慢性应激通过上调α-突触核蛋白诱导抑郁样行为和帕金森病

IF 6.7 1区 医学 Q1 NEUROSCIENCES
Danhao Xia, Min Xiong, Yingxu Yang, Xin Wang, Qiang Chen, Sheng Li, Lanxia Meng, Zhentao Zhang
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引用次数: 0

摘要

帕金森病(PD)是一种以α-突触核蛋白(α-syn)聚集和黑质纹状体多巴胺能神经元变性为特征的神经退行性疾病。抑郁是PD患者最常见的非运动症状之一。然而,PD与抑郁症之间的致病关系尚不清楚。在此,我们报道慢性应激可上调小鼠大脑中α-syn的表达。海马中α-syn的过表达复制了抑郁样表型,而α-syn的基因缺失增强了对慢性应激的抵抗力。此外,在过表达人A53T突变体α-syn的转基因小鼠模型(A53T小鼠)中,早期慢性应激促进α-syn聚集体的沉积。慢性应激也加重了A53T小鼠的多巴胺能变性和运动损伤。引人注目的是,α-syn包体也在一些遭受慢性应激的非转基因老年小鼠的大脑中被观察到。总之,我们的研究结果表明,慢性应激上调α-突触核蛋白的表达,导致抑郁样行为和帕金森病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chronic stress induces depression-like behaviors and Parkinsonism via upregulating α-synuclein

Chronic stress induces depression-like behaviors and Parkinsonism via upregulating α-synuclein

Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the aggregation of α-synuclein (α-syn) and the nigrostriatal dopaminergic neuronal degeneration. Depression is one of the most common non-motor symptoms of PD patients. However, the pathogenic connection between PD and depression is not well understood. Herein, we report that chronic stress upregulates the expression of α-syn in the mouse brain. Overexpression of α-syn in the hippocampus replicates depressive-like phenotypes, whereas the genetic deletion of α-syn enhances resistance to chronic stress. Furthermore, chronic stress in early life promoted the deposition of α-syn aggregates in a transgenic mouse model that overexpresses human A53T mutant α-syn (A53T mice). Chronic stress also exacerbated dopaminergic degeneration and motor impairments in A53T mice. Strikingly, α-syn inclusions were also observed in the brains of some aged non-transgenic mice subjected to chronic stress. Together, our findings suggest that chronic stress upregulates α-synuclein expression, resulting in depression-like behaviors and parkinsonism.

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来源期刊
NPJ Parkinson's Disease
NPJ Parkinson's Disease Medicine-Neurology (clinical)
CiteScore
9.80
自引率
5.70%
发文量
156
审稿时长
11 weeks
期刊介绍: npj Parkinson's Disease is a comprehensive open access journal that covers a wide range of research areas related to Parkinson's disease. It publishes original studies in basic science, translational research, and clinical investigations. The journal is dedicated to advancing our understanding of Parkinson's disease by exploring various aspects such as anatomy, etiology, genetics, cellular and molecular physiology, neurophysiology, epidemiology, and therapeutic development. By providing free and immediate access to the scientific and Parkinson's disease community, npj Parkinson's Disease promotes collaboration and knowledge sharing among researchers and healthcare professionals.
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