Lu Yi, Zhang Xiaoxia, Zhao Liangcai, Yang Changwei, Pan Linlin, Li Chen, Liu Kun, Bai Guanghui, Gao Hongchang, Yan Zhihan
Department of Radiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Institute of Metabonomics & Medical NMR, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Front Neurosci. 2018 Feb 20;12:90. doi: 10.3389/fnins.2018.00090. eCollection 2018.
Metabolic confusion has been linked to the pathogenesis of Parkinson's disease (PD), while the dynamic changes associated with the onset and progression of PD remain unclear. Herein, dynamic changes in metabolites were detected from the initiation to the development of 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) -induced Parkinsonism model to elucidate its potential metabolic mechanism. H nuclear magnetic resonance (NMR) spectroscopy was used to measure metabolite changes in the striatum and substantia nigra (SN) of mice at 1, 7, and 21 days after injection of MPTP. Metabolomic analysis revealed a clear separation of the overall metabolites between PD and control mice at different time points. Glutamate (Glu) in the striatum was significantly elevated at induction PD day 1 mice, which persisted to day 21. N-acetylaspartate (NAA) increased in the striatum of induction PD mice on days 1 and 7, but no significant difference was found in striatum on day 21. Myo-Inositol (mI) and taurine (Tau) were also disturbed in the striatum in induction PD day 1 mice. Additionally, key enzymes in the glutamate-glutamine cycle were significantly increased in PD mice. These findings suggest that neuron loss and motor function impairment in induction PD mice may be linked to overactive glutamate-glutamine cycle and altered membrane metabolism.
代谢紊乱与帕金森病(PD)的发病机制有关,而与PD发病和进展相关的动态变化仍不清楚。在此,检测了1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病模型从发病到发展过程中代谢物的动态变化,以阐明其潜在的代谢机制。采用氢核磁共振(NMR)光谱法测量MPTP注射后1、7和21天小鼠纹状体和黑质(SN)中的代谢物变化。代谢组学分析显示,在不同时间点,PD小鼠和对照小鼠的总体代谢物有明显分离。诱导PD第1天小鼠纹状体中的谷氨酸(Glu)显著升高,并持续至第21天。诱导PD小鼠纹状体中的N-乙酰天门冬氨酸(NAA)在第1天和第7天增加,但在第21天纹状体中未发现显著差异。诱导PD第1天小鼠纹状体中的肌醇(mI)和牛磺酸(Tau)也受到干扰。此外,PD小鼠谷氨酸-谷氨酰胺循环中的关键酶显著增加。这些发现表明,诱导PD小鼠的神经元丢失和运动功能损害可能与谷氨酸-谷氨酰胺循环过度活跃和膜代谢改变有关。