Computational techniques within the population density function (PDF) framework have provided time-saving alternatives to classical Monte Carlo simulations of neural network activity. Efficiency of the PDF method is lost as the underlying neuron model is made more realistic and the number of state variables increases. In a detailed theoretical and computational study, we elucidate strengths and weaknesses of dimension reduction by a particular moment closure method (Cai, Tao, Shelley, & McLaughlin, 2004; Cai, Tao, Rangan, & McLaughlin, 2006) as applied to integrate-and-fire neurons that receive excitatory synaptic input only. When the unitary postsynaptic conductance event has a single-exponential time course, the evolution equation for the PDF is a partial differential integral equation in two state variables, voltage and excitatory conductance. In the moment closure method, one approximates the conditional kth centered moment of excitatory conductance given voltage by the corresponding unconditioned moment. The result is a system of k coupled partial differential equations with one state variable, voltage, and k coupled ordinary differential equations. Moment closure at k = 2 works well, and at k = 3 works even better, in the regime of high dynamically varying synaptic input rates. Both closures break down at lower synaptic input rates. Phase-plane analysis of the k = 2 problem with typical parameters proves, and reveals why, no steady-state solutions exist below a synaptic input rate that gives a firing rate of 59 s(1) in the full 2D problem. Closure at k = 3 fails for similar reasons. Low firing-rate solutions can be obtained only with parameters for the amplitude or kinetics (or both) of the unitary postsynaptic conductance event that are on the edge of the physiological range. We conclude that this dimension-reduction method gives ill-posed problems for a wide range of physiological parameters, and we suggest future directions.
An outstanding problem in computational neuroscience is how to use population density function (PDF) methods to model neural networks with realistic synaptic kinetics in a computationally efficient manner. We explore an application of two-dimensional (2-D) PDF methods to simulating electrical activity in networks of excitatory integrate-and-fire neurons. We formulate a pair of coupled partial differential-integral equations describing the evolution of PDFs for neurons in non-refractory and refractory pools. The population firing rate is given by the total flux of probability across the threshold voltage. We use an operator-splitting method to reduce computation time. We report on speed and accuracy of PDF results and compare them to those from direct, Monte-Carlo simulations. We compute temporal frequency response functions for the transduction from the rate of postsynaptic input to population firing rate, and examine its dependence on background synaptic input rate. The behaviors in the1-D and 2-D cases--corresponding to instantaneous and non-instantaneous synaptic kinetics, respectively--differ markedly from those for a somewhat different transduction: from injected current input to population firing rate output (Brunel et al. 2001; Fourcaud & Brunel 2002). We extend our method by adding inhibitory input, consider a 3-D to 2-D dimension reduction method, demonstrate its limitations, and suggest directions for future study.
The response of neurons to external stimuli greatly depends on the intrinsic dynamics of the network. Here, the intrinsic dynamics are modeled as coupling and the external input is modeled as shared and unshared noise. We assume the neurons are repetitively firing action potentials (i.e., neural oscillators), are weakly and identically coupled, and the external noise is weak. Shared noise can induce bistability between the synchronous and anti-phase states even though the anti-phase state is the only stable state in the absence of noise. We study the Fokker-Planck equation of the system and perform an asymptotic reduction rho(0). The rho(0) solution is more computationally efficient than both the Monte Carlo simulations and the 2D Fokker-Planck solver, and agrees remarkably well with the full system with weak noise and weak coupling. With moderate noise and coupling, rho(0) is still qualitatively correct despite the small noise and coupling assumption in the asymptotic reduction. Our phase model accurately predicts the behavior of a realistic synaptically coupled Morris-Lecar system.
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