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快速和慢速皮质振荡对弥漫性去极化抑制作用的不同易损性:与偏头痛先兆发病机制相关的状态依赖性特征。

Different vulnerability of fast and slow cortical oscillations to suppressive effect of spreading depolarization: state-dependent features potentially relevant to pathogenesis of migraine aura.

机构信息

Department of Molecular Neurobiology, Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, Butlerova Street 5A, 117485, Moscow, Russia.

Department of Conditioned Reflexes and Physiology of Emotion, Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, Butlerova Street 5A, 117485, Moscow, Russia.

出版信息

J Headache Pain. 2024 Jan 15;25(1):8. doi: 10.1186/s10194-023-01706-x.

Abstract

BACKGROUND

Spreading depolarization (SD), underlying mechanism of migraine aura and potential activator of pain pathways, is known to elicit transient local silencing cortical activity. Sweeping across the cortex, the electrocorticographic depression is supposed to underlie spreading negative symptoms of migraine aura. Main information about the suppressive effect of SD on cortical oscillations was obtained in anesthetized animals while ictal recordings in conscious patients failed to detect EEG depression during migraine aura. Here, we investigate the suppressive effect of SD on spontaneous cortical activity in awake animals and examine whether the anesthesia modifies the SD effect.

METHODS

Spectral and spatiotemporal characteristics of spontaneous cortical activity following a single unilateral SD elicited by amygdala pinprick were analyzed in awake freely behaving rats and after induction of urethane anesthesia.

RESULTS

In wakefulness, SD transiently suppressed cortical oscillations in all frequency bands except delta. Slow delta activity did not decline its power during SD and even increased it afterwards; high-frequency gamma oscillations showed the strongest and longest depression under awake conditions. Unexpectedly, gamma power reduced not only during SD invasion the recording cortical sites but also when SD occupied distant subcortical/cortical areas. Contralateral cortex not invaded by SD also showed transient depression of gamma activity in awake animals. Introduction of general anesthesia modified the pattern of SD-induced depression: SD evoked the strongest cessation of slow delta activity, milder suppression of fast oscillations and no distant changes in gamma activity.

CONCLUSION

Slow and fast cortical oscillations differ in their vulnerability to SD influence, especially in wakefulness. In the conscious brain, SD produces stronger and spatially broader depression of fast cortical oscillations than slow ones. The frequency-specific effects of SD on cortical activity of awake brain may underlie some previously unexplained clinical features of migraine aura.

摘要

背景

扩散性去极化(SD)是偏头痛先兆的潜在疼痛通路激活因子,已知其会引起皮质活动的短暂性局部抑制。这种电皮质抑制在大脑皮层上扫过,据推测是偏头痛先兆扩散性负症状的基础。关于 SD 对皮质振荡的抑制作用的主要信息是在麻醉动物中获得的,而在清醒患者的癫痫发作记录中未能在偏头痛先兆期间检测到 EEG 抑制。在这里,我们研究了 SD 对清醒动物自发皮质活动的抑制作用,并检查了麻醉是否会改变 SD 效应。

方法

通过对清醒自由活动的大鼠进行单侧杏仁核针刺诱发单次单侧 SD,分析 SD 后自发皮质活动的频谱和时空特征,并在诱导使用氨基甲酸乙酯麻醉后进行分析。

结果

在清醒状态下,SD 短暂地抑制了所有频段的皮质振荡,除了 delta 频段。慢 delta 活动在 SD 期间并没有降低其功率,甚至在之后还增加了;高频 gamma 振荡在清醒状态下表现出最强和最长的抑制。出乎意料的是,gamma 功率不仅在 SD 入侵记录皮质部位期间降低,而且在 SD 占据远处的皮质/皮质下区域时也降低。未被 SD 入侵的对侧皮质在清醒动物中也表现出 gamma 活动的短暂抑制。全身麻醉的引入改变了 SD 诱导的抑制模式:SD 引起的慢 delta 活动最强的停止,快速振荡的抑制更温和,gamma 活动没有远处的变化。

结论

慢和快皮质振荡在对 SD 影响的敏感性方面存在差异,尤其是在清醒状态下。在清醒大脑中,SD 引起的快速皮质振荡的抑制比慢振荡更强且空间更广泛。SD 对清醒大脑皮质活动的频率特异性影响可能是偏头痛先兆一些先前未解释的临床特征的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c729/10789028/0c8ea071210f/10194_2023_1706_Fig1_HTML.jpg

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