13 research outputs found

    Modelling human choices: MADeM and decision‑making

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    Research supported by FAPESP 2015/50122-0 and DFG-GRTK 1740/2. RP and AR are also part of the Research, Innovation and Dissemination Center for Neuromathematics FAPESP grant (2013/07699-0). RP is supported by a FAPESP scholarship (2013/25667-8). ACR is partially supported by a CNPq fellowship (grant 306251/2014-0)

    25th annual computational neuroscience meeting: CNS-2016

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    The same neuron may play different functional roles in the neural circuits to which it belongs. For example, neurons in the Tritonia pedal ganglia may participate in variable phases of the swim motor rhythms [1]. While such neuronal functional variability is likely to play a major role the delivery of the functionality of neural systems, it is difficult to study it in most nervous systems. We work on the pyloric rhythm network of the crustacean stomatogastric ganglion (STG) [2]. Typically network models of the STG treat neurons of the same functional type as a single model neuron (e.g. PD neurons), assuming the same conductance parameters for these neurons and implying their synchronous firing [3, 4]. However, simultaneous recording of PD neurons shows differences between the timings of spikes of these neurons. This may indicate functional variability of these neurons. Here we modelled separately the two PD neurons of the STG in a multi-neuron model of the pyloric network. Our neuron models comply with known correlations between conductance parameters of ionic currents. Our results reproduce the experimental finding of increasing spike time distance between spikes originating from the two model PD neurons during their synchronised burst phase. The PD neuron with the larger calcium conductance generates its spikes before the other PD neuron. Larger potassium conductance values in the follower neuron imply longer delays between spikes, see Fig. 17.Neuromodulators change the conductance parameters of neurons and maintain the ratios of these parameters [5]. Our results show that such changes may shift the individual contribution of two PD neurons to the PD-phase of the pyloric rhythm altering their functionality within this rhythm. Our work paves the way towards an accessible experimental and computational framework for the analysis of the mechanisms and impact of functional variability of neurons within the neural circuits to which they belong

    Spatio-temporal dynamics of human fMRI resting rate

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    Spontaneous brain activity, measured under the absence of any overt task, has been investigated under the label of “resting state” for about 20 years with rising interest. While it was known since the beginnings of modern electrophysiology that the brain exhibits spontaneous fluctuations also during rest, the discovery, in 1995, that these fluctuations possess a robust spatio-temporal structure had a profound impact on how we understand and investigate brain activity. In this dissertation, we characterize the spatio-temporal dynamics of resting state on a macroscopic level using fMRI recordings from humans and combining novel data analysis tools with theoretical models on the level of the whole brain. We demonstrate the presence of common patterns of functional connectivity, known as resting state networks (RSNs), that evolve in time in both empirical and model data. We show that spontaneous fluctuations and their statistics are determined by the structure of the brain network and its dynamics.La actividad cerebral espontánea, o actividad de reposo, es aquella que uno puede registrar cuando el cerebro no está involucrado en ninguna tarea impuesta del exterior (tal como sería la presentación de un estímulo). El estudio de la actividad de reposo ha conocido un interés creciente durante los últimos 20 años. Si bien las fluctuaciones en la actividad de reposo eran conocidas desde los inicios de la electrofisiología moderna, el descubrimiento, en 1995, de que estas fluctuaciones muestran patrones espaciotemporales robustos ha tenido un impacto profundo en la manera de entender e investigar la actividad del cerebro. En esta disertación caracterizamos la dinámica espaciotemporal de la actividad de reposo a nivel macroscópico usando registros de fMRI en humanos y combinando nuevas herramientas de análisis y modelos teóricos del cerebro a gran escala. Observamos patrones comunes de conectividad funcional evolviendo en el tiempo tanto en los datos empíricos como en las simulaciones. Demostramos que las fluctuaciones de reposo y su estadística son determinadas por la estructura de la red cerebral y su dinámica

    Computational Models in Electroencephalography.

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    Resting state networks in empirical and simulated dynamic functional connectivity

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    It is well-established that patterns of functional connectivity (FC) - measures of correlated activity between pairs of voxels or regions observed in the human brain using neuroimaging - are robustly expressed in spontaneous activity during rest. These patterns are not static, but exhibit complex spatio-temporal dynamics. Over the last years, a multitude of methods have been proposed to reveal these dynamics on the level of the whole brain. One finding is that the brain transitions through different FC configurations over time, and substantial effort has been put into characterizing these configurations. However, the dynamics governing these transitions are more elusive, specifically, the contribution of stationary vs. non-stationary dynamics is an active field of inquiry. In this study, we use a whole-brain approach, considering FC dynamics between 66 ROIs covering the entire cortex. We combine an innovative dimensionality reduction technique, tensor decomposition, with a mean field model which possesses stationary dynamics. It has been shown to explain resting state FC averaged over time and multiple subjects, however, this average FC summarizes the spatial distribution of correlations while hiding their temporal dynamics. First, we apply tensor decomposition to resting state scans from 24 healthy controls in order to characterize spatio-temporal dynamics present in the data. We simultaneously utilize temporal and spatial information by creating tensors that are subsequently decomposed into sets of brain regions (“communities”) that share similar temporal dynamics, and their associated time courses. The tensors contain pairwise FC computed inside of overlapping sliding windows. Communities are discovered by clustering features pooled from all subjects, thereby ensuring that they generalize. We find that, on the group level, the data give rise to four distinct communities that resemble known resting state networks (RSNs): default mode network, visual network, control networks, and somatomotor network. Second, we simulate data with our stationary mean field model whose nodes are connected according to results from DTI and fiber tracking. In this model, all spatio-temporal structure is due to noisy fluctuations around the average FC. We analyze the simulated data in the same way as the empirical data in order to determine whether stationary dynamics can explain the emergence of distinct FC patterns (RSNs) which have their own time courses. We find that this is the case for all four networks using the spatio-temporal information revealed by tensor decomposition if nodes in the simulation are connected according to model-based effective connectivity. Furthermore, we find that these results require only a small part of the FC values, namely the highest values that occur across time and ROI pair. Our findings show that stationary dynamics can account for the emergence of RSNs. We provide an innovative method that does not make strong assumptions about the underlying data and is generally applicable to resting state or task data from different subject populations.This work was supported by the European Union, FP7 Marie Curie ITN “INDIREA” (Grant N. 606901; KG), FP7 FET ICT Flagship Human Brain Project (Grant N. 604102; MG), ERC Advanced Human Brain Project (Grant N. 604102; GD), European Union Horizon2020 (ERC Consolidator grant BrainModes 683049; PR); the Spanish Ministry for Economy, Industry and Competitiveness (MINECO) project “PIRE-PICCS” (Grant N. PCIN-2015-079; KG), SEMAINE ERA-Net NEURON Project (Grant N. PCIN2013-026; APA), and ICoBAM (Grant N. PSI2013-42091-P; GD); the James S. McDonnell Foundation (Brain Network Recovery Group, Grant N. JSMF22002082; PR); the German Ministry of Education and Research (Grant N. 01GQ1504A and 01GQ0971-5; PR); the Max-Planck Society (Minerva Program; PR)

    Resting state networks in empirical and simulated dynamic functional connectivity

    No full text
    It is well-established that patterns of functional connectivity (FC) - measures of correlated activity between pairs of voxels or regions observed in the human brain using neuroimaging - are robustly expressed in spontaneous activity during rest. These patterns are not static, but exhibit complex spatio-temporal dynamics. Over the last years, a multitude of methods have been proposed to reveal these dynamics on the level of the whole brain. One finding is that the brain transitions through different FC configurations over time, and substantial effort has been put into characterizing these configurations. However, the dynamics governing these transitions are more elusive, specifically, the contribution of stationary vs. non-stationary dynamics is an active field of inquiry. In this study, we use a whole-brain approach, considering FC dynamics between 66 ROIs covering the entire cortex. We combine an innovative dimensionality reduction technique, tensor decomposition, with a mean field model which possesses stationary dynamics. It has been shown to explain resting state FC averaged over time and multiple subjects, however, this average FC summarizes the spatial distribution of correlations while hiding their temporal dynamics. First, we apply tensor decomposition to resting state scans from 24 healthy controls in order to characterize spatio-temporal dynamics present in the data. We simultaneously utilize temporal and spatial information by creating tensors that are subsequently decomposed into sets of brain regions (“communities”) that share similar temporal dynamics, and their associated time courses. The tensors contain pairwise FC computed inside of overlapping sliding windows. Communities are discovered by clustering features pooled from all subjects, thereby ensuring that they generalize. We find that, on the group level, the data give rise to four distinct communities that resemble known resting state networks (RSNs): default mode network, visual network, control networks, and somatomotor network. Second, we simulate data with our stationary mean field model whose nodes are connected according to results from DTI and fiber tracking. In this model, all spatio-temporal structure is due to noisy fluctuations around the average FC. We analyze the simulated data in the same way as the empirical data in order to determine whether stationary dynamics can explain the emergence of distinct FC patterns (RSNs) which have their own time courses. We find that this is the case for all four networks using the spatio-temporal information revealed by tensor decomposition if nodes in the simulation are connected according to model-based effective connectivity. Furthermore, we find that these results require only a small part of the FC values, namely the highest values that occur across time and ROI pair. Our findings show that stationary dynamics can account for the emergence of RSNs. We provide an innovative method that does not make strong assumptions about the underlying data and is generally applicable to resting state or task data from different subject populations.This work was supported by the European Union, FP7 Marie Curie ITN “INDIREA” (Grant N. 606901; KG), FP7 FET ICT Flagship Human Brain Project (Grant N. 604102; MG), ERC Advanced Human Brain Project (Grant N. 604102; GD), European Union Horizon2020 (ERC Consolidator grant BrainModes 683049; PR); the Spanish Ministry for Economy, Industry and Competitiveness (MINECO) project “PIRE-PICCS” (Grant N. PCIN-2015-079; KG), SEMAINE ERA-Net NEURON Project (Grant N. PCIN2013-026; APA), and ICoBAM (Grant N. PSI2013-42091-P; GD); the James S. McDonnell Foundation (Brain Network Recovery Group, Grant N. JSMF22002082; PR); the German Ministry of Education and Research (Grant N. 01GQ1504A and 01GQ0971-5; PR); the Max-Planck Society (Minerva Program; PR)

    Functional harmonics reveal multi-dimensional basis functions underlying cortical organization

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    The human brain consists of specialized areas that flexibly interact to form a multitude of functional networks. Complementary to this notion of modular organization, brain function has been shown to vary along a smooth continuum across the whole cortex. We demonstrate a mathematical framework that accounts for both of these perspectives: harmonic modes. We calculate the harmonic modes of the brain’s functional connectivity graph, called ‘‘functional harmonics,’’ revealing a multi-dimensional, frequency-ordered set of basis functions. Functional harmonics link characteristics of cortical organization across several spatial scales, capturing aspects of intra-areal organizational features (retinotopy, somatotopy), delineating brain areas, and explaining macroscopic functional networks as well as global cortical gradients. Furthermore, we show how the activity patterns elicited by seven different tasks are reconstructed from a very small subset of functional harmonics. Our results suggest that the principle of harmonicity, ubiquitous in nature, also underlies functional cortical organization in the human brain.K.G. and P.H. are supported by Swiss National Science Foundation (170873). M.L.K. is supported by the Center for Music in the Brain funded by the Danish National Research Foundation (DNRF117), and Centre for Eudaimonia and Human Flourishing funded by the Pettit and Carlsberg Foundations. G.D. is supported Spanish National Research Project (PID2019-105772GB-I00 MCIU AEI) funded by the Spanish Ministry of Science, Innovation and Universities (MCIU), State Research Agency (AEI); the Human Brain Project Specific Grant Agreement 3 (HBP SGA3) (945539) funded by the EU H2020 FET Flagship programme; the SGR Research Support Group (2017 SGR 1545) funded by the Catalan Agency for Management of University and Research Grants (AGAUR); Neurotwin Digital twins for model-driven non-invasive electrical brain stimulation (101017716) funded by the EU H2020 FET Proactive programme; European School of Network Neuroscience (860563) funded by the EU H2020 MSCA-ITN Innovative Training Networks; CECH The Emerging Human Brain Cluster (001-P-001682) within the framework of the European Research Development Fund Operational Program of Catalonia 2014-2020; Brain-Connects: Brain Connectivity during Stroke Recovery and Rehabilitation (201725.33) funded by the Fundacio La Marato TV3; and Corticity, FLAG-ERA JTC 2017 (PCI2018-092891) funded by the Spanish Ministry of Science, Innovation and Universities (MCIU), State Research Agency (AEI). J.P. is supported by Australian NHMRC (APP1024800, APP1046198, and APP1085404), a Career Development Fellowship (APP1049596), and an ARC discovery project (DP140101560). S.A. is supported by the ERC (CAREGIVING 615539)

    The connectome spectrum as a canonical basis for a sparse representation of fast brain activity

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    The functional organization of neural processes is constrained by the brain's intrinsic structural connectivity, i.e., the connectome. Here, we explore how structural connectivity can improve the representation of brain activity signals and their dynamics. Using a multi-modal imaging dataset (electroencephalography, structural MRI, and diffusion MRI), we represent electrical brain activity at the cortical surface as a time-varying composition of harmonic modes of structural connectivity. These harmonic modes are known as connectome harmonics. Here we describe brain activity signal as a time-varying combination of connectome harmonics. We term this description as the connectome spectrum of the signal. We found that: first, the brain activity signal is represented more compactly by the connectome spectrum than by the traditional area-based representation; second, the connectome spectrum characterizes fast brain dynamics in terms of signal broadcasting profile, revealing different temporal regimes of integration and segregation that are consistent across participants. And last, the connectome spectrum characterizes fast brain dynamics with fewer degrees of freedom than area-based signal representations. Specifically, we show that a smaller number of dimensions capture the differences between low-level and high-level visual processing in the connectome spectrum. Also, we demonstrate that connectome harmonics capture more sensitively the topological properties of brain activity. In summary, this work provides statistical, functional, and topological evidence indicating that the description of brain activity in terms of structural connectivity fosters a more comprehensive understanding of large-scale dynamic neural functioning

    Doctoral thesis recital (collaborative piano)

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    Brillance pour saxophone alto et piano (1974) / Ida Gotkovsky -- Sonata for Piano and Cello in A Major Op. 69 (1809) / Ludwig van Beethoven -- Carmen Fantasy (1994) / Alexander RosenblattMusicSupervisor not listed on recital program
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