表征人类海马皮层网络中神经元和群体对电刺激的反应。

IF 8.4 1区 医学 Q1 CLINICAL NEUROLOGY
Mircea van der Plas , Frederic Roux , Ramesh Chelvarajah , Vijay Sawlani , Bernhard Staresina , Maria Wimber , David T. Rollings , Simon Hanslmayr
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引用次数: 0

摘要

背景:海马是直接电刺激(DES)的常见靶点。虽然大量的研究集中在各种刺激方案的临床结果上,但DES在人类海马体中的精确神经动力学仍然知之甚少,限制了我们建模和预测海马体神经活动的能力。传统的立体定向电极提供的信息有限,因为在DES过程中记录的信号变得饱和,只能记录足够远区域的LFP活动。Behnke-Fried电极绕过了这一限制,能够在刺激期间同时记录局部海马单单元和LFP活动。目的:我们的目的是在单神经元和群体水平上表征海马和周围皮层区域对单脉冲DES的神经反应。方法:我们收集了7例癫痫患者的34个海马植入的Behnke-Fried电极的数据。这种独特的方法使我们能够监测海马和周围新皮质响应1ms双极单脉冲DES的局部场电位和单个神经元活动(N=136)。单脉冲系统地通过电极导线在新皮层终止,使我们能够评估局部反应和网络传播效应。结果:尽管刺激强度很高,但只有29%的单个单元对海马刺激表现出可测量的反应。反应性神经元表现出一种刻板模式:最初的兴奋性反应(簇大小:110 ms, p = 0.0017),然后是减少放电的抑制性“沉默期”(簇大小:141 ms, p < 0.0005)。初始兴奋强度和沉默时间均与距离刺激点的距离呈负相关(峰值高度r = -0.94, p < 0.0001;沉默时间r = -0.93, p < 0.0001)。LFP反应在时域和频域都证实了这些发现。值得注意的是,海马对新皮层刺激的反应显示出大约100毫秒的持续滞后。最后,我们发现皮层对海马刺激的反应受到刺激时海马theta相的调节。结论:我们首次在人类海马-皮层网络的神经元和群体水平上全面描述了海马对DES的反应。我们对刻板反应模式和可量化的相位依赖网络效应的研究结果为未来针对人类记忆系统的刺激范式提供了重要参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterizing neuronal and population responses to electrical stimulation in the human hippocampo-cortical network

Background

The hippocampus is a common target for direct electrical stimulation (DES). While considerable research has focused on clinical outcomes of various stimulation protocols, the precise neural dynamics of DES in the human hippocampus remain poorly understood, limiting our ability to model and predict hippocampal neural activity. Conventional stereotactic electrodes provide limited insight as the recorded signal becomes saturated during DES, allowing to only record LFP activity from stimulation in sufficiently distant areas. Behnke-Fried electrodes circumvent this limitation, enabling simultaneous recording of local hippocampal single-unit and LFP activity during stimulation.

Objective

We aimed to characterize the neural responses to single pulse DES in the hippocampus and surrounding cortical areas at both single-neuron and population levels.

Methods

We collected data from 34 hippocampally implanted Behnke-Fried electrodes across seven epilepsy patients. This unique approach allowed us to monitor both local field potentials and single neuron activity (N = 136) in response to 1 ms bipolar single pulse DES in the hippocampus and surrounding neocortex. Single pulses were administered systematically across electrode leads terminating in the neocortex, allowing us to assess both local responses and network propagation effects.

Results

Despite high stimulation intensity, only 29 % of single units exhibited measurable responses to hippocampal stimulation. Responsive neurons displayed a stereotypical pattern: an initial excitatory response (cluster size: 110 ms, p = 0.0017) followed by an inhibitory 'silent period' of reduced firing (cluster size: 141 ms, p < 0.0005). Both the intensity of the initial excitation and the duration of the silent period were inversely correlated with distance from the stimulation site (peak height: r = −0.94, p < 0.0001; silent duration: r = −0.93, p < 0.0001). LFP responses corroborated these findings in both time and frequency domains. Notably, hippocampal responses to neocortical stimulation revealed a consistent lag of approximately 100 ms. Finally, we found evidence that cortical responses to hippocampal stimulation were modulated by hippocampal theta phase at the time of stimulation.

Conclusions

We provide the first comprehensive characterization of hippocampal responses to DES at both neuronal and population levels in the human hippocampo-cortical network. Our findings of stereotypical response patterns and quantifiable phase-dependent network effects provide crucial parameters to inform future stimulation paradigms targeting the human memory system.
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来源期刊
Brain Stimulation
Brain Stimulation 医学-临床神经学
CiteScore
13.10
自引率
9.10%
发文量
256
审稿时长
72 days
期刊介绍: Brain Stimulation publishes on the entire field of brain stimulation, including noninvasive and invasive techniques and technologies that alter brain function through the use of electrical, magnetic, radiowave, or focally targeted pharmacologic stimulation. Brain Stimulation aims to be the premier journal for publication of original research in the field of neuromodulation. The journal includes: a) Original articles; b) Short Communications; c) Invited and original reviews; d) Technology and methodological perspectives (reviews of new devices, description of new methods, etc.); and e) Letters to the Editor. Special issues of the journal will be considered based on scientific merit.
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