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受生理启发的多重Kuramoto模型描述了皮层活动的相图。

Physiologically motivated multiplex Kuramoto model describes phase diagram of cortical activity.

作者信息

Sadilek Maximilian, Thurner Stefan

机构信息

Section for Science of Complex Systems, Medical University of Vienna, Spitalgasse 23, A-1090 Vienna, Austria.

1] Section for Science of Complex Systems, Medical University of Vienna, Spitalgasse 23, A-1090 Vienna, Austria [2] Santa Fe Institute, 1399 Hyde Park Road, New Mexico 87501, USA [3] IIASA, Schlossplatz 1, A-2361 Laxenburg, Austria.

出版信息

Sci Rep. 2015 May 21;5:10015. doi: 10.1038/srep10015.

DOI:10.1038/srep10015
PMID:25996547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4650820/
Abstract

We derive a two-layer multiplex Kuramoto model from Wilson-Cowan type physiological equations that describe neural activity on a network of interconnected cortical regions. This is mathematically possible due to the existence of a unique, stable limit cycle, weak coupling, and inhibitory synaptic time delays. We study the phase diagram of this model numerically as a function of the inter-regional connection strength that is related to cerebral blood flow, and a phase shift parameter that is associated with synaptic GABA concentrations. We find three macroscopic phases of cortical activity: background activity (unsynchronized oscillations), epileptiform activity (highly synchronized oscillations) and resting-state activity (synchronized clusters/chaotic behaviour). Previous network models could hitherto not explain the existence of all three phases. We further observe a shift of the average oscillation frequency towards lower values together with the appearance of coherent slow oscillations at the transition from resting-state to epileptiform activity. This observation is fully in line with experimental data and could explain the influence of GABAergic drugs both on gamma oscillations and epileptic states. Compared to previous models for gamma oscillations and resting-state activity, the multiplex Kuramoto model not only provides a unifying framework, but also has a direct connection to measurable physiological parameters.

摘要

我们从描述相互连接的皮质区域网络上神经活动的威尔逊-考恩型生理方程中推导出一个两层多重库拉托莫模型。由于存在唯一的稳定极限环、弱耦合和抑制性突触时间延迟,这在数学上是可行的。我们将该模型的相图作为与脑血流量相关的区域间连接强度以及与突触γ-氨基丁酸(GABA)浓度相关的相移参数的函数进行数值研究。我们发现了皮质活动的三个宏观阶段:背景活动(非同步振荡)、癫痫样活动(高度同步振荡)和静息态活动(同步簇/混沌行为)。此前的网络模型迄今无法解释所有这三个阶段的存在。我们还进一步观察到,在从静息态活动向癫痫样活动转变时,平均振荡频率向更低值偏移,同时出现了相干的慢振荡。这一观察结果与实验数据完全一致,并且可以解释GABA能药物对γ振荡和癫痫状态的影响。与之前关于γ振荡和静息态活动的模型相比,多重库拉托莫模型不仅提供了一个统一的框架,而且与可测量的生理参数有直接联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/a0ddaa64c36b/srep10015-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/602f70b61651/srep10015-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/ca6e92315e91/srep10015-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/a0ddaa64c36b/srep10015-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/602f70b61651/srep10015-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/ca6e92315e91/srep10015-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2e/4650820/a0ddaa64c36b/srep10015-f3.jpg

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