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电生理学中频谱响应的神经团模型。

A neural mass model of spectral responses in electrophysiology.

作者信息

Moran R J, Kiebel S J, Stephan K E, Reilly R B, Daunizeau J, Friston K J

机构信息

The Wellcome Trust Centre for Neuroimaging, Institute of Neurology, University College London, 12 Queen Square, London, WC1N 3BG, UK.

出版信息

Neuroimage. 2007 Sep 1;37(3):706-20. doi: 10.1016/j.neuroimage.2007.05.032. Epub 2007 May 31.

DOI:10.1016/j.neuroimage.2007.05.032
PMID:17632015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2644418/
Abstract

We present a neural mass model of steady-state membrane potentials measured with local field potentials or electroencephalography in the frequency domain. This model is an extended version of previous dynamic causal models for investigating event-related potentials in the time-domain. In this paper, we augment the previous formulation with parameters that mediate spike-rate adaptation and recurrent intrinsic inhibitory connections. We then use linear systems analysis to show how the model's spectral response changes with its neurophysiological parameters. We demonstrate that much of the interesting behaviour depends on the non-linearity which couples mean membrane potential to mean spiking rate. This non-linearity is analogous, at the population level, to the firing rate-input curves often used to characterize single-cell responses. This function depends on the model's gain and adaptation currents which, neurobiologically, are influenced by the activity of modulatory neurotransmitters. The key contribution of this paper is to show how neuromodulatory effects can be modelled by adding adaptation currents to a simple phenomenological model of EEG. Critically, we show that these effects are expressed in a systematic way in the spectral density of EEG recordings. Inversion of the model, given such non-invasive recordings, should allow one to quantify pharmacologically induced changes in adaptation currents. In short, this work establishes a forward or generative model of electrophysiological recordings for psychopharmacological studies.

摘要

我们提出了一种在频域中用局部场电位或脑电图测量的稳态膜电位神经团模型。该模型是先前用于研究时域中事件相关电位的动态因果模型的扩展版本。在本文中,我们用介导脉冲率适应和递归内在抑制连接的参数扩充了先前的公式。然后,我们使用线性系统分析来展示模型的频谱响应如何随其神经生理参数变化。我们证明,许多有趣的行为取决于将平均膜电位与平均脉冲率耦合的非线性。在群体水平上,这种非线性类似于常用于表征单细胞反应的发放率-输入曲线。该函数取决于模型的增益和适应电流,从神经生物学角度来看,这些电流受调制性神经递质活动的影响。本文的关键贡献在于展示了如何通过向一个简单的脑电图现象学模型添加适应电流来模拟神经调节效应。至关重要的是,我们表明这些效应在脑电图记录的频谱密度中以一种系统的方式表现出来。在有此类非侵入性记录的情况下,对模型进行反演应该能够量化药物诱导的适应电流变化。简而言之,这项工作为精神药理学研究建立了一个电生理记录的正向或生成模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/ab01252038e2/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/bd09bd69ec62/gr1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/33a2d95f0e8f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/fff88ea60063/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/6e7316de4b7e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/8aa95555ae40/gr7ac.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/ab01252038e2/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/bd09bd69ec62/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/9f024ea63fa1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/35be7969f5c4/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/33a2d95f0e8f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/fff88ea60063/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/6e7316de4b7e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/8aa95555ae40/gr7ac.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/2829270/ab01252038e2/gr8.jpg

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