Neuroprotection Against Parkinson's Disease Through the Activation of Akt/GSK3β Signaling Pathway by Tovophyllin A

被引:15
作者
Huang, Yanjun [1 ]
Sun, Lirong [1 ]
Zhu, Shuzhen [2 ]
Xu, Liu [1 ]
Liu, Shuhu [1 ]
Yuan, Chunhua [1 ]
Guo, Yanwu [3 ]
Wang, Xuemin [1 ]
机构
[1] Southern Med Univ, Guangdong Hong Kong Macao Greater Bay Area Ctr Br, Sch Basic Med Sci, Key Lab Mental Hlth,Minist Educ,Dept Neurobiol,Sc, Guangzhou, Peoples R China
[2] Southern Med Univ, Zhujiang Hosp, Dept Neurol, Guangzhou, Peoples R China
[3] Southern Med Univ, Zhujiang Hosp, Dept Neurosurg, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Tovophyllin A; Parkinson's disease; apoptosis; Akt; GSK3; beta; GLYCOGEN-SYNTHASE KINASE-3; GARCINIA-MANGOSTANA L; INDUCED NEUROTOXICITY; MOUSE MODEL; MEDICINAL PROPERTIES; SH-SY5Y CELLS; INHIBITION; XANTHONES; APOPTOSIS; PROTECTS;
D O I
10.3389/fnins.2020.00723
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Parkinson's disease (PD) is one of the most prevalent and life-threatening neurodegenerative disease and mainly characterized by lack of sufficient dopaminergic neurons in the substantia nigra pars compacta (SNc). Although current treatments help to alleviate clinical symptoms, effective therapies preventing neuronal loss remain scarce. Tovophyllin A (TA), one of the xanthones extracted fromGarcinia mangostanaL. (GM), has recently been reported to play a beneficial role in the therapy of neurodegenerative diseases. In our research, we explored whether TA has protective effects on dopaminergic neurons in PD models. We found that TA significantly reduced apoptotic cell death in primary cortical neurons treated with 1-methyl-4-phenyl pyridinium (MPP+) or paraquat (PQ) in thein vitroPD model. In anin vivoacute PD model induced by 1-methyl4-phenyl-1,2,3,5-tetrahydropyridine (MPTP) treatment, TA also attenuated the resulting behavioral dysfunctions and dopaminergic neuron loss. In the collected brain tissues, TA increased the phosphorylation of Akt and GSK-3 beta, which may be related to TA-mediated dopaminergic neuronal protective effects. In summary, our results illustrated that TA is a powerful cytoprotective agent for dopaminergic neurons in the MPTP-induced PD model, suggesting TA as a possible therapeutic candidate for PD.
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页数:10
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