Understanding Spreading Depression from Headache to Sudden Unexpected Death

被引:51
作者
Cozzolino, Olga [1 ,2 ]
Marchese, Maria [3 ]
Trovato, Francesco [1 ,2 ]
Pracucci, Enrico [1 ,2 ]
Ratto, Gian Michele [1 ,2 ]
Buzzi, Maria Gabriella [4 ,5 ]
Sicca, Federico [3 ]
Santorelli, Filippo M. [3 ]
机构
[1] CNR, NEST, Ist Nanosci, Pisa, Italy
[2] Scuola Normale Super Pisa, Pisa, Italy
[3] IRCCS Fdn Stella Maris, Dept Dev Neurosci, Mol Med & Clin Neurophysiol Labs, Pisa, Italy
[4] Fdn Santa Lucia, Headache Ctr, Rome, Italy
[5] Fdn Santa Lucia, Postcoma Unit IRCCS, Rome, Italy
来源
FRONTIERS IN NEUROLOGY | 2018年 / 9卷
关键词
spreading depression; spreading depolarization; migraine; ischemia; subarachnoid hemorrhage; epilepsy; sudden unexpected death in epilepsy; FAMILIAL HEMIPLEGIC MIGRAINE; ISCHEMIC NEUROLOGICAL DEFICITS; TRAUMATIC BRAIN-INJURY; IN-VIVO; EXTRACELLULAR-SPACE; CEREBRAL-ISCHEMIA; MOUSE MODEL; BLOOD-FLOW; SUBARACHNOID HEMORRHAGE; CHLORIDE COTRANSPORTERS;
D O I
10.3389/fneur.2018.00019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
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页数:13
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