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癫痫性猝死模型中过度兴奋的上丘与致命性脑干扩散性去极化

Hyperexcitable superior colliculus and fatal brainstem spreading depolarization in a model of Sudden Unexpected Death in Epilepsy.

作者信息

Cain Stuart M, Bernier Louis-Philippe, Zhang Yiming, Yung Andrew C, Kass Jennifer, Bohnet Barry, Yang Yi, Gopaul Rayshad, Kozlowski Piotr, MacVicar Brian A, Snutch Terrance P

机构信息

Djavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, Canada.

Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.

出版信息

Brain Commun. 2022 Jan 19;4(2):fcac006. doi: 10.1093/braincomms/fcac006. eCollection 2022.

Abstract

Cardiorespiratory arrest and death in mouse models of sudden unexpected death in epilepsy occur when spreading depolarization is triggered by cortical seizures and then propagates to the brainstem. However, the critical brain regions and the specific changes required to allow spreading depolarization to propagate to the brainstem under the relatively rare circumstances leading to a fatal seizure are unknown. We previously found that following cortical seizure-inducing electrical stimulation, spreading depolarization could occur in both the superior and inferior colliculi in Cacna1a mice, but was never observed in wild-type animals or following non-seizure-inducing stimuli in Cacna1a mice. Here, we show that optogenetic stimulation of the superior/inferior colliculi in Cacna1a mice induces severe seizures, and resulting spreading depolarization in the superior/inferior colliculi that propagates to the brainstem and correlates with the respiratory arrest followed by cardiac arrest. Further, we show that neurons of the superior colliculus in Cacna1a mice exhibit hyperexcitable properties that we propose underlie a distinct susceptibility to spreading depolarization. Our data suggest that the susceptibility of the superior colliculus to elicit fatal spreading depolarization is a result of either genetic or seizure-related alterations within the superior colliculus that may involve changes to structure, connectivity and/or excitability.

摘要

在癫痫性猝死的小鼠模型中,当皮层癫痫发作引发扩散性去极化并传播至脑干时,会发生心肺骤停和死亡。然而,在导致致命性癫痫发作的相对罕见情况下,允许扩散性去极化传播至脑干所需的关键脑区和特定变化尚不清楚。我们之前发现,在皮层癫痫诱发电刺激后,Cacna1a小鼠的上丘和下丘均可发生扩散性去极化,但在野生型动物或Cacna1a小鼠的非癫痫诱发刺激后从未观察到这种情况。在此,我们表明,对Cacna1a小鼠的上丘/下丘进行光遗传学刺激会诱发严重癫痫发作,并导致上丘/下丘中产生的扩散性去极化传播至脑干,且与随后的呼吸骤停和心脏骤停相关。此外,我们表明,Cacna1a小鼠上丘的神经元表现出过度兴奋的特性,我们认为这是对扩散性去极化具有独特易感性的基础。我们的数据表明,上丘引发致命性扩散性去极化的易感性是上丘内遗传或癫痫相关改变的结果,这些改变可能涉及结构、连接性和/或兴奋性的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2795/9035526/bc1f940481ef/fcac006ga1.jpg

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