microbiota remains unknown.ObjectiveThe current study aimed to evaluate the effect of EPRCN on regulating gut microbiota and neuroprotection.Methods16S rRNA sequencing was used to assess the structure of gut microbiota. Hematoxylin-eosin (HE) staining, qRT-PCR, and ELISA were used to evaluate gut inflammation. Detected indexes associated with cholinergic dysfunction and neuronal damage to investigate the neuroprotective effects of EPRCN.Results16S rRNA gene analysis revealed that EPRCN remodeled the gut microbiota, inhibited gut metabolic disorders, and promoted CoA biosynthesis in scopolamine-induced mice. EPRCN can ameliorates gut inflammation by activating the cholinergic anti-inflammatory pathway. The results further indicated that EPRCN improved cholinergic dysfunction by inhibiting the activity of acetylcholinesterase and restoring cholinergic receptors. Additionally, EPRCN administration suppressed the neuronal loss and elevated brain derived neurotrophic factor expression in hippocampus. Correlation analysis found that alteration of several gut microbes was associated with indexes improved by EPRCN.ConclusionsThese findings suggest that EPRCN may serve as a promising dietary intervention for treating AD by regulating the microbiota-gut-brain axis and exerting neuroprotective function.

摘要

背景

目前尚无有效的药物治疗阿尔茨海默病(AD),这凸显了开发有效治疗方案的迫切需求。我们开发了一种基于药食同源(MFH)的配方,由蛋黄油、紫苏籽油、莱菔子油、肉桂油和诺丽果泥(EPRCN)组成,并证明它可以通过减轻神经炎症和氧化应激来治疗AD。然而,EPRCN是否能通过调节肠道微生物群来改善AD仍不清楚。

目的

本研究旨在评估EPRCN对调节肠道微生物群和神经保护的作用。

方法

采用16S rRNA测序评估肠道微生物群的结构。苏木精-伊红(HE)染色、qRT-PCR和ELISA用于评估肠道炎症。检测与胆碱能功能障碍和神经元损伤相关的指标,以研究EPRCN的神经保护作用。

结果

16S rRNA基因分析显示,EPRCN重塑了肠道微生物群,抑制了肠道代谢紊乱,并促进了东莨菪碱诱导小鼠的辅酶A生物合成。EPRCN可通过激活胆碱能抗炎途径改善肠道炎症。结果进一步表明,EPRCN通过抑制乙酰胆碱酯酶活性和恢复胆碱能受体来改善胆碱能功能障碍。此外,给予EPRCN可抑制神经元丢失并提高海马中脑源性神经营养因子的表达。相关性分析发现,几种肠道微生物的改变与EPRCN改善的指标相关。

结论

这些发现表明,EPRCN可能是一种有前景的饮食干预措施,通过调节微生物群-肠道-脑轴并发挥神经保护功能来治疗AD。

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