Yang Changwei, Zhang Tingting, Wang Wuqiong, Xiang Yilan, Huang Qun, Xie Chenglong, Zhao Liangcai, Zheng Hong, Yang Yunjun, Gao Hongchang
School of Pharmaceutical Science, Wenzhou Medical University, Wenzhou, China.
Department of Radiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Front Aging Neurosci. 2020 Mar 17;12:75. doi: 10.3389/fnagi.2020.00075. eCollection 2020.
Several lines of evidence point to alteration in brain metabolic homeostasis in Parkinson's disease (PD) and levodopa-induced dyskinesia (LID), yet the metabolic mechanism in different brain regions underlying PD and LID remains largely unknown. The present study aimed to uncover the metabolic pathways across anatomical regions in the brain of PD and LID. Using an NMR-based metabolomic approach, we generated the metabolomics profiling data from six different brain regions of PD rats and following the onset of LIDs. The diversity of metabolite patterns across the brain and its relation to PD and LID were further investigated through principal component analysis (PCA) and multivariate general linear model. Compared with control rats, dopamine loss in PD rats produced a marked and persistent metabolic disturbance in neurotransmitter metabolism and energy pathway, resulting in a metabolic imbalance among different brain regions. In LID rats, levodopa replacement did not restore the midbrain-striatum metabolic crosstalk and metabolic disturbance throughout the brain was involved in levodopa related involuntary movements. Most notably, the midbrain and right cortex were identified as the primary regions of metabolic abnormalities in PD and LID rats. Neurochemical differences in metabolic phenotypes were mainly defined by various neurotransmitters including glutamate, glutamine and aspartate. Accordingly, we found that the PD and LID rats exhibited lower levels of synaptophysin (SYP), a marker for synaptic plasticity, compared with control rats. These findings provide key insights into the metabolic mechanism underlying PD and LID by defining brain-region specific metabolic phenotype, with implications for developing targeted therapies.
多条证据表明帕金森病(PD)和左旋多巴诱导的异动症(LID)存在脑代谢稳态改变,但PD和LID不同脑区的代谢机制仍 largely未知。本研究旨在揭示PD和LID大鼠脑内不同解剖区域的代谢途径。采用基于核磁共振的代谢组学方法,我们从PD大鼠的六个不同脑区以及LID发作后生成了代谢组学图谱数据。通过主成分分析(PCA)和多元通用线性模型进一步研究了全脑代谢物模式的多样性及其与PD和LID的关系。与对照大鼠相比,PD大鼠多巴胺缺失在神经递质代谢和能量途径中产生了明显且持续的代谢紊乱,导致不同脑区之间的代谢失衡。在LID大鼠中,左旋多巴替代并未恢复中脑 - 纹状体代谢串扰,且全脑的代谢紊乱与左旋多巴相关的不自主运动有关。最值得注意的是,中脑和右侧皮层被确定为PD和LID大鼠代谢异常的主要区域。代谢表型的神经化学差异主要由包括谷氨酸、谷氨酰胺和天冬氨酸在内的各种神经递质定义。因此,我们发现与对照大鼠相比,PD和LID大鼠的突触素(SYP)水平较低,突触素是突触可塑性的标志物。这些发现通过定义脑区特异性代谢表型,为PD和LID潜在的代谢机制提供了关键见解,对开发靶向治疗具有重要意义。