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227
Dynamics of Sparsely Connected Networks of Excitatory and Inhibitory Spiking Neurons
, 1999
"... The dynamics of networks of sparsely connected excitatory and inhibitory integrateand re neurons is studied analytically. The analysis reveals a very rich repertoire of states, including: Synchronous states in which neurons re regularly; Asynchronous states with stationary global activity and very ..."
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Cited by 306 (16 self)
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The dynamics of networks of sparsely connected excitatory and inhibitory integrateand re neurons is studied analytically. The analysis reveals a very rich repertoire of states, including: Synchronous states in which neurons re regularly; Asynchronous states with stationary global activity and very irregular individual cell activity; States in which the global activity oscillates but individual cells re irregularly, typically at rates lower than the global oscillation frequency. The network can switch between these states, provided the external frequency, or the balance between excitation and inhibition, is varied. Two types of network oscillations are observed: In the `fast' oscillatory state, the network frequency is almost fully controlled by the synaptic time scale. In the `slow' oscillatory state, the network frequency depends mostly on the membrane time constant. Finite size eects in the asynchronous state are also discussed.
Population Dynamics of Spiking Neurons: Fast Transients, Asynchronous States, and Locking
 NEURAL COMPUTATION
, 2000
"... An integral equation describing the time evolution of the population activity in a homogeneous pool of spiking neurons of the integrateandfire type is discussed. It is analytically shown that transients from a state of incoherent firing can be immediate. The stability of incoherent firing is analy ..."
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Cited by 159 (25 self)
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An integral equation describing the time evolution of the population activity in a homogeneous pool of spiking neurons of the integrateandfire type is discussed. It is analytically shown that transients from a state of incoherent firing can be immediate. The stability of incoherent firing is analyzed in terms of the noise level and transmission delay and a bifurcation diagram is derived. The response of a population of noisy integrateandfire neurons to an input current of small amplitude is calculated and characterized by a linear filter L. The stability of perfectly synchronized `locked' solutions is analyzed.
What determines the frequency of fast network oscillations with irregular neural discharges? I. Synaptic dynamics and excitationinhibition balance
 J NEUROPHYSIOL 90: 415–430, 2003
, 2003
"... When the local field potential of a cortical network displays coherent fast oscillations (~40Hz gamma or ~200Hz sharpwave ripples), the spike trains of constituent neurons are typically irregular and sparse. The dichotomy between rhythmic local field and stochastic spike trains presents a challe ..."
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Cited by 130 (7 self)
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When the local field potential of a cortical network displays coherent fast oscillations (~40Hz gamma or ~200Hz sharpwave ripples), the spike trains of constituent neurons are typically irregular and sparse. The dichotomy between rhythmic local field and stochastic spike trains presents a challenge to the theory of brain rhythms in the framework of coupled oscillators. Previous studies have shown that when noise is large and recurrent inhibition is strong, a coherent network rhythm can be generated while single neurons fire intermittently at low rates compared to the frequency of the oscillation. However, these studies used too simplified synaptic kinetics to allow quantitative predictions of the population rhythmic frequency. Here we show how to derive quantitatively the coherent
Effects of Neuromodulation in a Cortical Network Model of Object Working Memory Dominated by Recurrent Inhibition
 Journal of Computational Neuroscience
, 2001
"... Experimental evidence suggests that the maintenance of an item in working memory is achieved through persistent activity in selective neural assemblies of the cortex. To understand the mechanisms underlying this phenomenon, it is essential to investigate how persistent activity is affected by extern ..."
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Cited by 115 (5 self)
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Experimental evidence suggests that the maintenance of an item in working memory is achieved through persistent activity in selective neural assemblies of the cortex. To understand the mechanisms underlying this phenomenon, it is essential to investigate how persistent activity is affected by external inputs or neuromodulation. We have addressed these questions using a recurrent network model of object working memory. Recurrence is dominated by inhibition, although persistent activity is generated through recurrent excitation in small subsets of excitatory neurons.
Synchronization in networks of excitatory and inhibitory neurons with sparse, random connectivity
 Neural Computation
, 2003
"... In model networks of Ecells and Icells (excitatory and inhibitory neurons) , synchronous rhythmic spiking often comes about from the interplay between the two cell groups: the Ecells synchronize the Icells and vice versa. Under ideal conditions  homogeneity in relevant network parameters, ..."
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Cited by 74 (8 self)
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In model networks of Ecells and Icells (excitatory and inhibitory neurons) , synchronous rhythmic spiking often comes about from the interplay between the two cell groups: the Ecells synchronize the Icells and vice versa. Under ideal conditions  homogeneity in relevant network parameters, and alltoall connectivity for instance  this mechanism can yield perfect synchronization.
Collective Behavior of Networks with Linear (VLSI) IntegrateandFire Neurons
, 1999
"... Introduction The integrateandfire (IF) neuron has become popular as a simplified neural element in modeling the dynamics of largescale networks of spiking neurons. A simple version of an IF neuron integrates the input current as an RC circuit (with a leakage current proportional to the depolariz ..."
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Cited by 71 (22 self)
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Introduction The integrateandfire (IF) neuron has become popular as a simplified neural element in modeling the dynamics of largescale networks of spiking neurons. A simple version of an IF neuron integrates the input current as an RC circuit (with a leakage current proportional to the depolarization) and emits a spike when the depolarization crosses a threshold. We will refer to it as the RC neuron. Networks of neurons schematized in this way exhibit a wide variety of characteristics observed in single and multiple neuron recordings in cortex in vivo. With biologically plausible time constants and synaptic efficacies, they can maintain spontaneous activity, and when the network is subjected to Hebbian learning (subsets of cells are repeatedly activated by the external stimuli), it shows many stable states of activation, each corresponding to a different attractor of the network dynamics, in coexistence with spontaneous activity (Amit & Brunel, 1997a). These s
A population density approach that facilitates largescale modeling of neural networks: Analysis and an application to orientation tuning
 J. Comp. Neurosci
, 2000
"... We explore a computationally efficient method of simulating realistic networks of neurons introduced by Knight, Manin, and Sirovich (1996) in which integrateandfire neurons are grouped into large populations of similar neurons. For each population, we form a probability density which represents th ..."
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Cited by 61 (2 self)
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We explore a computationally efficient method of simulating realistic networks of neurons introduced by Knight, Manin, and Sirovich (1996) in which integrateandfire neurons are grouped into large populations of similar neurons. For each population, we form a probability density which represents the distribution of neurons over all possible states. The populations are coupled via stochastic synapses in which the conductance of a neuron is modulated according to the firing rates of its presynaptic populations. The evolution equation for each of these probability densities is a partial differentialintegral equation which we solve numerically. Results obtained for several example networks are tested against conventional computations for groups of individual neurons. We apply this approach to modeling orientation tuning in the visual cortex. Our population density model is based on the recurrent feedback model of a hypercolumn in cat visual cortex of Somers et al. (1995). We simulate the response to oriented flashed bars. As in the Somers model, a weak orientation bias provided by feedforward lateral geniculate input is transformed by intracortical circuitry into sharper orientation tuning which is independent of stimulus contrast. The population density approach appears to be a viable method for simulating large neural networks. Its computational efficiency overcomes some of the restrictions imposed by computation time in individual
Noise in IntegrateandFire Neurons: From Stochastic Input to Escape Rates
 TO APPEAR IN NEURAL COMPUTATION.
, 1999
"... We analyze the effect of noise in integrateandfire neurons driven by timedependent input, and compare the diffusion approximation for the membrane potential to escape noise. It is shown that for timedependent subthreshold input, diffusive noise can be replaced by escape noise with a hazard funct ..."
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Cited by 51 (6 self)
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We analyze the effect of noise in integrateandfire neurons driven by timedependent input, and compare the diffusion approximation for the membrane potential to escape noise. It is shown that for timedependent subthreshold input, diffusive noise can be replaced by escape noise with a hazard function that has a Gaussian dependence upon the distance between the (noisefree) membrane voltage and threshold. The approximation is improved if we add to the hazard function a probability current proportional to the derivative of the voltage. Stochastic resonance in response to periodic input occurs in both noise models and exhibits similar characteristics.
Firing Rate of the Noisy Quadratic IntegrateandFire Neuron
, 2003
"... We calculate the firing rate of the quadratic integrateandfire neuron in response to a colored noise input current. Such an input current is a good approximation to the noise due to the random bombardment of spikes, with the correlation time of the noise corresponding to the decay time of the syna ..."
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Cited by 46 (4 self)
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We calculate the firing rate of the quadratic integrateandfire neuron in response to a colored noise input current. Such an input current is a good approximation to the noise due to the random bombardment of spikes, with the correlation time of the noise corresponding to the decay time of the synapses. The key parameter that determines the firing rate is the ratio of the correlation time of the colored noise, ¿s, to the neuronal time constant, ¿m. We calculate the firing rate exactly in two limits: when the ratio, ¿s=¿m, goes to zero (white noise) and when it goes to infinity. The correction to the short correlation time limit is O.¿s=¿m/, which is qualitatively different from that of the leaky integrateandfire neuron, where the correction is O. p ¿s=¿m/. The difference is due to the different boundary conditions of the probability density function of the membrane potential of the neuron at firing threshold. The correction to the long correlation time limit is O.¿m=¿s/. By combining the short and long correlation time limits, we derive an expression that provides a good approximation to the firing rate over the whole range of ¿s=¿m in the suprathreshold regime— that is, in a regime in which the average current is sufficient to make the cell fire. In the subthreshold regime, the expression breaks down somewhat when ¿s becomes large compared to ¿m.