An integral equation describing the time evolution of the population activity in a homogeneous pool of spiking neurons of the integrate-and-fire 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 integrate-and-fire 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.

Several formulations of correlation-based Hebbian learning are reviewed. On the presynaptic side, activity is described either by a firing rate or by presynaptic spike arrival. The state of the postsynaptic neuron can be described by its membrane potential, its firing rate, or the timing of backpropagating action potentials (BPAPs). It is shown that all of the above formulations can be derived from the point of view of an expansion. In the absence of BPAPs potentials, it is natural to correlate presynaptic spikes with the postsynaptic membrane potential. Time windows of spike time dependent plasticity arise naturally, if the timing of postsynaptic spikes is available at the site of the synapse as it is the case in the presence of BPAPs. With an appropriate choice of parameters, Hebbian synaptic plasticity has intrinsic normalization properties that stabilizes postsynaptic firing rates and leads to subtractive weight normalization.

We demonstrate that single-variable integrate-and-fire models can quantitatively capture the dynamics of a physiologically-detailed model for fast-spiking cortical neurons. Through a systematic set of approximations, we reduce the conductance based model to two variants of integrate-and-fire models. In the first variant (non-linear integrate-and-fire model), parameters depend on the instantaneous membrane potential whereas in the second variant, they depend on the time elapsed since the last spike (Spike Response Model). The direct reduction links features of the simple models to biophysical features of the full conductance based model. To quantitatively

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Abstract: Many biological neural network models face the problem of scalability because of the limited computational power of today’s computers. Thus, it is difficult to assess the efficiency of these models to solve complex problems such as image processing. Here, we describe how this problem can be tackled using event-driven computation. Only the neurons that emit a discharge are processed and, as long as the average spike discharge rate is low, millions of neurons and billions of connections can be modeled. We describe the underlying computation and implementation of such a mechanism in SpikeNET, our neural network simulation package. The type of model one can build is not only biologically compliant, it is also computationally efficient as 400 000 synaptic weights can be propagated per second on a standard desktop computer. In addition, for large networks, we can set very small time steps (less than 0.01 ms) without significantly increasing the computation time. As an example, this method is applied to solve complex cognitive tasks such as face recognition in natural images.

How does a neuron vary its mean output firing rate if the input changes from random to coherent activity? What are the critical parameters of the neuronal dynamics and input statistics? To answer these questions, we investigate the coincidence detection properties of an integrate-and-fire neuron. We derive an expression indicating how coincidence detection depends on neuronal parameters. Specifically, (i) we show how coincidence detection depends on the shape of the postsynaptic response function, the number of synapses, and the input statistics, and (ii) we demonstrate that there is an optimal threshold. Our considerations can be used to predict from neuronal parameters whether and to what extent a neuron can act as a coincidence detector and thus can convert a temporal code into a rate code. Physik-Department der TU Munchen (T35), D-85747 Garching bei Munchen, Germany y Swiss Federal Institute of Technology, Center of Neuromimetic Systems, EPFL-DI, CH-1015 Lausanne, Switz...

This paper is an in-depth review on silicon implementations of threshold logic gates that covers several decades. In this paper, we will mention early MOS threshold logic solutions and detail numerous very-large-scale integration (VLSI) implementations including capacitive (switched capacitor and floating gate with their variations), conductance/current (pseudo-nMOS and output-wired-inverters, including a plethora of solutions evolved from them), as well as many differential solutions. At the end, we will briefly mention other implementations, e.g., based on negative resistance devices and on single electron technologies.

INTRODUCTION Oscillations occur in many networks of neurons, and are associated with motor behavior, sensory processing, learning, arousal, attention and pathology (Parkinson's tremor, epilepsy). Such oscillations can be generated in many ways. This chapter discusses some mathematical issues associated with creation of coherent rhythmic activity in networks of neurons. We focus on pairs of cells, since many of the issues for larger networks are most clearly displayed in that context. As we will show, there are many mechanisms for interactions among the network components, and these can have different mathematical properties. A description of behavior of larger networks using some of the mechanisms described in this chapter can be found in the related chapter by Rubin and Terman. For reviews of papers about oscillatory behavior in specific networks in the nervous system, see Gray (1994), Marder and Calabrese (1996), Singer (1993), and Traub et al (1999). The chapter is organiz

We present a dynamical theory of integrate-and-fire neurons with strong synaptic coupling. We show how phase-locked states that are stable in the weak coupling regime can destabilize as the coupling is increased, leading to states characterized by spatiotemporal variations in the interspike intervals (ISIs). The dynamics is compared with that of a corresponding network of analog neurons in which the outputs of the neurons are taken to be mean firing rates. A fundamental result is that for slow interactions, there is good agreement between the two models (on an appropriately defined timescale). Various examples of desynchronization in the strong coupling regime are presented. First, a globally coupled network of identical neurons with strong inhibitory coupling is shown to exhibit oscillator death in which some of the neurons suppress the activity of others. However, the stability of the synchronous state persists for very large networks and fast synapses. Second, an asymmetric network with a mixture of excitation and inhibition is shown to exhibit periodic bursting patterns. Finally, a one-dimensional network of neurons with long-range interactions is shown to desynchronize to a state with a spatially periodic pattern of mean firing rates across the network. This is modulated by deterministic fluctuations of the instantaneous firing rate whose size is an increasing function of the speed of synaptic response. 1

A novel approach to cortical modeling was introduced by Knight et al. (1996). In their presentation cortical dynamics is formulated in terms of in- teracting populations of neurons, a perspective that is in part motivated by modern cortical imaging (For a review see Sirovich and Kaplan (2002)). The approach