Response of neuronal populations to phase-locked stimulation: model-based predictions and validation.

IF 4 2区 医学 Q1 NEUROSCIENCES Journal of Neuroscience Pub Date : 2025-03-11 DOI:10.1523/JNEUROSCI.2269-24.2025
Nima Mirkhani, Colin G McNamara, Gaspard Oliviers, Andrew Sharott, Benoit Duchet, Rafal Bogacz
{"title":"Response of neuronal populations to phase-locked stimulation: model-based predictions and validation.","authors":"Nima Mirkhani, Colin G McNamara, Gaspard Oliviers, Andrew Sharott, Benoit Duchet, Rafal Bogacz","doi":"10.1523/JNEUROSCI.2269-24.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Modulation of neuronal oscillations holds promise for the treatment of neurological disorders. Nonetheless, conventional stimulation in a continuous open-loop manner can lead to side effects and suboptimal efficiency. Closed-loop strategies such as phase-locked stimulation aim to address these shortcomings by offering a more targeted modulation. While theories have been developed to understand the neural response to stimulation, their predictions have not been thoroughly tested using experimental data. Using a mechanistic coupled oscillator model, we elaborate on two key predictions describing the response to stimulation as a function of the phase and amplitude of ongoing neural activity. To investigate these predictions, we analyze electrocorticogram recordings from a previously conducted study in Parkinsonian rats, and extract the corresponding phase and response curves. We demonstrate that the amplitude response to stimulation is strongly correlated to the derivative of the phase response ([Formula: see text] > 0.8) in all animals except one, thereby validating a key model prediction. The second prediction postulates that the stimulation becomes ineffective when the network synchrony is high, a trend that appeared missing in the data. Our analysis explains this discrepancy by showing that the neural populations in Parkinsonian rats did not reach the level of synchrony for which the theory would predict ineffective stimulation. Our results highlight the potential of fine-tuning stimulation paradigms informed by mathematical models that consider both the ongoing phase and amplitude of the targeted neural oscillation.<b>Significance Statement</b> This study validates a mathematical model of coupled oscillators in predicting the response of neural activity to stimulation for the first time. Our findings also offer further insights beyond this validation. For instance, the demonstrated correlation between phase response and amplitude response is indeed a key theoretical concept within a subset of mathematical models. This prediction can bring about clinical implications in terms of predictive power for manipulation of neural activity. Additionally, while phase dependence in modulation has been previously studied, we propose a general framework for studying amplitude dependence as well. Lastly, our study reconciles the seemingly contradictory views of pathologic hypersynchrony and theoretical low synchrony in Parkinson's disease.</p>","PeriodicalId":50114,"journal":{"name":"Journal of Neuroscience","volume":" ","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11984083/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1523/JNEUROSCI.2269-24.2025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Modulation of neuronal oscillations holds promise for the treatment of neurological disorders. Nonetheless, conventional stimulation in a continuous open-loop manner can lead to side effects and suboptimal efficiency. Closed-loop strategies such as phase-locked stimulation aim to address these shortcomings by offering a more targeted modulation. While theories have been developed to understand the neural response to stimulation, their predictions have not been thoroughly tested using experimental data. Using a mechanistic coupled oscillator model, we elaborate on two key predictions describing the response to stimulation as a function of the phase and amplitude of ongoing neural activity. To investigate these predictions, we analyze electrocorticogram recordings from a previously conducted study in Parkinsonian rats, and extract the corresponding phase and response curves. We demonstrate that the amplitude response to stimulation is strongly correlated to the derivative of the phase response ([Formula: see text] > 0.8) in all animals except one, thereby validating a key model prediction. The second prediction postulates that the stimulation becomes ineffective when the network synchrony is high, a trend that appeared missing in the data. Our analysis explains this discrepancy by showing that the neural populations in Parkinsonian rats did not reach the level of synchrony for which the theory would predict ineffective stimulation. Our results highlight the potential of fine-tuning stimulation paradigms informed by mathematical models that consider both the ongoing phase and amplitude of the targeted neural oscillation.Significance Statement This study validates a mathematical model of coupled oscillators in predicting the response of neural activity to stimulation for the first time. Our findings also offer further insights beyond this validation. For instance, the demonstrated correlation between phase response and amplitude response is indeed a key theoretical concept within a subset of mathematical models. This prediction can bring about clinical implications in terms of predictive power for manipulation of neural activity. Additionally, while phase dependence in modulation has been previously studied, we propose a general framework for studying amplitude dependence as well. Lastly, our study reconciles the seemingly contradictory views of pathologic hypersynchrony and theoretical low synchrony in Parkinson's disease.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
神经元群体对锁相刺激的反应:基于模型的预测和验证。
神经振荡的调节为神经系统疾病的治疗带来了希望。然而,传统的连续开环增产方式可能会导致副作用和效率不佳。锁相激励等闭环策略旨在通过提供更有针对性的调制来解决这些缺点。虽然已经发展了一些理论来理解神经对刺激的反应,但他们的预测还没有经过实验数据的彻底检验。利用机械耦合振荡器模型,我们详细阐述了两个关键预测,描述了对刺激的反应是正在进行的神经活动的相位和振幅的函数。为了研究这些预测,我们分析了先前在帕金森大鼠中进行的一项研究的皮质电图记录,并提取了相应的相位和反应曲线。我们证明,除了一只动物外,所有动物对刺激的振幅响应都与相位响应的导数([公式:见文本]>.8)密切相关,从而验证了一个关键的模型预测。第二个预测假设,当网络同步性高时,刺激变得无效,这一趋势在数据中似乎缺失。我们的分析通过显示帕金森大鼠的神经群没有达到理论预测无效刺激的同步水平来解释这种差异。我们的研究结果强调了微调刺激范式的潜力,该模型考虑了目标神经振荡的持续相位和振幅。本研究首次验证了耦合振荡器的数学模型在预测神经活动对刺激的反应方面的作用。我们的研究结果还提供了进一步的见解,超出了这一验证。例如,相位响应和幅度响应之间的相关性确实是数学模型子集中的一个关键理论概念。这一预测在神经活动操控的预测能力方面具有临床意义。此外,虽然先前已经研究了调制中的相位依赖性,但我们也提出了研究幅度依赖性的一般框架。最后,我们的研究调和了帕金森氏病的病理性高同步性和理论低同步性的看似矛盾的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
期刊最新文献
Increased and coupled ERP and fMRI responses towards positive social evaluative feedback: An EEG-fMRI study. Anesthetic State-Dependent Bidirectional Control of States of Consciousness via Heterogeneous Medial Septum to Ventral Tegmental Area Circuits under Sevoflurane in Mice. Temporally coordinated activity among motor cortex, thalamus, and thalamic reticular nucleus neurons during rat forelimb movements. Corticotropin-releasing factor and somatostatin neurons in the central amygdala mediate dynamic defensive behaviors during fear extinction. The Parafascicular Role in Updating Action from a Spatial to a Visual Strategy is Driven by its Glutamatergic Mesencephalic Locomotor Region inputs.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1