一种新的中药配方通过靶向糖酵解途径和神经炎症反应来恢复APP/PS1小鼠的睡眠和认知功能。

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Jiani Zhang, Chunxiang Wang, Kexin Chang, Tiantian Peng, Chengbang Liang, Junshi Cheng, Yu Shi, Xu Wang, Zhaoyang Wang, Yan Tan, Qian Hua
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引用次数: 0

摘要

阿尔茨海默病(AD)被认为是一种多因素神经退行性疾病,涉及许多细胞和分子过程,如睡眠障碍、脑糖代谢失衡和神经炎症;这些失调通常先于症状的出现。因此,在许多病例中,AD诊断后单靶点治疗的效果并不理想。目的中药治疗阿尔茨海默病具有很大的潜力。睡眠障碍是阿尔茨海默病的早期症状之一;然而,目前还没有有效的方法来解决由AD引起的睡眠障碍。一些中药通过调节能量代谢或改善神经炎症来治疗睡眠障碍。本研究旨在探讨提前给药XX-F是否可以通过改善睡眠质量和神经炎症来缓解AD。方法小鼠ig泻心通腑方(XX-F) 3个月。Morris水迷宫和戊巴比妥诱导睡眠试验评估认知和睡眠。通过western blot和特异性检测试剂盒确定糖酵解相关的能量代谢变化。采用免疫荧光和western blot检测神经炎症。结果6月龄APP/PS1小鼠睡眠时间缩短,认知功能受损。XX-F显著延长睡眠时间和恢复认知。此外,XX-F减少了淀粉样蛋白-β (Aβ)斑块的数量,改善了神经炎症,并通过降低丙酮酸激酶M2 (PKM2)和乳酸水平来抑制糖酵解,同时挽救了三磷酸腺苷(ATP)缺乏。结论XX-F可通过调节能量代谢和减少神经炎症来改善AD小鼠的睡眠和认知。这是一种潜在的治疗阿尔茨海默病的方法,需要进一步深入研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel traditional Chinese medicine formula restores sleep and cognitive function in APP/PS1 mice by targeting glycolytic pathways and neuroinflammatory responses.

BackgroundAlzheimer's disease (AD) is recognized as a multifactorial neurodegenerative disorder involving numerous cellular and molecular processes, such as sleep disturbance, imbalance in brain glucose metabolism and neuroinflammation; these dysregulations typically precede the onset of symptoms. Hence, the results of mono-target therapy after AD diagnosis are in many cases unsatisfactory.ObjectiveTraditional Chinese medicine (TCM) presents significant potential for treating AD. Sleep disorders are one of the early symptoms of AD; however, there is no effective solution to sleep disorders caused by AD. Some TCMs have been shown to treat sleep disorders by regulating energy metabolism or improving neuroinflammation. This study aims to investigate if XX-F administrated in advance could alleviate AD by improving sleep quality and neuroinflammation.MethodsMice were given Xiexintongfu formula (XX-F) intragastrically for three months. Morris water maze and pentobarbital-induced sleep test were performed to evaluate cognition and sleep. Determine changes in energy metabolism related to glycolysis through western blot and specific assay kits. Using immunofluorescence and western blot to detect neuroinflammation.ResultsShortened sleep duration and cognitive impairment were observed in 6-month-old APP/PS1 mice. XX-F significantly prolonged sleep duration and rescued cognition. In addition, XX-F reduced the number of amyloid-β (Aβ) plaques and ameliorated neuroinflammation, and inhibited glycolysis by reducing pyruvate kinase M2 (PKM2) and lactate levels while rescuing adenosine triphosphate (ATP) deficiency.ConclusionsWe demonstrate that XX-F can improve sleep and cognition of AD mice by regulating energy metabolism and reducing neuroinflammation. This is a potential treatment method for AD and requires further in-depth research.

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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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