病态的
肠道菌群
认知障碍
药理学
肠-脑轴
医学
神经科学
传统医学
认知
生物
病理
免疫学
作者
Wei Zhao,Jianhui Wang,Maria Latta,Chenyu Wang,Yuheng Liu,Wantong Ma,Zhaoyang Zhou,Shujian Hu,Peng Chen,Ying‐Qian Liu
标识
DOI:10.3389/fphar.2022.903659
摘要
Gastrodiae Rhizoma and its active constituents are known to exhibit neuroprotective effects in Alzheimer’s disease (AD). However, the effect of Rhizoma Gastrodiae water extract (WERG) on AD and the detailed mechanism of action remain unclear. In this study, the mechanism of action of WERG was investigated by the microbiome–gut–brain axis using a D-galactose (D-gal)/AlCl 3 -induced AD mouse model. WERG improved the cognitive impairment of D-gal/AlCl 3 -induced mice. The expression level of p-Tau thr231 in the WERG-H treatment group was decreased, and p-Tau thr231 was found negative in hippocampal DG, CA1, and CA3 regions. Here, the diversity and composition of the gut microbiota were analyzed by 16sRNA sequencing. WERG-H treatment had a positive correlation with Firmicutes, Bacilli, Lactobacillus johnsonii , Lactobacillus murinus , and Lactobacillus reuteri . Interestingly, the Rikenellaceae-RC9 gut group in the gut increased in D-gal/AlCl 3 -induced mice, but the increased L. johnsonii , L. murinus , and L. reuteri reversed this process. This may be a potential mechanistic link between gut microbiota dysbiosis and P-Tau Thr231 levels in AD progression. In conclusion, this study demonstrated that WERG improved the cognitive impairment of the AD mouse model by enriching gut probiotics and reducing P-Tau Thr231 levels.
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