Department of Anatomy, Research Group for Mood Disorders, Medical School, University of Pécs, Szigeti út 12., 7624, Pecs, Hungary.
Centre for Neuroscience, University of Pécs, 7624, Pecs, Hungary.
J Neuroinflammation. 2022 Feb 2;19(1):31. doi: 10.1186/s12974-022-02399-w.
The neuropathological background of major depression and anxiety as non-motor symptoms of Parkinson's disease is much less understood than classical motor symptoms. Although, neurodegeneration of the Edinger-Westphal nucleus in human Parkinson's disease is a known phenomenon, its possible significance in mood status has never been elucidated. In this work we aimed at investigating whether neuron loss and alpha-synuclein accumulation in the urocortin 1 containing (UCN1) cells of the centrally-projecting Edinger-Westphal (EWcp) nucleus is associated with anxiety and depression-like state in the rat.
Systemic chronic rotenone administration as well as targeted leptin-saporin-induced lesions of EWcp/UCN1 neurons were conducted. Rotarod, open field and sucrose preference tests were performed to assess motor performance and mood status. Multiple immunofluorescence combined with RNAscope were used to reveal the functional-morphological changes. Two-sample Student's t test, Spearman's rank correlation analysis and Mann-Whitney U tests were used for statistics.
In the rotenone model, besides motor deficit, an anxious and depression-like phenotype was detected. Well-comparable neuron loss, cytoplasmic alpha-synuclein accumulation as well as astro- and microglial activation were observed both in the substantia nigra pars compacta and EWcp. Occasionally, UCN1-immunoreactive neuronal debris was observed in phagocytotic microglia. UCN1 peptide content of viable EWcp cells correlated with dopaminergic substantia nigra cell count. Importantly, other mood status-related dopaminergic (ventral tegmental area), serotonergic (dorsal and median raphe) and noradrenergic (locus ceruleus and A5 area) brainstem centers did not show remarkable morphological changes. Targeted partial selective EWcp/UCN1 neuron ablation induced similar mood status without motor symptoms.
Our findings collectively suggest that neurodegeneration of urocortinergic EWcp contributes to the mood-related non-motor symptoms in toxic models of Parkinson's disease in the rat.
帕金森病的非运动症状,如重度抑郁症和焦虑症,其神经病理学基础的了解远不如经典运动症状。尽管人类帕金森病中 Edinger-Westphal 核的神经退行性变是已知的现象,但它在情绪状态中的可能意义从未被阐明。在这项工作中,我们旨在研究中枢投射的 Edinger-Westphal(EWcp)核中含有urocortin 1(UCN1)的细胞的神经元丢失和 alpha-synuclein 积累是否与大鼠的焦虑和抑郁状态有关。
进行了系统性慢性鱼藤酮给药以及靶向瘦素-saporin 诱导的 EWcp/UCN1 神经元损伤。旋转棒、旷场和蔗糖偏好测试用于评估运动表现和情绪状态。采用多重免疫荧光结合 RNAscope 揭示功能形态变化。采用两样本学生 t 检验、Spearman 秩相关分析和 Mann-Whitney U 检验进行统计学分析。
在鱼藤酮模型中,除了运动缺陷外,还检测到焦虑和抑郁样表型。在黑质致密部和 EWcp 中均观察到相似的神经元丢失、细胞质 alpha-synuclein 积累以及星形胶质细胞和小胶质细胞激活。偶尔,吞噬性小胶质细胞中可见 UCN1 免疫反应性神经元碎片。存活的 EWcp 细胞中的 UCN1 肽含量与黑质多巴胺能细胞计数相关。重要的是,其他与情绪状态相关的多巴胺能(腹侧被盖区)、5-羟色胺能(背侧和中缝核)和去甲肾上腺素能(蓝斑和 A5 区)脑干中枢没有明显的形态变化。靶向选择性 EWcp/UCN1 神经元消融诱导了类似的情绪状态而没有运动症状。
我们的研究结果表明,urocortinergic EWcp 的神经退行性变与大鼠帕金森病的毒性模型中的情绪相关的非运动症状有关。