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人参皂苷 Rg1 可改善认知能力,并影响阿尔茨海默病树鼩模型的大肠微生物群。

Ginsenoside Rg1 improves cognitive capability and affects the microbiota of large intestine of tree shrew model for Alzheimer's disease.

机构信息

Department of Laboratory Animal Science, Kunming Medical University, Kunming, Yunnan 650500, P.R. China.

Technology Transfer Center, Kunming Medical University, Kunming, Yunnan 650500, P.R. China.

出版信息

Mol Med Rep. 2021 Apr;23(4). doi: 10.3892/mmr.2021.11931. Epub 2021 Mar 2.

DOI:10.3892/mmr.2021.11931
PMID:33649817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7930927/
Abstract

Ginsenoside Rg1 (Rg1) is traditional Chinese medicine with neuroprotective activity. Previous studies have demonstrated that Rg1 improves Alzheimer's disease (AD) and alters gut microbiology, but its mechanism remains to be elucidated, and thus far, its use in the treatment of AD has not been satisfactory. The present study investigated the improvement effects of Rg1 and its association with the microbiota of the large intestine. Following treatment with Rg1 in AD tree shrews, the treatment group demonstrated significantly shorter escape latency and crossed a platform more frequently in a water maze test. Western blotting demonstrated that Rg1 inhibited the expression of β-secretase 1, while increasing microtubule-associated protein 2 and Fox-3 in the hippocampus. Immunohistochemical analysis revealed that Rg1 decreased the expression of amyloid β, tau phosphorylated at serine 404 and pro-apoptotic factor Bax, while increasing the expression of Bcl-2 in the hippocampus and cortex. High throughput sequencing of 16S rRNA demonstrated that Rg1 altered the microbiota abundance of the large intestine. In conclusion, Rg1 affected the expression of apoptosis proteins, possessed a neuroprotective effect and may have a close association with the microbiota of large intestine by significantly reducing the abundance of and increasing the energy requirement of tree shrews.

摘要

人参皂苷 Rg1(Rg1)是一种具有神经保护活性的中药。先前的研究表明,Rg1 可改善阿尔茨海默病(AD)并改变肠道微生物群,但它的作用机制仍有待阐明,迄今为止,其在 AD 治疗中的应用并不令人满意。本研究探讨了 Rg1 的改善作用及其与大肠微生物群的关系。在 AD 树鼩中用 Rg1 治疗后,治疗组在水迷宫测试中表现出明显更短的逃避潜伏期和更频繁地穿过平台。Western blot 表明,Rg1 抑制了 β-分泌酶 1 的表达,同时增加了海马体中的微管相关蛋白 2 和 Fox-3。免疫组织化学分析显示,Rg1 降低了海马体和皮质中淀粉样β、丝氨酸 404 磷酸化的 tau 和促凋亡因子 Bax 的表达,同时增加了 Bcl-2 的表达。16S rRNA 的高通量测序表明,Rg1 改变了大肠微生物群的丰度。总之,Rg1 影响了凋亡蛋白的表达,具有神经保护作用,并且通过显著降低的丰度和增加树鼩的能量需求,与大肠微生物群可能密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/b5c7af1072de/mmr-23-04-11931-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/6fc0ca2f530b/mmr-23-04-11931-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/039c834b9c36/mmr-23-04-11931-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/af1b0399bb3a/mmr-23-04-11931-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/d7aa29350dec/mmr-23-04-11931-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/b5c7af1072de/mmr-23-04-11931-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/6fc0ca2f530b/mmr-23-04-11931-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/039c834b9c36/mmr-23-04-11931-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/af1b0399bb3a/mmr-23-04-11931-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/d7aa29350dec/mmr-23-04-11931-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7864/7930927/b5c7af1072de/mmr-23-04-11931-g06.jpg

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