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大蒜衍生的蒜素通过激活PKA/p-CREB/BDNF/DAT通路和抑制凋亡来减轻帕金森病。

Garlic-Derived Allicin Attenuates Parkinson's Disease via PKA/p-CREB/BDNF/DAT Pathway Activation and Apoptotic Inhibition.

作者信息

Zeng Wanchen, Wang Yingkai, Liu Yang, Liu Xiaomin, Qi Zhongquan

机构信息

School of Medicine, Guangxi University, Nanning 530004, China.

出版信息

Molecules. 2025 Aug 4;30(15):3265. doi: 10.3390/molecules30153265.

Abstract

Allicin (ALC), a naturally occurring organosulfur compound derived from garlic (), exhibits potential neuroprotective properties. Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by degeneration of dopaminergic neurons and motor dysfunction. This study utilized bioinformatics and network pharmacology methods to predict the anti-PD mechanism of ALC and established in vivo and in vitro PD models using 6-hydroxydopamine (6-OHDA) for experimental verification. Network pharmacological analysis indicates that apoptosis regulation and the PKA/p-CREB/BDNF signaling pathway are closely related to the anti-PD effect of ALC, and protein kinase A (PKA) and dopamine transporter (DAT) are key molecular targets. The experimental results show that ALC administration can alleviate the cytotoxicity of SH-SY5Y induced by 6-OHDA and simultaneously improve the motor dysfunction and dopaminergic neuron loss in PD mice. In addition, ALC can also activate the PKA/p-CREB/BDNF signaling pathway and increase the DAT level in brain tissue, regulate the expression of BAX and Bcl-2, and reduce neuronal apoptosis. These results indicate that ALC can exert anti-PD effects by up-regulating the PKA/p-CREB/BDNF/DAT signaling pathway and inhibiting neuronal apoptosis, providing theoretical support for the application of ALC in PD.

摘要

大蒜素(ALC)是一种源自大蒜的天然有机硫化合物,具有潜在的神经保护特性。帕金森病(PD)是一种进行性神经退行性疾病,其特征是多巴胺能神经元变性和运动功能障碍。本研究利用生物信息学和网络药理学方法预测ALC的抗PD机制,并使用6-羟基多巴胺(6-OHDA)建立体内和体外PD模型进行实验验证。网络药理学分析表明,细胞凋亡调控和PKA/p-CREB/BDNF信号通路与ALC的抗PD作用密切相关,蛋白激酶A(PKA)和多巴胺转运体(DAT)是关键分子靶点。实验结果表明,给予ALC可减轻6-OHDA诱导的SH-SY5Y细胞毒性,同时改善PD小鼠的运动功能障碍和多巴胺能神经元丢失。此外,ALC还可激活PKA/p-CREB/BDNF信号通路,提高脑组织中DAT水平,调节BAX和Bcl-2的表达,减少神经元凋亡。这些结果表明,ALC可通过上调PKA/p-CREB/BDNF/DAT信号通路和抑制神经元凋亡发挥抗PD作用,为ALC在PD中的应用提供了理论支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ad5/12348316/de9905284f28/molecules-30-03265-g001.jpg

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