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从头痛到意外猝死:对扩散性抑制的理解

Understanding Spreading Depression from Headache to Sudden Unexpected Death.

作者信息

Cozzolino Olga, Marchese Maria, Trovato Francesco, Pracucci Enrico, Ratto Gian Michele, Buzzi Maria Gabriella, Sicca Federico, Santorelli Filippo M

机构信息

NEST, Istituto Nanoscienze CNR and Scuola Normale Superiore, Pisa, Italy.

Molecular Medicine and Clinical Neurophysiology Laboratories, Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.

出版信息

Front Neurol. 2018 Feb 1;9:19. doi: 10.3389/fneur.2018.00019. eCollection 2018.

Abstract

Spreading depression (SD) is a neurophysiological phenomenon characterized by abrupt changes in intracellular ion gradients and sustained depolarization of neurons. It leads to loss of electrical activity, changes in the synaptic architecture, and an altered vascular response. Although SD is often described as a unique phenomenon with homogeneous characteristics, it may be strongly affected by the particular triggering event and by genetic background. Furthermore, SD may contribute differently to the pathogenesis of widely heterogeneous clinical conditions. Indeed, clinical disorders related to SD vary in their presentation and severity, ranging from benign headache conditions (migraine syndromes) to severely disabling events, such as cerebral ischemia, or even death in people with epilepsy. Although the characteristics and mechanisms of SD have been dissected using a variety of approaches, ranging from cells to human models, this phenomenon remains only partially understood because of its complexity and the difficulty of obtaining direct experimental data. Currently, clinical monitoring of SD is limited to patients who require neurosurgical interventions and the placement of subdural electrode strips. Significantly, SD events recorded in humans display electrophysiological features that are essentially the same as those observed in animal models. Further research using existing and new experimental models of SD may allow a better understanding of its core mechanisms, and of their differences in different clinical conditions, fostering opportunities to identify and develop targeted therapies for SD-related disorders and their worst consequences.

摘要

扩散性抑制(SD)是一种神经生理现象,其特征为细胞内离子梯度的突然变化以及神经元的持续去极化。它会导致电活动丧失、突触结构改变以及血管反应改变。尽管SD通常被描述为一种具有同质特征的独特现象,但它可能会受到特定触发事件和遗传背景的强烈影响。此外,SD可能对广泛异质性临床病症的发病机制有不同的贡献。事实上,与SD相关的临床病症在表现和严重程度上各不相同,从良性头痛病症(偏头痛综合征)到严重致残事件,如脑缺血,甚至在癫痫患者中导致死亡。尽管已经使用从细胞到人体模型等多种方法剖析了SD的特征和机制,但由于其复杂性以及获取直接实验数据的困难,这种现象仍仅被部分理解。目前,SD的临床监测仅限于需要神经外科干预和放置硬膜下电极条的患者。值得注意的是,在人类中记录到的SD事件显示出与在动物模型中观察到的基本相同的电生理特征。使用现有的和新的SD实验模型进行进一步研究,可能有助于更好地理解其核心机制,以及它们在不同临床病症中的差异,从而为识别和开发针对与SD相关病症及其最严重后果的靶向治疗创造机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34aa/5799941/03e1a8f79199/fneur-09-00019-g001.jpg

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