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在MPTP诱导的帕金森病体内模型中,槲皮素通过激活PI3K/Akt/GSK-3β信号通路来保护神经元免受毒性作用。

Quercetin protects against neuronal toxicity by activating the PI3K/Akt/GSK-3β pathway in vivo models of MPTP-induced Parkinson's disease.

作者信息

Li Yajuan, Man Minghao, Tian Yiyuan, Zhao Gang, Liu FengZhou, Zhao JingYu, Huang Songya, Xue Junhui, Chang Wei

机构信息

Center for Aerospace Clinical Medicine, Department of Aerospace Medicine, Air Force Medical University, Xi'an, 710032, China.

Department of Neurosurgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710038, Shaanxi, China.

出版信息

Inflammopharmacology. 2025 Mar 27. doi: 10.1007/s10787-025-01712-2.

Abstract

BACKGROUND

Quercetin is a flavonoid commonly found in various fruits, vegetables, and grains. Studies have demonstrated that quercetin may help protect neuronal cells from damage caused by neurotoxins associated with Parkinson's disease, however, the underlying mechanism remains unclear.

AIM

The current study aimed to investigate the neuroprotective effects of quercetin in MPTP-induced Parkinson's disease mouse models and elucidate its mechanistic role in modulating the PI3K/Akt/GSK-3β signaling pathway.

MATERIALS AND METHODS

Male C57BL/6 mice were divided into control, MPTP, quercetin, and MPTP + quercetin groups. The protective effects of quercetin on Parkinson's disease in mice were evaluated using animal behaviour analysis, histopathological examination, and immunofluorescence staining. Subsequently, network pharmacology was utilized to determine the primary target sites of quercetin in Parkinson's disease. Finally, western blotting and molecular docking techniques were applied to validate the identified targets.

RESULTS

Quercetin significantly improved motor deficits in MPTP mice, reduced neuronal atrophy, and preserved TH dopaminergic neurons. Western blotting analysis revealed quercetin upregulated anti-inflammatory IL-10 (p < 0.01) and TGF-β (p < 0.01) while suppressing pro-inflammatory IL-1β (p < 0.01) and iNOS (p < 0.01). It activated the PI3K/Akt/GSK-3β pathway by increasing phosphorylation of PI3K (p < 0.01), Akt (p < 0.01), and GSK-3β (p < 0.01). Quercetin also elevated anti-apoptotic Bcl-2 (p < 0.01) and reduced pro-apoptotic Bax (p < 0.01) and Caspase-9 (p < 0.01). Molecular docking confirmed strong binding between quercetin and PI3K/Akt/GSK-3β (binding energies: -6.44 to -5.24 kcal/mol).

CONCLUSION

Quercetin alleviates Parkinson's disease pathology by inhibiting neuroinflammation, reducing apoptosis, and activating the PI3K/Akt/GSK-3β pathway. These findings underscore its potential as a multi-target therapeutic agent for Parkinson's disease.

摘要

背景

槲皮素是一种常见于各种水果、蔬菜和谷物中的类黄酮。研究表明,槲皮素可能有助于保护神经元细胞免受与帕金森病相关的神经毒素的损害,然而,其潜在机制仍不清楚。

目的

本研究旨在探讨槲皮素在MPTP诱导的帕金森病小鼠模型中的神经保护作用,并阐明其在调节PI3K/Akt/GSK-3β信号通路中的作用机制。

材料与方法

将雄性C57BL/6小鼠分为对照组、MPTP组、槲皮素组和MPTP +槲皮素组。通过动物行为分析、组织病理学检查和免疫荧光染色评估槲皮素对小鼠帕金森病的保护作用。随后,利用网络药理学确定槲皮素在帕金森病中的主要靶点。最后,应用蛋白质免疫印迹法和分子对接技术验证所确定的靶点。

结果

槲皮素显著改善了MPTP小鼠的运动功能障碍,减少了神经元萎缩,并保留了TH多巴胺能神经元。蛋白质免疫印迹分析显示,槲皮素上调抗炎性细胞因子IL-10(p < 0.01)和TGF-β(p < 0.01),同时抑制促炎性细胞因子IL-1β(p < 0.01)和iNOS(p < 0.01)。它通过增加PI3K(p < 0.01)、Akt(p < 0.01)和GSK-3β(p < 0.01)的磷酸化来激活PI3K/Akt/GSK-3β信号通路。槲皮素还上调抗凋亡蛋白Bcl-2(p < 0.01),并降低促凋亡蛋白Bax(p < 0.01)和Caspase-9(p < 0.01)的表达。分子对接证实槲皮素与PI3K/Akt/GSK-3β之间有强结合(结合能:-6.44至-5.24千卡/摩尔)。

结论

槲皮素通过抑制神经炎症、减少细胞凋亡和激活PI3K/Akt/GSK-3β信号通路来减轻帕金森病的病理变化。这些发现突出了其作为帕金森病多靶点治疗药物的潜力。

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