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调节觉醒以克服帕金森病的步态障碍:去甲肾上腺素能系统如何成为一把双刃剑。

Modulating arousal to overcome gait impairments in Parkinson's disease: how the noradrenergic system may act as a double-edged sword.

作者信息

Tosserams Anouk, Bloem Bastiaan R, Ehgoetz Martens Kaylena A, Helmich Rick C, Kessels Roy P C, Shine James M, Taylor Natasha L, Wainstein Gabriel, Lewis Simon J G, Nonnekes Jorik

机构信息

Department of Neurology, Center of Expertise for Parkinson and Movement Disorders, Radboud University Medical Centre, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.

Department of Rehabilitation, Center of Expertise for Parkinson and Movement Disorders, Radboud University Medical Centre, Donders Institute for Brain, Cognition and Behaviour, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.

出版信息

Transl Neurodegener. 2023 Mar 26;12(1):15. doi: 10.1186/s40035-023-00347-z.

Abstract

In stressful or anxiety-provoking situations, most people with Parkinson's disease (PD) experience a general worsening of motor symptoms, including their gait impairments. However, a proportion of patients actually report benefits from experiencing-or even purposely inducing-stressful or high-arousal situations. Using data from a large-scale international survey study among 4324 people with PD and gait impairments within the online Fox Insight (USA) and ParkinsonNEXT (NL) cohorts, we demonstrate that individuals with PD deploy an array of mental state alteration strategies to cope with their gait impairment. Crucially, these strategies differ along an axis of arousal-some act to heighten, whereas others diminish, overall sympathetic tone. Together, our observations suggest that arousal may act as a double-edged sword for gait control in PD. We propose a theoretical, neurobiological framework to explain why heightened arousal can have detrimental effects on the occurrence and severity of gait impairments in some individuals, while alleviating them in others. Specifically, we postulate that this seemingly contradictory phenomenon is explained by the inherent features of the ascending arousal system: namely, that arousal is related to task performance by an inverted u-shaped curve (the so-called Yerkes and Dodson relationship). We propose that the noradrenergic locus coeruleus plays an important role in modulating PD symptom severity and expression, by regulating arousal and by mediating network-level functional integration across the brain. The ability of the locus coeruleus to facilitate dynamic 'cross-talk' between distinct, otherwise largely segregated brain regions may facilitate the necessary cerebral compensation for gait impairments in PD. In the presence of suboptimal arousal, compensatory networks may be too segregated to allow for adequate compensation. Conversely, with supraoptimal arousal, increased cross-talk between competing inputs of these complementary networks may emerge and become dysfunctional. Because the locus coeruleus degenerates with disease progression, finetuning of this delicate balance becomes increasingly difficult, heightening the need for mental strategies to self-modulate arousal and facilitate shifting from a sub- or supraoptimal state of arousal to improve gait performance. Recognition of this underlying mechanism emphasises the importance of PD-specific rehabilitation strategies to alleviate gait disability.

摘要

在压力大或引发焦虑的情况下,大多数帕金森病(PD)患者会出现运动症状普遍恶化的情况,包括步态障碍。然而,有一部分患者实际上报告称,经历——甚至故意诱发——压力大或高度兴奋的情况会带来益处。我们利用在线福克斯洞察(美国)和帕金森病下一步(荷兰)队列中4324名患有PD和步态障碍的人群的大规模国际调查研究数据,证明了PD患者会采用一系列心理状态改变策略来应对步态障碍。至关重要的是,这些策略在唤醒轴上存在差异——一些策略会增强,而另一些则会降低整体交感神经张力。我们的观察结果共同表明,唤醒可能是PD步态控制的一把双刃剑。我们提出了一个理论性的神经生物学框架,以解释为什么高度唤醒在一些个体中会对步态障碍的发生和严重程度产生不利影响,而在另一些个体中却能减轻这些影响。具体而言,我们假设这种看似矛盾的现象可以通过上行唤醒系统的固有特征来解释:即唤醒与任务表现呈倒U形曲线关系(所谓的耶基斯和多德森关系)。我们提出,去甲肾上腺素能蓝斑在调节PD症状的严重程度和表现方面发挥着重要作用,它通过调节唤醒以及介导大脑各区域之间的网络水平功能整合来实现这一点。蓝斑促进不同的、原本在很大程度上相互隔离的脑区之间动态“相互作用”的能力,可能有助于为PD患者的步态障碍进行必要的大脑补偿。在唤醒不足的情况下,补偿网络可能过于隔离,无法进行充分补偿。相反,在唤醒过度的情况下,这些互补网络的竞争性输入之间可能会出现增加的相互作用并变得功能失调。由于蓝斑会随着疾病进展而退化,微调这种微妙的平衡变得越来越困难,这就增加了采用心理策略来自我调节唤醒并促进从次优或超优唤醒状态转变以改善步态表现的需求。认识到这一潜在机制强调了针对PD的康复策略对减轻步态残疾的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f4b/10040128/add76a9ae652/40035_2023_347_Fig1_HTML.jpg

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