研究40hz声刺激对阿尔茨海默病通路的影响:淀粉样蛋白-β42分泌、tau磷酸化、吞噬和自噬的调节。

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Yuan-Han Yang, Hsi-Wen Chang, Ching-Fang Chien, Tzyh-Chyuan Hour
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引用次数: 0

摘要

阿尔茨海默病(AD)是老龄化社会中痴呆症的主要原因。先前的研究表明,非侵入性的闪烁和伽马频率振荡的声音可以调节AD小鼠的AD相关病理,潜在地改善患者的预后。然而,伽马频率振荡的声音抑制淀粉样蛋白-β1-42 (Aβ42)的表达和tau蛋白的磷酸化,以及调节神经细胞自噬的分子机制尚不清楚。目的探讨40 Hz声刺激对ad相关通路的分子效应。方法设计40 Hz刺激声(H+多频音频),细胞暴露于H+多频音频中。酶联免疫吸附法测定Aβ42的浓度。western blotting检测蛋白水平。用共聚焦显微镜和吞噬分析检查吞噬作用。结果首先,我们发现暴露在40 Hz的刺激声中,通过激活AβPP/ADAM10通路和抑制AβPP/BACE1通路,抑制了Aβ42的分泌。其次,通过Akt/mTOR通路失活,40 Hz的刺激声抑制了Thr181位点的tau磷酸化。第三,40 Hz刺激声通过AMPK/ULK/LC3B通路增强细胞中Aβ42的吞噬和自噬。结论研究表明,40hz刺激声参与抑制细胞Aβ42分泌、p-Tau蛋白表达,促进细胞吞噬和Aβ42自噬。我们建议40hz的刺激声可能是一种潜在的干预措施,以减弱AD的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating the effects of 40 Hz sound stimulation on Alzheimer's disease pathways: Modulation of amyloid-β42 secretion, tau phosphorylation, phagocytosis, and autophagy.

BackgroundAlzheimer's disease (AD) is the main cause of dementia in an aging society. Previous studies have demonstrated that non-invasive light flicker and sound with gamma frequency oscillations can modulate AD-related pathology in AD mice, potentially improving patient outcomes. However, the molecular mechanism by which sound with gamma frequency oscillations inhibits the expression of amyloid-β1-42 (Aβ42) and the phosphorylation of tau, and modulating cell autophagy in nerve cells are still unclear.ObjectiveThis study aimed to explore the molecular effects of 40 Hz sound stimulation on AD-related pathways in a cellular model.MethodsWe designed a 40 Hz stimulating sound (H+ multi-frequency audio) for this study, and cells were exposed to H+ multi-frequency audio. The concentration of Aβ42 was quantified by enzyme-linked immunosorbent assay. Protein levels were examined by western blotting. Phagocytosis was examined by confocal microscopy and phagocytic analysis.ResultsFirst, we found that exposure to the 40 Hz stimulating sound inhibited the secretion of Aβ42 by activating the AβPP/ADAM10 pathway and suppressing the AβPP/BACE1 pathway. Second, 40 Hz stimulating sound inhibited tau phosphorylation at Thr181 through the inactivation of the Akt/mTOR pathway. Third, 40 Hz stimulating sound enhanced the phagocytosis and autophagy of Aβ42 through the AMPK/ULK/LC3B pathway in cells.ConclusionsOur study showed that 40 Hz stimulating sound is involved in the inhibition of Aβ42 secretion, p-Tau protein expression, and the promotion of phagocytosis and Aβ42 autophagy in cells. We suggest that 40 Hz stimulating sound could be a potential intervention to attenuate AD progression in the future.

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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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