散发性阿尔茨海默病早期慢性应激诱发蓝斑改变。

Donné Minné, Jeanine L Marnewick, Penelope Engel-Hills
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引用次数: 0

摘要

由于慢性压力的生物学机制与阿尔茨海默病的病理生理学之间的相似性,在阿尔茨海默病(AD)的一生中长期暴露于压力一直是许多研究的焦点。事实上,与该疾病相关的最早异常是蓝斑神经元中存在磷酸化的tau蛋白,对压力和感知到的威胁有高度反应的大脑结构。在这里,我们介绍了一个有用的概念来理解AD退行性过程中涉及的许多复杂的、相互作用的神经病理学变化。作为对慢性应激的反应,在症状出现前几十年开始在蓝斑内积累的异常tau蛋白似乎是AD级联反应中的主要病理事件,引发了一系列相互作用的大脑变化,包括神经元兴奋性毒性、内分泌改变、炎症、氧化应激和淀粉样蛋白斑块恶化。虽然人们承认,压力不一定是所有情况下的主要诱因,但早期tau诱导的蓝斑-去甲肾上腺素途径的变化表明,可能存在一个治疗窗口,可以采取预防措施来管理压力并恢复HPA轴内的平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early Chronic Stress Induced Changes within the Locus Coeruleus in Sporadic Alzheimer's Disease.

Chronic exposure to stress throughout the lifespan has been the focus of many studies on Alzheimer's disease (AD) because of the similarities between the biological mechanisms involved in chronic stress and the pathophysiology of AD. In fact, the earliest abnormality associated with the disease is the presence of phosphorylated tau protein in locus coeruleus neurons, a brain structure highly responsive to stress and perceived threat. Here, we introduce allostatic load as a useful concept for understanding many of the complex, interacting neuropathological changes involved in the AD degenerative process. In response to chronic stress, aberrant tau proteins that begin to accumulate within the locus coeruleus decades prior to symptom onset appear to represent a primary pathological event in the AD cascade, triggering a wide range of interacting brain changes involving neuronal excitotoxicity, endocrine alterations, inflammation, oxidative stress, and amyloid plaque exacerbation. While it is acknowledged that stress will not necessarily be the major precipitating factor in all cases, early tau-induced changes within the locus coeruleus-norepinephrine pathway suggests that a therapeutic window might exist for preventative measures aimed at managing stress and restoring balance within the HPA axis.

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