324 research outputs found
Macroscopic equations governing noisy spiking neuronal populations
At functional scales, cortical behavior results from the complex interplay of
a large number of excitable cells operating in noisy environments. Such systems
resist to mathematical analysis, and computational neurosciences have largely
relied on heuristic partial (and partially justified) macroscopic models, which
successfully reproduced a number of relevant phenomena. The relationship
between these macroscopic models and the spiking noisy dynamics of the
underlying cells has since then been a great endeavor. Based on recent
mean-field reductions for such spiking neurons, we present here {a principled
reduction of large biologically plausible neuronal networks to firing-rate
models, providing a rigorous} relationship between the macroscopic activity of
populations of spiking neurons and popular macroscopic models, under a few
assumptions (mainly linearity of the synapses). {The reduced model we derive
consists of simple, low-dimensional ordinary differential equations with}
parameters and {nonlinearities derived from} the underlying properties of the
cells, and in particular the noise level. {These simple reduced models are
shown to reproduce accurately the dynamics of large networks in numerical
simulations}. Appropriate parameters and functions are made available {online}
for different models of neurons: McKean, Fitzhugh-Nagumo and Hodgkin-Huxley
models
Mean Field description of and propagation of chaos in recurrent multipopulation networks of Hodgkin-Huxley and Fitzhugh-Nagumo neurons
We derive the mean-field equations arising as the limit of a network of
interacting spiking neurons, as the number of neurons goes to infinity. The
neurons belong to a fixed number of populations and are represented either by
the Hodgkin-Huxley model or by one of its simplified version, the
Fitzhugh-Nagumo model. The synapses between neurons are either electrical or
chemical. The network is assumed to be fully connected. The maximum
conductances vary randomly. Under the condition that all neurons initial
conditions are drawn independently from the same law that depends only on the
population they belong to, we prove that a propagation of chaos phenomenon
takes places, namely that in the mean-field limit, any finite number of neurons
become independent and, within each population, have the same probability
distribution. This probability distribution is solution of a set of implicit
equations, either nonlinear stochastic differential equations resembling the
McKean-Vlasov equations, or non-local partial differential equations resembling
the McKean-Vlasov-Fokker- Planck equations. We prove the well-posedness of
these equations, i.e. the existence and uniqueness of a solution. We also show
the results of some preliminary numerical experiments that indicate that the
mean-field equations are a good representation of the mean activity of a finite
size network, even for modest sizes. These experiment also indicate that the
McKean-Vlasov-Fokker- Planck equations may be a good way to understand the
mean-field dynamics through, e.g., a bifurcation analysis.Comment: 55 pages, 9 figure
The space-clamped Hodgkin-Huxley system with random synaptic input: inhibition of spiking by weak noise and analysis with moment equations
We consider a classical space-clamped Hodgkin-Huxley model neuron stimulated
by synaptic excitation and inhibition with conductances represented by
Ornstein-Uhlenbeck processes. Using numerical solutions of the stochastic model
system obtained by an Euler method, it is found that with excitation only there
is a critical value of the steady state excitatory conductance for repetitive
spiking without noise and for values of the conductance near the critical value
small noise has a powerfully inhibitory effect. For a given level of inhibition
there is also a critical value of the steady state excitatory conductance for
repetitive firing and it is demonstrated that noise either in the excitatory or
inhibitory processes or both can powerfully inhibit spiking. Furthermore, near
the critical value, inverse stochastic resonance was observed when noise was
present only in the inhibitory input process.
The system of 27 coupled deterministic differential equations for the
approximate first and second order moments of the 6-dimensional model is
derived. The moment differential equations are solved using Runge-Kutta methods
and the solutions are compared with the results obtained by simulation for
various sets of parameters including some with conductances obtained by
experiment on pyramidal cells of rat prefrontal cortex. The mean and variance
obtained from simulation are in good agreement when there is spiking induced by
strong stimulation and relatively small noise or when the voltage is
fluctuating at subthreshold levels. In the occasional spike mode sometimes
exhibited by spinal motoneurons and cortical pyramidal cells the assunptions
underlying the moment equation approach are not satisfied
Predicting and identifying signs of criticality near neuronal phase transition
This thesis examines the critical transitions between distinct neural states associated with the transition to neuron spiking and with the induction of anaesthesia. First, mathematical and electronic models of a single spiking neuron are investigated, focusing on stochastic subthreshold dynamics on close approach to spiking and to depolarisation-blocked quiescence (spiking death) transition points. Theoretical analysis of subthreshold neural behaviour then shifts to the anaesthetic-induced phase transition into unconsciousness using a mean-field model for interacting populations of excitatory and inhibitory neurons. The anaesthetic-induced changes are validated experimentally using published electrophysiological data recorded in anaesthetised rats. The criticality hypothesis associated with brain state change is examined using neuronal avalanches for experimentally recorded rat local field potential (LFP) data and mean-field pseudoLFP simulation data.
We compare three different implementations of the FitzHugh--Nagumo single spiking neuron model: a mathematical model by H. R. Wilson, an alternative due to Keener and Sneyd, and an op-amp based nonlinear oscillator circuit. Although all three models can produce nonlinear ``spiking" oscillations, our focus is on the altering characteristics of noise-induced fluctuations near spiking onset and death via Hopf bifurcation. We introduce small-amplitude white noise to enable a linearised stochastic analyses using Ornstein--Uhlenbeck theory to predict variance, power spectrum and correlation of voltage fluctuations during close approach to the critical point, identified as the point at which the real part of the dominant eigenvalue becomes zero. We validate the theoretical predictions with numerical simulations and show that the fluctuations exhibit critical slowing down divergences when approaching the critical point: power-law increases in the variance of the fluctuations simultaneous with prolongation of the system response.
We expand the study of stochastic behaviour to two spatial dimensions using the Waikato mean-field model operating near phase transition points controlled by the infusion or elimination of anaesthetic inhibition. Specifically, we investigate close approach to the critical point (CP), and to the points of loss of consciousness (LOC) and recovery of consciousness (ROC). We select the equilibrium states using anaesthetic inhibition and cortical excitation as control parameters, then analyse the voltage fluctuations evoked by small-amplitude spatiotemporal white noise. We predict the variance and power spectrum of voltage fluctuations near the marginally stable LOC and ROC transition points, then validate via numerical simulation. The results demonstrate a marked increase in voltage fluctuations and spectral power near transition points. This increased susceptibility to low-intensity white noise stimulation provides an early warning of impending phase transition.
Effects of anaesthetic agents on cortical activity are reflected in local field potentials (LFPs) by the variation of amplitude and frequency in voltage fluctuations. To explore these changes, we investigate LFPs acquired from published electrophysiological experiments of anaesthetised rats to extract amplitude distribution, variance and time-correlation statistics. The analysis is broadened by applying detrended fluctuation analysis (DFA) to detect long-range dependencies in the time-series, and we compare DFA results with power spectral density (PSD). We find that the DFA exponent increases with anaesthetic concentration, but is always close to 1.
The penultimate chapter investigates the evidence of criticality in anaesthetic induced phase-transitions using avalanche analysis. Rat LFP data reveal an avalanche power-law exponent close to , but this value depends on both the time-bin width chosen to separate the events and the \textit{z}-score threshold used to detect these events. Power-law behaviour is only evident at lower anaesthetic concentrations; at higher concentrations the avalanche size distribution fails to align with a power-law nature. Criticality behaviour is also indicated in the Waikato mean-field model for anaesthetic-induced phase-transition using avalanches detected from the pseudoLFP time-series, but only at the critical point (CP) and at the secondary phase-transition points of LOC and ROC.
In summary, this thesis unveils evidence of characteristic changes near phase transition points using computer-based mathematical modelling and electrophysiological data analysis. We find that noise-driven fluctuations become larger and persist for longer as the critical point is closely approached, with similar properties being seen not only in single-neuron and neural population models, but also in biological LFP signals. These results consistent with an increase of susceptibility to noise perturbations near phase transition point. Identification of neuronal avalanches in rat LFP data for low anaesthetic concentrations provides further support for the criticality hypothesis
Stochastic neural network dynamics: synchronisation and control
Biological brains exhibit many interesting and complex behaviours. Understanding of the mechanisms behind brain behaviours is critical for continuing advancement in fields of research such as artificial intelligence and medicine. In particular, synchronisation of neuronal firing is associated with both improvements to and degeneration of the brainâs performance; increased synchronisation can lead to enhanced information-processing or neurological disorders such as epilepsy and Parkinsonâs disease. As a result, it is desirable to research under which conditions synchronisation arises in neural networks and the possibility of controlling its prevalence. Stochastic ensembles of FitzHugh-Nagumo elements are used to model neural networks for numerical simulations and bifurcation analysis. The FitzHugh-Nagumo model is employed because of its realistic representation of the flow of sodium and potassium ions in addition to its advantageous property of allowing phase plane dynamics to be observed. Network characteristics such as connectivity, configuration and size are explored to determine their influences on global synchronisation generation in their respective systems. Oscillations in the mean-field are used to detect the presence of synchronisation over a range of coupling strength values. To ensure simulation efficiency, coupling strengths between neurons that are identical and fixed with time are investigated initially. Such networks where the interaction strengths are fixed are referred to as homogeneously coupled. The capacity of controlling and altering behaviours produced by homogeneously coupled networks is assessed through the application of weak and strong delayed feedback independently with various time delays. To imitate learning, the coupling strengths later deviate from one another and evolve with time in networks that are referred to as heterogeneously coupled. The intensity of coupling strength fluctuations and the rate at which coupling strengths converge to a desired mean value are studied to determine their impact upon synchronisation performance. The stochastic delay differential equations governing the numerically simulated networks are then converted into a finite set of deterministic cumulant equations by virtue of the Gaussian approximation method. Cumulant equations for maximal and sub-maximal connectivity are used to generate two-parameter bifurcation diagrams on the noise intensity and coupling strength plane, which provides qualitative agreement with numerical simulations. Analysis of artificial brain networks, in respect to biological brain networks, are discussed in light of recent research in sleep theor
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