School of Biomedical Sciences and Pharmacy and the Priority Research Centre for Stroke and Brain Injury, University of Newcastle, Callaghan, NSW, Australia; Hunter Medical Research Institute, Newcastle, NSW, Australia; NHMRC Centre of Research Excellence Stroke Rehabilitation and Brain Recovery, Heidelberg, VIC, Australia.
School of Biomedical Sciences and Pharmacy and the Priority Research Centre for Stroke and Brain Injury, University of Newcastle, Callaghan, NSW, Australia; Hunter Medical Research Institute, Newcastle, NSW, Australia.
Brain Behav Immun. 2017 Feb;60:117-125. doi: 10.1016/j.bbi.2016.10.001. Epub 2016 Oct 4.
Exposure to psychological stress is known to seriously disrupt the operation of the substantia nigra (SN) and may in fact initiate the loss of dopaminergic neurons within the SN. In this study, we aimed to investigate how chronic stress modified the SN in adult male mice. Using a paradigm of repeated restraint stress (an average of 20h per week for 6weeks), we examined changes within the SN using western blotting and immunohistochemistry. We demonstrated that chronic stress was associated with a clear loss of dopaminergic neurons within the SN. The loss of dopaminergic neurons was accompanied by higher levels of oxidative stress damage, indexed by levels of protein carbonylation and strong suppression of both microglial and astrocytic responses. In addition, we demonstrated for the first time, that chronic stress alone enhanced the aggregation of α-synuclein into the insoluble protein fraction. These results indicate that chronic stress triggered loss of dopaminergic neurons by increasing oxidative stress, suppressing glial neuroprotective functions and enhancing the aggregation of the neurotoxic protein, α-synuclein. Collectively, these results reinforce the negative effects of chronic stress on the viability of dopaminergic cells within the SN.
暴露于心理压力会严重扰乱黑质(SN)的运作,实际上可能会引发 SN 内多巴胺能神经元的丧失。在这项研究中,我们旨在研究慢性应激如何改变成年雄性小鼠的 SN。我们使用重复束缚应激范式(每周平均 20 小时,持续 6 周),通过 Western blot 和免疫组织化学方法检查 SN 内的变化。我们表明,慢性应激与 SN 内多巴胺能神经元的明显丧失有关。多巴胺能神经元的丧失伴随着氧化应激损伤水平的升高,其指标为蛋白质羰基化水平的升高以及小胶质细胞和星形胶质细胞反应的强烈抑制。此外,我们首次证明,慢性应激本身会增强α-突触核蛋白聚集成不溶性蛋白部分。这些结果表明,慢性应激通过增加氧化应激、抑制神经胶质的神经保护功能以及增强神经毒性蛋白α-突触核蛋白的聚集,引发多巴胺能神经元的丧失。总的来说,这些结果强化了慢性应激对 SN 内多巴胺能细胞活力的负面影响。