scholarly journals The dynamics of resting fluctuations in the brain: metastability and its dynamical cortical core

2016 ◽  
Author(s):  
Gustavo Deco ◽  
Morten L. Kringelbach ◽  
Viktor K. Jirsa ◽  
Petra Ritter

AbstractIn the human brain, spontaneous activity during resting state consists of rapid transitions between functional network states over time but the underlying mechanisms are not understood. We use connectome based computational brain network modeling to reveal fundamental principles of how the human brain generates large-scale activity observable by noninvasive neuroimaging. By including individual structural and functional neuroimaging data into brain network models we construct personalized brain models. With this novel approach, we reveal that the human brain during resting state operates at maximum metastability, i.e. in a state of maximum network switching. In addition, we investigate cortical heterogeneity across areas. Optimization of the spectral characteristics of each local brain region revealed the dynamical cortical core of the human brain, which is driving the activity of the rest of the whole brain. Personalized brain network modelling goes beyond correlational neuroimaging analysis and reveals non-trivial network mechanisms underlying non-invasive observations. Our novel findings significantly pertain to the important role of computational connectomics in understanding principles of brain function.

2021 ◽  
Author(s):  
Mangor Pedersen ◽  
Andrew Zalesky

SummaryThe extent to which resting-state fMRI (rsfMRI) reflects direct neuronal changes remains unknown. Using 160 simultaneous rsfMRI and intracranial brain stimulation recordings acquired in 26 individuals with epilepsy (with varying electrode locations), we tested whether brain networks dynamically change during intracranial brain stimulation, aiming to establish whether switching between brain networks is reduced during intracranial brain stimulation. As the brain spontaneously switches between a repertoire of intrinsic functional network configurations and the rate of switching is typically increased in brain disorders, we hypothesised that intracranial stimulation would reduce the brain’s switching rate, thus potentially normalising aberrant brain network dynamics. To test this hypothesis, we quantified the rate that brain regions changed networks over time in response to brain stimulation, using network switching applied to multilayer modularity analysis of time-resolved rsfMRI connectivity. Network switching was significantly decreased during epochs with brain stimulation compared to epochs with no brain stimulation. The initial stimulation onset of brain stimulation was associated with the greatest decrease in network switching, followed by a more consistent reduction in network switching throughout the scans. These changes were most commonly observed in cortical networks spatially distant from the stimulation targets. Our results suggest that neuronal perturbation is likely to modulate large-scale brain networks, and multilayer network modelling may be used to inform the clinical efficacy of brain stimulation in neurological disease.HighlightsrsfMRI network switching is attenuated during intracranial brain stimulationStimulation-induced switching is observed distant from electrode targetsOur results are validated across a range of network parametersNetwork models may inform clinical efficacy of brain stimulation


Solid Earth ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 2159-2209
Author(s):  
Rahul Prabhakaran ◽  
Giovanni Bertotti ◽  
Janos Urai ◽  
David Smeulders

Abstract. Rock fractures organize as networks, exhibiting natural variation in their spatial arrangements. Therefore, identifying, quantifying, and comparing variations in spatial arrangements within network geometries are of interest when explicit fracture representations or discrete fracture network models are chosen to capture the influence of fractures on bulk rock behaviour. Treating fracture networks as spatial graphs, we introduce a novel approach to quantify spatial variation. The method combines graph similarity measures with hierarchical clustering and is applied to investigate the spatial variation within large-scale 2-D fracture networks digitized from the well-known Lilstock limestone pavements, Bristol Channel, UK. We consider three large, fractured regions, comprising nearly 300 000 fractures spread over 14 200 m2 from the Lilstock pavements. Using a moving-window sampling approach, we first subsample the large networks into subgraphs. Four graph similarity measures – fingerprint distance, D-measure, Network Laplacian spectral descriptor (NetLSD), and portrait divergence – that encapsulate topological relationships and geometry of fracture networks are then used to compute pair-wise subgraph distances serving as input for the statistical hierarchical clustering technique. In the form of hierarchical dendrograms and derived spatial variation maps, the results indicate spatial autocorrelation with localized spatial clusters that gradually vary over distances of tens of metres with visually discernable and quantifiable boundaries. Fractures within the identified clusters exhibit differences in fracture orientations and topology. The comparison of graph similarity-derived clusters with fracture persistence measures indicates an intra-network spatial variation that is not immediately obvious from the ubiquitous fracture intensity and density maps. The proposed method provides a quantitative way to identify spatial variations in fracture networks, guiding stochastic and geostatistical approaches to fracture network modelling.


2019 ◽  
Author(s):  
Steve Mehrkanoon

AbstractWhen the human brain manifests the birth of organised communication among local and large-scale neuronal populations activity remains undescribed. We report, in resting-state EEG source-estimates of 100 infants at term age, the existence of macro-scale dynamic functional connectivity, which have rich topological organisations, distinct spectral fingerprints and scale-invariance temporal dynamics. These functional networks encompass the default mode, primary sensory-limbic system, thalamo-frontal, thalamo-sensorimotor and visual-limbic system confined in the delta and low-alpha frequency intervals (1-8 Hz). The temporal dynamics of these networks not only are nested within much slower timescale (¡ 0.1 Hz) but also correlated in a hierarchical leading-following organisation. We show that the anatomically constrained richly organised spatial topologies, spectral contents and temporal fluctuations of resting-state networks reflect an established intrinsic dynamic functional connectome in the human brain at term age. The graph theoretical analysis of the spatial architectures of the networks revealed small-world topology and distinct rich-club organisations of interconnected cortical hubs that exhibit rich synchronous dynamics at multiple timescales. The approach opens new avenues to advance our understanding about the early configuration organisation of dynamic networks in the human brain and offers a novel monitoring platform to investigate functional brain network development in sick preterm infants.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Giuseppe Giacopelli ◽  
Domenico Tegolo ◽  
Emiliano Spera ◽  
Michele Migliore

AbstractThe brain’s structural connectivity plays a fundamental role in determining how neuron networks generate, process, and transfer information within and between brain regions. The underlying mechanisms are extremely difficult to study experimentally and, in many cases, large-scale model networks are of great help. However, the implementation of these models relies on experimental findings that are often sparse and limited. Their predicting power ultimately depends on how closely a model’s connectivity represents the real system. Here we argue that the data-driven probabilistic rules, widely used to build neuronal network models, may not be appropriate to represent the dynamics of the corresponding biological system. To solve this problem, we propose to use a new mathematical framework able to use sparse and limited experimental data to quantitatively reproduce the structural connectivity of biological brain networks at cellular level.


Author(s):  
Xerxes D. Arsiwalla ◽  
Riccardo Zucca ◽  
Alberto Betella ◽  
Enrique Martinez ◽  
David Dalmazzo ◽  
...  

2018 ◽  
Author(s):  
Amrit Kashyap ◽  
Shella Keilholz

AbstractBrain Network Models have become a promising theoretical framework in simulating signals that are representative of whole brain activity such as resting state fMRI. However, it has been difficult to compare the complex brain activity between simulated and empirical data. Previous studies have used simple metrics that surmise coordination between regions such as functional connectivity, and we extend on this by using various different dynamical analysis tools that are currently used to understand resting state fMRI. We show that certain properties correspond to the structural connectivity input that is shared between the models, and certain dynamic properties relate more to the mathematical description of the Brain Network Model. We conclude that the dynamic properties that gauge more temporal structure rather than spatial coordination in the rs-fMRI signal seem to provide the largest contrasts between different BNMs and the unknown empirical dynamical system. Our results will be useful in constraining and developing more realistic simulations of whole brain activity.


2018 ◽  
Author(s):  
RL van den Brink ◽  
S Nieuwenhuis ◽  
TH Donner

ABSTRACTThe widely projecting catecholaminergic (norepinephrine and dopamine) neurotransmitter systems profoundly shape the state of neuronal networks in the forebrain. Current models posit that the effects of catecholaminergic modulation on network dynamics are homogenous across the brain. However, the brain is equipped with a variety of catecholamine receptors with distinct functional effects and heterogeneous density across brain regions. Consequently, catecholaminergic effects on brain-wide network dynamics might be more spatially specific than assumed. We tested this idea through the analysis of functional magnetic resonance imaging (fMRI) measurements performed in humans (19 females, 5 males) at ‘rest’ under pharmacological (atomoxetine-induced) elevation of catecholamine levels. We used a linear decomposition technique to identify spatial patterns of correlated fMRI signal fluctuations that were either increased or decreased by atomoxetine. This yielded two distinct spatial patterns, each expressing reliable and specific drug effects. The spatial structure of both fluctuation patterns resembled the spatial distribution of the expression of catecholamine receptor genes: α1 norepinephrine receptors (for the fluctuation pattern: placebo > atomoxetine), ‘D2-like’ dopamine receptors (pattern: atomoxetine > placebo), and β norepinephrine receptors (for both patterns, with correlations of opposite sign). We conclude that catecholaminergic effects on the forebrain are spatially more structured than traditionally assumed and at least in part explained by the heterogeneous distribution of various catecholamine receptors. Our findings link catecholaminergic effects on large-scale brain networks to low-level characteristics of the underlying neurotransmitter systems. They also provide key constraints for the development of realistic models of neuromodulatory effects on large-scale brain network dynamics.SIGNIFICANCE STATEMENTThe catecholamines norepinephrine and dopamine are an important class of modulatory neurotransmitters. Because of the widespread and diffuse release of these neuromodulators, it has commonly been assumed that their effects on neural interactions are homogenous across the brain. Here, we present results from the human brain that challenge this view. We pharmacologically increased catecholamine levels and imaged the effects on the spontaneous covariations between brain-wide fMRI signals at ‘rest’. We identified two distinct spatial patterns of covariations: one that was amplified and another that was suppressed by catecholamines. Each pattern was associated with the heterogeneous spatial distribution of the expression of distinct catecholamine receptor genes. Our results provide novel insights into the catecholaminergic modulation of large-scale human brain dynamics.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Ruedeerat Keerativittayayut ◽  
Ryuta Aoki ◽  
Mitra Taghizadeh Sarabi ◽  
Koji Jimura ◽  
Kiyoshi Nakahara

Although activation/deactivation of specific brain regions has been shown to be predictive of successful memory encoding, the relationship between time-varying large-scale brain networks and fluctuations of memory encoding performance remains unclear. Here, we investigated time-varying functional connectivity patterns across the human brain in periods of 30–40 s, which have recently been implicated in various cognitive functions. During functional magnetic resonance imaging, participants performed a memory encoding task, and their performance was assessed with a subsequent surprise memory test. A graph analysis of functional connectivity patterns revealed that increased integration of the subcortical, default-mode, salience, and visual subnetworks with other subnetworks is a hallmark of successful memory encoding. Moreover, multivariate analysis using the graph metrics of integration reliably classified the brain network states into the period of high (vs. low) memory encoding performance. Our findings suggest that a diverse set of brain systems dynamically interact to support successful memory encoding.


2020 ◽  
Vol 10 (1) ◽  
pp. 42 ◽  
Author(s):  
Luana Billeri ◽  
Serena Filoni ◽  
Emanuele Francesco Russo ◽  
Simona Portaro ◽  
David Militi ◽  
...  

The differential diagnosis of patients with Disorder of Consciousness (DoC), in particular in the chronic phase, is significantly difficult. Actually, about 40% of patients with unresponsive wakefulness syndrome (UWS) and the minimally conscious state (MCS) are misdiagnosed. Indeed, only advanced paraclinical approaches, including advanced EEG analyses, can allow achieving a more reliable diagnosis, that is, discovering residual traces of awareness in patients with UWS (namely, functional Locked-In Syndrome (fLIS)). These approaches aim at capturing the residual brain network models, at rest or that may be activated in response to relevant stimuli, which may be appropriate for awareness to emerge (despite their insufficiency to generate purposeful motor behaviors). For this, different brain network models have been studied in patients with DoC by using sensory stimuli (i.e., passive tasks), probing response to commands (i.e., active tasks), and during resting-state. Since it can be difficult for patients with DoC to perform even simple active tasks, this scoping review aims at summarizing the current, innovative neurophysiological examination methods in resting state/passive modality to differentiate and prognosticate patients with DoC. We conclude that the electrophysiologically-based diagnostic procedures represent an important resource for diagnosis, prognosis, and, therefore, management of patients with DoC, using advance passive and resting state paradigm analyses for the patients who lie in the “greyzones” between MCS, UWS, and fLIS.


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