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(萝芙木)普雷恩精油在阿尔茨海默病中的治疗潜力:体内脑电图信号分析、体外SH-SY5Y细胞模型及网络药理学

The Therapeutic Potential of (Lour.) Prain Essential Oil in Alzheimer's Disease: EEG Signal Analysis In Vivo, SH-SY5Y Cell Model In Vitro, and Network Pharmacology.

作者信息

Qin Sheng, Fang Jiayi, He Xin, Yu Genfa, Yi Fengping, Zhu Guangyong

机构信息

Department of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, China.

出版信息

Biology (Basel). 2024 Jul 18;13(7):544. doi: 10.3390/biology13070544.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder that is projected by the WHO to affect over 100 million people by 2050. Clinically, AD patients undergoing long-term antipsychotic treatment often experience severe anxiety or depression in later stages. Furthermore, early-stage AD manifests with weakened α waves in the brain, progressing to diminished α and β waves in late-stage disease, reflecting changes in emotional states and disease progression. In this study, EEG signal analysis revealed that inhalation of (Lour.) Prain essential oil (DPEO) enhanced δ, θ, α and β wave powers in the frontal and parietal lobes, with a rising trend in the β/α ratio in the temporal lobe. These findings suggest an alleviation of anxiety and an enhancement of cognitive functions. Treatment of the AD SH-SY5Y (human neuroblastoma cells) cell model with DPEO resulted in decreased intracellular levels of Aβ, GSK-3β, P-Tau, IL-1β, TNF-α, IL-6, COX-2, OFR, and HFR, alongside reduced AchE and BchE activities and increased SOD activity. Network pharmacology analysis indicated a potential pharmacological mechanism involving the JAK-STAT pathway. Our study provides evidence supporting DPEO's role in modulating anxiety and slowing AD pathological progression.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,世界卫生组织预计到2050年将有超过1亿人受其影响。临床上,接受长期抗精神病药物治疗的AD患者在后期常出现严重焦虑或抑郁。此外,AD早期表现为大脑α波减弱,疾病后期α波和β波均减少,这反映了情绪状态和疾病进展的变化。在本研究中,脑电图信号分析显示,吸入(罗勒)普雷恩精油(DPEO)可增强额叶和顶叶的δ波、θ波、α波和β波功率,颞叶β/α比值呈上升趋势。这些发现表明焦虑得到缓解,认知功能得到增强。用DPEO处理AD SH-SY5Y(人神经母细胞瘤细胞)细胞模型,导致细胞内Aβ、GSK-3β、P-Tau、IL-1β、TNF-α、IL-6、COX-2、OFR和HFR水平降低,同时AchE和BchE活性降低,SOD活性增加。网络药理学分析表明其潜在药理机制涉及JAK-STAT通路。我们的研究为DPEO在调节焦虑和减缓AD病理进展中的作用提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be35/11274073/f743371acab6/biology-13-00544-g001.jpg

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