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扶正祛邪方通过降低Tau蛋白过度磷酸化改善SAMP8小鼠的学习记忆障碍

Fuzheng Quxie Decoction Ameliorates Learning and Memory Impairment in SAMP8 Mice by Decreasing Tau Hyperphosphorylation.

作者信息

Yang Yang, Jia Xingxing, Feng Jianchao, Wang Zhiyong, Cao Yu, Liu Jiangang, Li Hao

机构信息

Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.

Graduate School, Beijing University of Chinese Medicine, Beijing 100029, China.

出版信息

Evid Based Complement Alternat Med. 2017;2017:5934254. doi: 10.1155/2017/5934254. Epub 2017 Dec 20.

DOI:10.1155/2017/5934254
PMID:29422936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5750500/
Abstract

Hyperphosphorylation of the microtubule-associated protein, tau, is critical to the progression of Alzheimer's disease (AD). Fuzheng Quxie Decoction (FQD), a Chinese herbal complex, is an effective clinical formula used to treat AD. In the current study, we employed high-performance liquid chromatography and liquid chromatography tandem mass spectrometry to identify the components of FQD. Three major components (ginsenoside Rg1, ginsenoside Re, and coptisine) were detected in the brain of FQD-fed mice, indicating their ability to cross the blood-brain barrier. We further evaluated the efficacy of FQD on Senescence-Accelerated Mice Prone-8 (SAMP8) mice. FQD significantly ameliorated learning and memory deficits in SAMP8 mice on the Morris Water Maze, decreasing escape latency ( < 0.01) and increasing swim time within the original platform-containing quadrant ( < 0.05). Further, FQD increased the number of neurons and intraneuronal Nissl bodies in the hippocampal CA1 region. FQD also decreased the expression of phosphorylated tau protein and increased the expression of protein phosphatase 2A (PP2A) and the N-methyl-D-aspartate receptor subunit, NR2A ( < 0.01). Our results indicate that FQD improves the learning and memory ability of SAMP8 mice. Moreover, our findings suggest that the protective effect of FQD is likely mediated through an inhibition of hippocampal tau hyperphosphorylation via NMDAR/PP2A-associated proteins.

摘要

微管相关蛋白tau的过度磷酸化对阿尔茨海默病(AD)的进展至关重要。扶正祛邪汤(FQD)是一种中药复方,是治疗AD的有效临床方剂。在本研究中,我们采用高效液相色谱和液相色谱串联质谱法鉴定FQD的成分。在喂食FQD的小鼠脑中检测到三种主要成分(人参皂苷Rg1、人参皂苷Re和黄连碱),表明它们能够穿过血脑屏障。我们进一步评估了FQD对衰老加速小鼠易感8型(SAMP8)小鼠的疗效。FQD显著改善了SAMP8小鼠在莫里斯水迷宫中的学习和记忆缺陷,减少了逃避潜伏期(<0.01),并增加了在含原始平台象限内的游泳时间(<0.05)。此外,FQD增加了海马CA1区神经元和神经元内尼氏体的数量。FQD还降低了磷酸化tau蛋白的表达,并增加了蛋白磷酸酶2A(PP2A)和N-甲基-D-天冬氨酸受体亚基NR2A的表达(<0.01)。我们的结果表明,FQD提高了SAMP8小鼠的学习和记忆能力。此外,我们的研究结果表明,FQD的保护作用可能是通过NMDAR/PP2A相关蛋白抑制海马tau过度磷酸化来介导的。

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本文引用的文献

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Behav Brain Res. 2016 Jul 15;308:187-95. doi: 10.1016/j.bbr.2016.04.026. Epub 2016 Apr 16.
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The Role of Berberine in the Multi-Target Treatment of Senile Dementia.黄连素在老年痴呆多靶点治疗中的作用
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Inhibition of Protein Phosphatase 2A: Focus on the Glutamatergic System.蛋白磷酸酶2A的抑制作用:聚焦于谷氨酸能系统。
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Integrated Network Pharmacology and Comprehensive Bioinformatics Identifying the Mechanisms and Molecular Targets of Yizhiqingxin Formula for Treatment of Comorbidity With Alzheimer's Disease and Depression.整合网络药理学与综合生物信息学方法探究益智清心方治疗阿尔茨海默病合并抑郁症共病的作用机制及分子靶点
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Neuroprotective Potentials of Panax Ginseng Against Alzheimer's Disease: A Review of Preclinical and Clinical Evidences.人参对阿尔茨海默病的神经保护潜力:临床前和临床证据综述
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