神果种子甲醇提取物通过抑制AKT/mTOR信号通路减轻阿尔茨海默病并增强自噬。

IF 3.1 3区 医学 Q2 NEUROSCIENCES
Zi-Ting Shang, Xue-Yan Huang, Liu-Lin Xiong, Zu-Cai Xu, He-Xu Liu, Chang-Yin Yu
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引用次数: 0

摘要

背景:阿尔茨海默病(AD)是一种神经退行性疾病。在前期研究中,我们发现神果籽甲醇提取物(MFSs)对AD模型小鼠有治疗作用。目的:本研究旨在研究MFSs在减轻淀粉样蛋白-β (Aβ)沉积中的作用,并进一步探讨MFSs可能的作用机制。方法:采用行为学实验和多种免疫标记技术对2种AD模型(秀丽隐杆线虫Aβ转基因模型株CL4176和3 × Tg-AD小鼠)进行实验。结果:MFSs (10 μg/mL)能有效缓解CL4176中Aβ所致的瘫痪,使Aβ斑块明显减少,Aβ、age-1、akt-1、mTOR基因转录水平显著下调,自噬相关基因lgg-1转录增强。MFSs组小鼠的认知功能得到改善,这与减少突触丢失和脑内a β阳性神经元有关。同时,淀粉样蛋白-β前体(a -β pp)、Tau、Akt和mTOR的转录水平显著降低。PSD95、SYN1、LC3II/I、Beclin-1蛋白表达显著升高,p62/SQSTM1、p-AKT/AKT、p-mTOR/mTOR蛋白表达降低。结论:MFSs可显著减轻小鼠和CL4176体内Aβ的沉积。其改善AD小鼠认知功能的机制可能与Akt/mTOR信号通路调控的自噬增强有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methanol extract from miracle fruit seeds mitigates Alzheimer's disease and enhance autophagy via suppressing the AKT/mTOR signal pathway.

Background: Alzheimer's disease (AD) is a neurodegenerative disease. In previous study, we discovered that methanol extract of miracle fruits seeds (MFSs) had a therapeutic effect on AD model mice. Objective: In this research, we aimed to study the role of MFSs in alleviating amyloid-β (Aβ) deposition and further explore the possible mechanism of action of MFSs. Methods: We used behavioral tests and various immunolabeling techniques on two AD model (Aβ transgenic model strain CL4176 of Caenorhabditis elegans and the 3 × Tg-AD mice). Results: In CL4176, MFSs (10 μg/mL) could effectively alleviate the paralysis caused by Aβ, the Aβ plaques were significantly reduced, the transcription levels of , age-1, akt-1 and mTOR genes were significantly downregulated, and the transcription of autophagy-related gene lgg-1 was enhanced. The cognitive function of mice in the MFSs group was improved, which was related to reduced synapse loss and Aβ-positive neurons in the brain. Meanwhile, the transcription levels of amyloid-β protein precursor (AβPP), Tau, Akt and mTOR were significantly reduced. The protein expressions of PSD95, SYN1, LC3II/I and Beclin-1 were significantly increased, and the value of p62/SQSTM1, p-AKT/AKT, p-mTOR/mTOR were reduced. Conclusions: MFSs significantly alleviates Aβ deposition in CL4176 and mice. The mechanism by which it improves cognitive function in AD mice may be related to enhanced autophagy regulated by the Akt/mTOR signaling pathway.

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来源期刊
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease 医学-神经科学
CiteScore
6.40
自引率
7.50%
发文量
1327
审稿时长
2 months
期刊介绍: The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.
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