859 research outputs found
Synchronization of coupled neural oscillators with heterogeneous delays
We investigate the effects of heterogeneous delays in the coupling of two
excitable neural systems. Depending upon the coupling strengths and the time
delays in the mutual and self-coupling, the compound system exhibits different
types of synchronized oscillations of variable period. We analyze this
synchronization based on the interplay of the different time delays and support
the numerical results by analytical findings. In addition, we elaborate on
bursting-like dynamics with two competing timescales on the basis of the
autocorrelation function.Comment: 18 pages, 14 figure
Shared inputs, entrainment, and desynchrony in elliptic bursters: from slow passage to discontinuous circle maps
What input signals will lead to synchrony vs. desynchrony in a group of
biological oscillators? This question connects with both classical dynamical
systems analyses of entrainment and phase locking and with emerging studies of
stimulation patterns for controlling neural network activity. Here, we focus on
the response of a population of uncoupled, elliptically bursting neurons to a
common pulsatile input. We extend a phase reduction from the literature to
capture inputs of varied strength, leading to a circle map with discontinuities
of various orders. In a combined analytical and numerical approach, we apply
our results to both a normal form model for elliptic bursting and to a
biophysically-based neuron model from the basal ganglia. We find that,
depending on the period and amplitude of inputs, the response can either appear
chaotic (with provably positive Lyaponov exponent for the associated circle
maps), or periodic with a broad range of phase-locked periods. Throughout, we
discuss the critical underlying mechanisms, including slow-passage effects
through Hopf bifurcation, the role and origin of discontinuities, and the
impact of noiseComment: 17 figures, 40 page
Gap junctions and emergent rhythms
Gap junction coupling is ubiquitous in the brain, particularly between the dendritic trees of inhibitory interneurons. Such direct non-synaptic interaction allows for direct electrical communication between cells. Unlike spike-time driven synaptic neural network models, which are event based, any model with gap junctions must necessarily involve a single neuron model that can represent the shape of an action potential. Indeed, not only do neurons communicating via gaps feel super-threshold spikes, but they also experience, and respond to, sub-threshold voltage signals. In this chapter we show that the so-called absolute integrate-and-fire model is ideally suited to such studies. At the single neuron level voltage traces for the model may be obtained in closed form, and are shown to mimic those of fast-spiking inhibitory neurons. Interestingly in the presence of a slow spike adaptation current the model is shown to support periodic bursting oscillations. For both tonic and bursting modes the phase response curve can be calculated in closed form. At the network level we focus on global gap junction coupling and show how to analyze the asynchronous firing state in large networks. Importantly, we are able to determine the emergence of non-trivial network rhythms due to strong coupling instabilities. To illustrate the use of our theoretical techniques (particularly the phase-density formalism used to determine stability) we focus on a spike adaptation induced transition from asynchronous tonic activity to synchronous bursting in a gap-junction coupled network
One-Dimensional Population Density Approaches to Recurrently Coupled Networks of Neurons with Noise
Mean-field systems have been previously derived for networks of coupled,
two-dimensional, integrate-and-fire neurons such as the Izhikevich, adapting
exponential (AdEx) and quartic integrate and fire (QIF), among others.
Unfortunately, the mean-field systems have a degree of frequency error and the
networks analyzed often do not include noise when there is adaptation. Here, we
derive a one-dimensional partial differential equation (PDE) approximation for
the marginal voltage density under a first order moment closure for coupled
networks of integrate-and-fire neurons with white noise inputs. The PDE has
substantially less frequency error than the mean-field system, and provides a
great deal more information, at the cost of analytical tractability. The
convergence properties of the mean-field system in the low noise limit are
elucidated. A novel method for the analysis of the stability of the
asynchronous tonic firing solution is also presented and implemented. Unlike
previous attempts at stability analysis with these network types, information
about the marginal densities of the adaptation variables is used. This method
can in principle be applied to other systems with nonlinear partial
differential equations.Comment: 26 Pages, 6 Figure
On the complex dynamics of intracellular ganglion cell light responses in the cat retina
We recorded intracellular responses from cat retinal ganglion cells to sinusoidal flickering lights and compared the response dynamics to a theoretical model based on coupled nonlinear oscillators. Flicker responses for several different spot sizes were separated in a 'smooth' generator (G) potential and eorresponding spike trains. We have previously shown that the G-potential reveals complex, stimulus dependent, oscillatory behavior in response to sinusoidally flickering lights. Such behavior could be simulated by a modified van der Pol oscillator. In this paper, we extend the model to account for spike generation as well, by including extended Hodgkin-Huxley equations describing local membrane properties.
We quantified spike responses by several parameters describing the mean and standard deviation of spike burst duration, timing (phase shift) of bursts, and the number of spikes in a burst. The dependence of these response parameters on stimulus frequency and spot size could be reproduced in great detail by coupling the van der Pol oscillator, and Hodgkin-Huxley equations. The model mimics many experimentally observed response patterns, including non-phase-locked irregular oscillations. Our findings suggest that the information in the ganglion cell spike train reflects both intraretinal processing, simulated by the van der Pol oscillator) and local membrane properties described by Hodgkin-Huxley equations. The interplay between these complex processes can be simulated by changing the coupling coefficients between the two oscillators. Our simulations therefore show that irregularities in spike trains, which normally are considered to be noise, may be interpreted as complex oscillations that might earry information.Whitehall Foundation (S93-24
Mechanisms explaining transitions between tonic and phasic firing in neuronal populations as predicted by a low dimensional firing rate model
Several firing patterns experimentally observed in neural populations have
been successfully correlated to animal behavior. Population bursting, hereby
regarded as a period of high firing rate followed by a period of quiescence, is
typically observed in groups of neurons during behavior. Biophysical
membrane-potential models of single cell bursting involve at least three
equations. Extending such models to study the collective behavior of neural
populations involves thousands of equations and can be very expensive
computationally. For this reason, low dimensional population models that
capture biophysical aspects of networks are needed.
\noindent The present paper uses a firing-rate model to study mechanisms that
trigger and stop transitions between tonic and phasic population firing. These
mechanisms are captured through a two-dimensional system, which can potentially
be extended to include interactions between different areas of the nervous
system with a small number of equations. The typical behavior of midbrain
dopaminergic neurons in the rodent is used as an example to illustrate and
interpret our results.
\noindent The model presented here can be used as a building block to study
interactions between networks of neurons. This theoretical approach may help
contextualize and understand the factors involved in regulating burst firing in
populations and how it may modulate distinct aspects of behavior.Comment: 25 pages (including references and appendices); 12 figures uploaded
as separate file
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