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膜去极化介导了高频刺激引起的神经活动抑制和细胞类型差异反应。

Membrane depolarization mediates both the inhibition of neural activity and cell-type-differences in response to high-frequency stimulation.

机构信息

Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Institute of Biomedical Electronics, TU Wien, Vienna, Austria.

出版信息

Commun Biol. 2024 Jun 18;7(1):734. doi: 10.1038/s42003-024-06359-3.

DOI:10.1038/s42003-024-06359-3
PMID:38890481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11189419/
Abstract

Neuromodulation using high frequency (>1 kHz) electric stimulation (HFS) enables preferential activation or inhibition of individual neural types, offering the possibility of more effective treatments across a broad spectrum of neurological diseases. To improve effectiveness, it is important to better understand the mechanisms governing activation and inhibition with HFS so that selectivity can be optimized. In this study, we measure the membrane potential (V) and spiking responses of ON and OFF α-sustained retinal ganglion cells (RGCs) to a wide range of stimulus frequencies (100-2500 Hz) and amplitudes (10-100 µA). Our findings indicate that HFS induces shifts in V, with both the strength and polarity of the shifts dependent on the stimulus conditions. Spiking responses in each cell directly correlate with the shifts in V, where strong depolarization leads to spiking suppression. Comparisons between the two cell types reveal that ON cells are more depolarized by a given amplitude of HFS than OFF cells-this sensitivity difference enables the selective targeting. Computational modeling indicates that ion-channel dynamics largely account for the shifts in V, suggesting that a better understanding of the differences in ion-channel properties across cell types may improve the selectivity and ultimately, enhance HFS-based neurostimulation strategies.

摘要

利用高频(>1 kHz)电刺激(HFS)进行神经调节可以优先激活或抑制单个神经类型,从而为广泛的神经疾病提供更有效的治疗方法。为了提高疗效,重要的是要更好地理解 HFS 控制激活和抑制的机制,以便优化选择性。在这项研究中,我们测量了广泛刺激频率(100-2500 Hz)和幅度(10-100 μA)下的 ON 和 OFF α 维持性视网膜神经节细胞(RGC)的膜电位(V)和尖峰反应。我们的发现表明,HFS 会引起 V 的偏移,偏移的强度和极性都取决于刺激条件。每个细胞的尖峰反应与 V 的偏移直接相关,其中强烈的去极化会导致尖峰抑制。两种细胞类型的比较表明,ON 细胞比 OFF 细胞更容易被给定幅度的 HFS 去极化——这种敏感性差异使选择性靶向成为可能。计算模型表明,离子通道动力学在很大程度上解释了 V 的偏移,这表明对跨细胞类型的离子通道特性差异有更好的理解可能会提高选择性,并最终增强基于 HFS 的神经刺激策略。

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Non-monotonic kilohertz frequency neural block thresholds arise from amplitude- and frequency-dependent charge imbalance.非单调千赫兹频率神经阻滞阈值源于幅度和频率相关的电荷失衡。
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