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Tom Tetzlaff
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Journal Articles
Publisher: Journals Gateway
Neural Computation (2008) 20 (9): 2133–2184.
Published: 01 September 2008
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Correlated neural activity has been observed at various signal levels (e.g., spike count, membrane potential, local field potential, EEG, fMRI BOLD). Most of these signals can be considered as superpositions of spike trains filtered by components of the neural system (synapses, membranes) and the measurement process. It is largely unknown how the spike train correlation structure is altered by this filtering and what the consequences for the dynamics of the system and for the interpretation of measured correlations are. In this study, we focus on linearly filtered spike trains and particularly consider correlations caused by overlapping presynaptic neuron populations. We demonstrate that correlation functions and statistical second-order measures like the variance, the covariance, and the correlation coefficient generally exhibit a complex dependence on the filter properties and the statistics of the presynaptic spike trains. We point out that both contributions can play a significant role in modulating the interaction strength between neurons or neuron populations. In many applications, the coherence allows a filter-independent quantification of correlated activity. In different network models, we discuss the estimation of network connectivity from the high-frequency coherence of simultaneous intracellular recordings of pairs of neurons.
Journal Articles
Publisher: Journals Gateway
Neural Computation (2008) 20 (9): 2185–2226.
Published: 01 September 2008
Abstract
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The function of cortical networks depends on the collective interplay between neurons and neuronal populations, which is reflected in the correlation of signals that can be recorded at different levels. To correctly interpret these observations it is important to understand the origin of neuronal correlations. Here we study how cells in large recurrent networks of excitatory and inhibitory neurons interact and how the associated correlations affect stationary states of idle network activity. We demonstrate that the structure of the connectivity matrix of such networks induces considerable correlations between synaptic currents as well as between subthreshold membrane potentials, provided Dale's principle is respected. If, in contrast, synaptic weights are randomly distributed, input correlations can vanish, even for densely connected networks. Although correlations are strongly attenuated when proceeding from membrane potentials to action potentials (spikes), the resulting weak correlations in the spike output can cause substantial fluctuations in the population activity, even in highly diluted networks. We show that simple mean-field models that take the structure of the coupling matrix into account can adequately describe the power spectra of the population activity. The consequences of Dale's principle on correlations and rate fluctuations are discussed in the light of recent experimental findings.