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下船综合征:是环路的问题吗?

Mal de Debarquement Syndrome: A Matter of Loops?

作者信息

Mucci Viviana, Indovina Iole, Browne Cherylea J, Blanchini Franco, Giordano Giulia, Marinelli Lucio, Burlando Bruno

机构信息

School of Science, Western Sydney University, Penrith, NSW, Australia.

Laboratory of Neuromotor Physiology, Istituto di Ricovero e Cura a Carattere Scientifico Fondazione Santa Lucia, Rome, Italy.

出版信息

Front Neurol. 2020 Nov 10;11:576860. doi: 10.3389/fneur.2020.576860. eCollection 2020.

DOI:10.3389/fneur.2020.576860
PMID:33244308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7683778/
Abstract

Mal de Debarquement Syndrome (MdDS) is a poorly understood neurological disorder affecting mostly perimenopausal women. MdDS has been hypothesized to be a maladaptation of the vestibulo-ocular reflex, a neuroplasticity disorder, and a consequence of neurochemical imbalances and hormonal changes. Our hypothesis considers elements from these theories, but presents a novel approach based on the analysis of functional loops, according to Systems and Control Theory. MdDS is characterized by a persistent sensation of self-motion, usually occurring after sea travels. We assume the existence of a neuronal mechanism acting as an oscillator, i.e., an adaptive internal model, that may be able to cancel a sinusoidal disturbance of posture experienced aboard, due to wave motion. Thereafter, we identify this mechanism as a multi-loop neural network that spans between vestibular nuclei and the flocculonodular lobe of the cerebellum. We demonstrate that this loop system has a tendency to oscillate, which increases with increasing strength of neuronal connections. Therefore, we hypothesize that synaptic plasticity, specifically long-term potentiation, may play a role in making these oscillations poorly damped. Finally, we assume that the neuromodulator Calcitonin Gene-Related Peptide, which is modulated in perimenopausal women, exacerbates this process thus rendering the transition irreversible and consequently leading to MdDS. The concept of an oscillator that becomes noxiously permanent can be used as a model for MdDS, given a high correlation between patients with MdDS and sea travels involving undulating passive motion, and an alleviation of symptoms when patients are re-exposed to similar passive motion. The mechanism could be further investigated utilizing posturography tests to evaluate if subjective perception of motion matches with objective postural instability. Neurochemical imbalances that would render individuals more susceptible to developing MdDS could be investigated through hormonal profile screening. Alterations in the connections between vestibular nuclei and cerebellum, notably GABAergic fibers, could be explored by neuroimaging techniques as well as transcranial magnetic stimulation. If our hypothesis were tested and verified, optimal targets for MdDS treatment could be found within both the neural networks and biochemical factors that are deemed to play a fundamental role in loop functioning and synaptic plasticity.

摘要

下船综合征(MdDS)是一种了解甚少的神经系统疾病,主要影响围绝经期女性。有人提出假说,认为MdDS是前庭眼反射的适应不良、一种神经可塑性障碍,以及神经化学失衡和激素变化的结果。我们的假说综合了这些理论的要素,但根据系统与控制理论,提出了一种基于功能回路分析的新方法。MdDS的特征是存在持续的自我运动感觉,通常在海上旅行后出现。我们假设存在一种作为振荡器的神经元机制,即一种适应性内部模型,它或许能够抵消因波动而在船上经历的姿势正弦干扰。此后,我们将此机制确定为一个跨前庭核与小脑绒球小结叶的多回路神经网络。我们证明,这个回路系统有振荡倾向,且随着神经元连接强度的增加而增强。因此,我们推测突触可塑性,特别是长时程增强,可能在使这些振荡的阻尼变差中起作用。最后,我们假设在围绝经期女性中受到调节的神经调质降钙素基因相关肽会加剧这一过程,从而使这种转变不可逆,进而导致MdDS。鉴于MdDS患者与涉及起伏被动运动的海上旅行之间存在高度相关性,以及患者再次暴露于类似被动运动时症状会减轻,这种变得有害地持久的振荡器概念可作为MdDS的一个模型。可以利用姿势描记测试进一步研究该机制,以评估运动的主观感知是否与客观姿势不稳定相匹配。可以通过激素谱筛查来研究使个体更易患MdDS的神经化学失衡。可以通过神经成像技术以及经颅磁刺激来探索前庭核与小脑之间连接的改变,特别是γ-氨基丁酸能纤维。如果我们的假说得到检验和验证,那么在被认为在回路功能和突触可塑性中起基本作用的神经网络和生化因素中,就可以找到MdDS治疗的最佳靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/1769596d050d/fneur-11-576860-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/f8600b3fccb8/fneur-11-576860-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/7c4b03bad271/fneur-11-576860-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/1769596d050d/fneur-11-576860-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/f8600b3fccb8/fneur-11-576860-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/7c4b03bad271/fneur-11-576860-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f664/7683778/1769596d050d/fneur-11-576860-g0003.jpg

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Med Hypotheses. 2018 Nov;120:128-134. doi: 10.1016/j.mehy.2018.08.024. Epub 2018 Aug 29.