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首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >Dysregulation of stress systems and nitric oxide signaling underlies neuronal dysfunction in Alzheimer's disease
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Dysregulation of stress systems and nitric oxide signaling underlies neuronal dysfunction in Alzheimer's disease

机译:应力系统的失调和一氧化氮信号底层患有阿尔茨海默病的神经元功能障碍

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摘要

Stress is a multimodal response involving the coordination of numerous body systems in order to maximize the chance of survival. However, long term activation of the stress response results in neuronal oxidative stress via reactive oxygen and nitrogen species generation, contributing to the development of depression. Stress-induced depression shares a high comorbidity with other neurological conditions including Alzheimer's disease (AD) and dementia, often appearing as one of the earliest observable symptoms in these diseases. Furthermore, stress and/or depression appear to exacerbate cognitive impairment in the context of AD associated with dysfunctional catecholaminergic signaling. Given there are a number of homologous pathways involved in the pathophysiology of depression and AD, this article will highlight the mechanisms by which stress-induced perturbations in oxidative stress, and particularly NO signaling, contribute to neurodegeneration.
机译:压力是一种涉及许多体系的协调的多模态反应,以最大化存活的机会。 然而,长期激活应力反应导致通过反应性氧和氮物质产生的神经元氧化应激,有助于抑郁的发育。 应激诱发的抑郁症与其他神经系统疾病共享高合并症,包括阿尔茨海默病(Ad)和痴呆,通常作为这些疾病中最早的可观察症状之一。 此外,应激和/或抑郁症在与功能失调的儿茶酚胺能信号传导相关的广告中加剧认知障碍。 鉴于抑郁症和广告的病理生理学涉及许多同源途径,本文将突出氧化应激的应激扰动,特别是无信号传导的机制,有助于神经变性。

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