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低聚果糖通过调节肠道微生物群改善 APP/PS1 转基因小鼠的认知缺陷和神经退行性变。

Fructooligosaccharides Ameliorating Cognitive Deficits and Neurodegeneration in APP/PS1 Transgenic Mice through Modulating Gut Microbiota.

机构信息

Department of Neurology , the Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University , Wenzhou , Zhejiang 325027 , China.

Department of Neurology, The Affiliated Taizhou Hospital , Wenzhou Medical University , 150# Ximen Road , Linhai District, Taizhou 317000 , Zhejiang China.

出版信息

J Agric Food Chem. 2019 Mar 13;67(10):3006-3017. doi: 10.1021/acs.jafc.8b07313. Epub 2019 Feb 28.

DOI:10.1021/acs.jafc.8b07313
PMID:30816709
Abstract

Alzheimer's disease (AD) is closely related to gut microbial alteration. Prebiotic fructooligosaccharides (FOS) play major roles by regulating gut microbiota. The present study aimed to explore the effect and mechanism of FOS protection against AD via regulating gut microbiota. Male Apse/PSEN 1dE9 (APP/PS1) transgenic (Tg) mice were administrated with FOS for 6 weeks. Cognitive deficits and amyloid deposition were evaluated. The levels of synaptic plasticity markers including postsynaptic density protein 95 (PSD-95) and synapsin I, as well as phosphorylation of c-Jun N-terminal kinase (JNK), were determined. The intestinal microbial constituent was detected by 16S rRNA sequencing. Moreover, the levels of glucagon-like peptide-1 (GLP-1) in the gut and GLP-1 receptor (GLP-1R) in the brain were measured. The results indicated that FOS treatment ameliorated cognitive deficits and pathological changes in the Tg mice. FOS significantly upregulated the expression levels of synapsin I and PSD-95, as well as decreased phosphorylated level of JNK. The sequencing results showed that FOS reversed the altered microbial composition. Furthermore, FOS increased the level of GLP-1 and decreased the level of GLP-1R in the Tg mice. These findings indicated that FOS exerted beneficial effects against AD via regulating the gut microbiota-GLP-1/GLP-1R pathway.

摘要

阿尔茨海默病(AD)与肠道微生物改变密切相关。益生元果寡糖(FOS)通过调节肠道微生物群发挥主要作用。本研究旨在通过调节肠道微生物群来探索 FOS 对 AD 的保护作用及其机制。雄性 Apse/PSEN1dE9(APP/PS1)转基因(Tg)小鼠给予 FOS 处理 6 周。评估认知缺陷和淀粉样蛋白沉积。测定突触可塑性标志物包括后突触密度蛋白 95(PSD-95)和突触素 I 以及 c-Jun N 末端激酶(JNK)磷酸化的水平。通过 16S rRNA 测序检测肠道微生物组成。此外,测量肠道中的胰高血糖素样肽-1(GLP-1)和大脑中的 GLP-1 受体(GLP-1R)的水平。结果表明,FOS 处理改善了 Tg 小鼠的认知缺陷和病理变化。FOS 显著上调突触素 I 和 PSD-95 的表达水平,并降低 JNK 的磷酸化水平。测序结果表明,FOS 逆转了改变的微生物组成。此外,FOS 增加了 Tg 小鼠中 GLP-1 的水平并降低了 GLP-1R 的水平。这些发现表明,FOS 通过调节肠道微生物群-GLP-1/GLP-1R 途径对 AD 发挥有益作用。

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