在轴突实验和模拟研究中,高频刺激期间阴极和阳极脉冲之间的相互作用以及极性交替的单相脉冲。

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL Journal of neural engineering Pub Date : 2023-09-26 DOI:10.1088/1741-2552/acf959
Yifan Hu, Zhouyan Feng, Lvpiao Zheng, Xiangyu Ye
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引用次数: 0

摘要

背景神经调控电疗法通常利用双相脉冲的高频刺激(HFS)来治疗神经疾病。双相脉冲由激活神经元的领先阴极相和平衡电荷的滞后阳极相组成。由于单相阴极脉冲和阳极脉冲都可以使神经元膜去极化,因此将双相脉冲分为交替的阴极脉冲和阴极脉冲可能是提高刺激效率的可行策略。客观的我们推测,在交替单相脉冲的持续HFS期间,最初由两个极性脉冲激活的体积中的神经元可能会改变为仅由阳极脉冲激活。为了验证这一假设,我们研究了HFS过程中单相脉冲的相互作用,并揭示了可能的潜在机制。方法在体内麻醉大鼠的海马CA1区,对肺泡纤维(即CA1锥体神经元的轴突)施加不同类型的脉冲刺激以抗损伤地激活神经元细胞体。使用交替的单相脉冲或双相脉冲施加抗变色HFS(A-HFS)序列。A-HFS序列中的脉冲频率为50或100Hz。A-HFS持续时间为120s。测量抗损伤诱发的群体尖峰的振幅,以评估每个脉冲诱导的神经元放电。使用轴突的计算模型来探索神经元调节的可能机制。分析了持续A-HFS过程中模型变量的变化。主要结果。在大鼠实验中,在相同脉冲强度下,阴极脉冲的激活体积大于阳极脉冲的激活容量。在成对脉冲测试中,前一个阴极脉冲能够防止后一个阳极脉冲由于不应期而激活神经元。这表明阴极脉冲的激活体积覆盖了阳极脉冲的激活容量。然而,在交替单相脉冲的持续A-HFS期间,在重叠的激活体积中,阳极脉冲能够优先于阴极脉冲来激活神经元。模型模拟结果揭示了阴极脉冲激活失效的机理。它们包括钾离子积累引起的过度膜去极化、传导途径中的超极化障碍以及阳极脉冲的相互作用。意义该研究首次表明,在持续HFS过程中,阳极脉冲在激活神经元的竞争中占主导地位。这一发现为设计HFS范式以提高神经调控疗法的效率提供了新的线索。
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Interactions between cathodic- and anodic-pulses during high-frequency stimulations with the monophasic-pulses alternating in polarity at axons-experiment and simulation studies.

Background. Electrical neuromodulation therapies commonly utilize high-frequency stimulations (HFS) of biphasic-pulses to treat neurological disorders. The biphasic pulse consists of a leading cathodic-phase to activate neurons and a lagging anodic-phase to balance electrical charges. Because both monophasic cathodic- and anodic-pulses can depolarize neuronal membranes, splitting biphasic-pulses into alternate cathodic- and anodic-pulses could be a feasible strategy to improve stimulation efficiency.Objective. We speculated that neurons in the volume initially activated by both polarity pulses could change to be activated only by anodic-pulses during sustained HFS of alternate monophasic-pulses. To verify the hypothesis, we investigated the interactions of the monophasic pulses during HFS and revealed possible underlying mechanisms.Approach. Different types of pulse stimulations were applied at the alvear fibers (i.e. the axons of CA1 pyramidal neurons) to antidromically activate the neuronal cell bodies in the hippocampal CA1 region of anesthetized ratsin-vivo. Sequences of antidromic HFS (A-HFS) were applied with alternate monophasic-pulses or biphasic-pulses. The pulse frequency in the A-HFS sequences was 50 or 100 Hz. The A-HFS duration was 120 s. The amplitude of antidromically-evoked population spike was measured to evaluate the neuronal firing induced by each pulse. A computational model of axon was used to explore the possible mechanisms of neuronal modulations. The changes of model variables during sustained A-HFS were analyzed.Main results. In rat experiments, with a same pulse intensity, the activation volume of a cathodic-pulse was greater than that of an anodic-pulse. In paired-pulse tests, a preceding cathodic-pulse was able to prevent a following anodic-pulse from activating neurons due to refractory period. This indicated that the activation volume of a cathodic-pulse covered that of an anodic-pulse. However, during sustained A-HFS of alternate monophasic-pulses, the anodic-pulses were able to prevail over the cathodic-pulses in activating neurons in the overlapped activation volume. Model simulation results show the mechanisms of the activation failures of cathodic-pulses. They include the excessive membrane depolarization caused by an accumulation of potassium ions, the obstacle of hyperpolarization in the conduction pathway and the interactions from anodic-pulses.Significance. The study firstly showed the domination of anodic-pulses over cathodic-pulses in their competitions to activate neurons during sustained HFS. The finding provides new clues for designing HFS paradigms to improve the efficiency of neuromodulation therapies.

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来源期刊
Journal of neural engineering
Journal of neural engineering 工程技术-工程:生物医学
CiteScore
7.80
自引率
12.50%
发文量
319
审稿时长
4.2 months
期刊介绍: The goal of Journal of Neural Engineering (JNE) is to act as a forum for the interdisciplinary field of neural engineering where neuroscientists, neurobiologists and engineers can publish their work in one periodical that bridges the gap between neuroscience and engineering. The journal publishes articles in the field of neural engineering at the molecular, cellular and systems levels. The scope of the journal encompasses experimental, computational, theoretical, clinical and applied aspects of: Innovative neurotechnology; Brain-machine (computer) interface; Neural interfacing; Bioelectronic medicines; Neuromodulation; Neural prostheses; Neural control; Neuro-rehabilitation; Neurorobotics; Optical neural engineering; Neural circuits: artificial & biological; Neuromorphic engineering; Neural tissue regeneration; Neural signal processing; Theoretical and computational neuroscience; Systems neuroscience; Translational neuroscience; Neuroimaging.
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