Huang Yanjun, Sun Lirong, Zhu Shuzhen, Xu Liu, Liu Shuhu, Yuan Chunhua, Guo Yanwu, Wang Xuemin
Key Laboratory of Mental Health of the Ministry of Education, Guangdong-Hong Kong-Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence, Guangdong Province Key Laboratory of Psychiatric Disorders, Department of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Department of Neurology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Front Neurosci. 2020 Jul 9;14:723. doi: 10.3389/fnins.2020.00723. eCollection 2020.
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 from L. (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 the PD model. In an acute 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-3β, 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.
帕金森病(PD)是最常见且危及生命的神经退行性疾病之一,主要特征是黑质致密部(SNc)中多巴胺能神经元不足。尽管目前的治疗有助于缓解临床症状,但预防神经元丢失的有效疗法仍然匮乏。托沃菲林A(TA)是从L.(GM)中提取的一种氧杂蒽酮,最近有报道称其在神经退行性疾病治疗中发挥有益作用。在我们的研究中,我们探讨了TA对PD模型中多巴胺能神经元是否具有保护作用。我们发现,TA显著减少了在PD模型中用1-甲基-4-苯基吡啶鎓(MPP)或百草枯(PQ)处理的原代皮质神经元中的凋亡细胞死亡。在由1-甲基-4-苯基-1,2,3,5-四氢吡啶(MPTP)处理诱导的急性PD模型中,TA也减轻了由此产生的行为功能障碍和多巴胺能神经元丢失。在收集的脑组织中,TA增加了Akt和GSK-3β的磷酸化,这可能与TA介导的多巴胺能神经元保护作用有关。总之,我们的结果表明,TA是MPTP诱导的PD模型中多巴胺能神经元的一种强大的细胞保护剂,表明TA可能是PD的一种治疗候选药物。