13 research outputs found

    Neural Interactome: Interactive Simulation of a Neuronal System

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    Connectivity and biophysical processes determine the functionality of neuronal networks. We, therefore, developed a real-time framework, called Neural Interactome1,2, to simultaneously visualize and interact with the structure and dynamics of such networks. Neural Interactome is a cross-platform framework, which combines graph visualization with the simulation of neural dynamics, or experimentally recorded multi neural time series, to allow application of stimuli to neurons to examine network responses. In addition, Neural Interactome supports structural changes, such as disconnection of neurons from the network (ablation feature). Neural dynamics can be explored on a single neuron level (using a zoom feature), back in time (using a review feature), and recorded (using presets feature). The development of the Neural Interactome was guided by generic concepts to be applicable to neuronal networks with different neural connectivity and dynamics. We implement the framework using a model of the nervous system of Caenorhabditis elegans (C. elegans) nematode, a model organism with resolved connectome and neural dynamics. We show that Neural Interactome assists in studying neural response patterns associated with locomotion and other stimuli. In particular, we demonstrate how stimulation and ablation help in identifying neurons that shape particular dynamics. We examine scenarios that were experimentally studied, such as touch response circuit, and explore new scenarios that did not undergo elaborate experimental studies

    27th Annual Computational Neuroscience Meeting (CNS*2018): Part One

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    29th Annual Computational Neuroscience Meeting: CNS*2020

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    Meeting abstracts This publication was funded by OCNS. The Supplement Editors declare that they have no competing interests. Virtual | 18-22 July 202

    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

    25th Annual Computational Neuroscience Meeting: CNS-2016

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    Abstracts of the 25th Annual Computational Neuroscience Meeting: CNS-2016 Seogwipo City, Jeju-do, South Korea. 2–7 July 201

    Neuron-Glial Interactions

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    Although lagging behind classical computational neuroscience, theoretical and computational approaches are beginning to emerge to characterize different aspects of neuron-glial interactions. This chapter aims to provide essential knowledge on neuron-glial interactions in the mammalian brain, leveraging on computational studies that focus on structure (anatomy) and function (physiology) of such interactions in the healthy brain. Although our understanding of the need of neuron-glial interactions in the brain is still at its infancy, being mostly based on predictions that await for experimental validation, simple general modeling arguments borrowed from control theory are introduced to support the importance of including such interactions in traditional neuron-based modeling paradigms.Comment: 43 pages, 2 figures, 1 table. Accepted for publication in the "Encyclopedia of Computational Neuroscience," D. Jaeger and R. Jung eds., Springer-Verlag New York, 2020 (2nd edition

    Dynamics meets Morphology: towards Dymorph Computation

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    In this dissertation, approaches are presented for both technically using and investigating biological principles with oscillators in the context of electrical engineering, in particular neuromorphic engineering. Thereby, dynamics as well as morphology as important neuronal principles were explicitly selected, which shape the information processing in the human brain and distinguish it from other technical systems. The aspects and principles selected here are adaptation during the encoding of stimuli, the comparatively low signal transmission speed, the continuous formation and elimination of connections, and highly complex, partly chaotic, dynamics. The selection of these phenomena and properties has led to the development of a sensory unit that is capable of encoding mechanical stress into a series of voltage pulses by the use of a MOSFET augmented by AlScN. The circuit is based on a leaky integrate and fire neuron model and features an adaptation of the pulse frequency. Furthermore, the slow signal transmission speed of biological systems was the motivation for the investigation of a temporal delay in the feedback of the output pulses of a relaxation oscillator. In this system stable pulse patterns which form due to so-called jittering bifurcations could be observed. In particular, switching between different stable pulse patterns was possible to induce. In the further course of the work, the first steps towards time-varying coupling of dynamic systems are investigated. It was shown that in a system consisting of dimethyl sulfoxid and zinc acetate, oscillators can be used to force the formation of filaments. The resulting filaments then lead to a change in the dynamics of the oscillators. Finally, it is shown that in a system with chaotic dynamics, the extension of it with a memristive device can lead to a transient stabilisation of the dynamics, a behaviour that can be identified as a repeated pass of Hopf bifurcations

    Noise, coherent activity and network structure in neuronal cultures

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    In this thesis we apply a multidisciplinary approach, based on statistical physics and complex systems, to the study of neuronal dynamics. We focus on understanding, using theoretical and computational tools, how collective neuronal activity emerges in a controlled system, a neuronal culture. We show how the interplay between noise and network structure defines the emergent collective behavior of the system. We build, using theory and simulation, a framework that takes carefully describes spontaneous activity in neuronal cultures by taking into account the underlying network structure of neuronal cultures and use an accurate, yet simple, model for the individual neuronal dynamics. We show that the collective behavior of young cultures is dominated by the nucleation and propagations of activity fronts (bursts) throughout the system. These bursts nucleate at specific sites of the culture, called nucleation points, which result in a highly heterogeneous probability distribution of nucleation. We are able to explain the nucleation mechanism theoretically as a mechanism of noise propagation and amplification called noise focusing. We also explore the internal structure of activity avalanches by using well--defined regular networks, in which all the neurons have the same connectivity rules (motifs). Within these networks, we are able to associate to the avalanches an effective velocity and topological size and relate it to specific motifs. We also devise a continuum description of a neuronal culture at the mesoscale, i.e., we move away from the single neuron dynamics into a coarse--grained description that is able to capture most of the characteristic observables presented in previous chapters. This thesis also studies the spontaneous activity of neuronal cultures within the framework of quorum percolation. We study the effect of network structure within quorum percolation and propose a new model, called stochastic quorum percolation, that includes dynamics and the effect of internal noise. Finally, we use tools from information theory, namely transfer entropy, to show how to reliably infer the connectivity of a neuronal network from its activity, and how to distinguish between different excitatory and inhibitory connections purely from the activity, with no prior knowledge of the different neuronal types. The technique works directly on the fluorescence traces obtained in calcium imaging experiments, without the need to infer the underlying spike trains
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