53,804 research outputs found
The Impact Of Spike-Frequency Adaptation On Balanced Network Dynamics
A dynamic balance between strong excitatory and inhibitory neuronal inputs is hypothesized to play a pivotal role in information processing in the brain. While there is evidence of the existence of a balanced operating regime in several cortical areas and idealized neuronal network models, it is important for the theory of balanced networks to be reconciled with more physiological neuronal modeling assumptions. In this work, we examine the impact of spike-frequency adaptation, observed widely across neurons in the brain, on balanced dynamics. We incorporate adaptation into binary and integrate-and-fire neuronal network models, analyzing the theoretical effect of adaptation in the large network limit and performing an extensive numerical investigation of the model adaptation parameter space. Our analysis demonstrates that balance is well preserved for moderate adaptation strength even if the entire network exhibits adaptation. In the common physiological case in which only excitatory neurons undergo adaptation, we show that the balanced operating regime in fact widens relative to the non-adaptive case. We hypothesize that spike-frequency adaptation may have been selected through evolution to robustly facilitate balanced dynamics across diverse cognitive operating states
Regulation of Irregular Neuronal Firing by Autaptic Transmission
The importance of self-feedback autaptic transmission in modulating
spike-time irregularity is still poorly understood. By using a biophysical
model that incorporates autaptic coupling, we here show that self-innervation
of neurons participates in the modulation of irregular neuronal firing,
primarily by regulating the occurrence frequency of burst firing. In
particular, we find that both excitatory and electrical autapses increase the
occurrence of burst firing, thus reducing neuronal firing regularity. In
contrast, inhibitory autapses suppress burst firing and therefore tend to
improve the regularity of neuronal firing. Importantly, we show that these
findings are independent of the firing properties of individual neurons, and as
such can be observed for neurons operating in different modes. Our results
provide an insightful mechanistic understanding of how different types of
autapses shape irregular firing at the single-neuron level, and they highlight
the functional importance of autaptic self-innervation in taming and modulating
neurodynamics.Comment: 27 pages, 8 figure
The impact of spike timing variability on the signal-encoding performance of neural spiking models
It remains unclear whether the variability of neuronal spike trains in vivo arises due to biological noise sources or represents highly precise encoding of temporally varying synaptic input signals. Determining the variability of spike timing can provide fundamental insights into the nature of strategies used in the brain to represent and transmit information in the form of discrete spike trains. In this study, we employ a signal estimation paradigm to determine how variability in spike timing affects encoding of random time-varying signals. We assess this for two types of spiking models: an integrate-and-fire model with random threshold and a more biophysically realistic stochastic ion channel model. Using the coding fraction and mutual information as information-theoretic measures, we quantify the efficacy of optimal linear decoding of random inputs from the model outputs and study the relationship between efficacy and variability in the output spike train. Our findings suggest that variability does not necessarily hinder signal decoding for the biophysically plausible encoders examined and that the functional role of spiking variability depends intimately on the nature of the encoder and the signal processing task; variability can either enhance or impede decoding performance
Neuronal Synchronization Can Control the Energy Efficiency of Inter-Spike Interval Coding
The role of synchronous firing in sensory coding and cognition remains
controversial. While studies, focusing on its mechanistic consequences in
attentional tasks, suggest that synchronization dynamically boosts sensory
processing, others failed to find significant synchronization levels in such
tasks. We attempt to understand both lines of evidence within a coherent
theoretical framework. We conceptualize synchronization as an independent
control parameter to study how the postsynaptic neuron transmits the average
firing activity of a presynaptic population, in the presence of
synchronization. We apply the Berger-Levy theory of energy efficient
information transmission to interpret simulations of a Hodgkin-Huxley-type
postsynaptic neuron model, where we varied the firing rate and synchronization
level in the presynaptic population independently. We find that for a fixed
presynaptic firing rate the simulated postsynaptic interspike interval
distribution depends on the synchronization level and is well-described by a
generalized extreme value distribution. For synchronization levels of 15% to
50%, we find that the optimal distribution of presynaptic firing rate,
maximizing the mutual information per unit cost, is maximized at ~30%
synchronization level. These results suggest that the statistics and energy
efficiency of neuronal communication channels, through which the input rate is
communicated, can be dynamically adapted by the synchronization level.Comment: 47 pages, 14 figures, 2 Table
Who is that? Brain networks and mechanisms for identifying individuals
Social animals can identify conspecifics by many forms of sensory input. However, whether the neuronal computations that support this ability to identify individuals rely on modality-independent convergence or involve ongoing synergistic interactions along the multiple sensory streams remains controversial. Direct neuronal measurements at relevant brain sites could address such questions, but this requires better bridging the work in humans and animal models. Here, we overview recent studies in nonhuman primates on voice and face identity-sensitive pathways and evaluate the correspondences to relevant findings in humans. This synthesis provides insights into converging sensory streams in the primate anterior temporal lobe (ATL) for identity processing. Furthermore, we advance a model and suggest how alternative neuronal mechanisms could be tested
Channel noise induced stochastic facilitation in an auditory brainstem neuron model
Neuronal membrane potentials fluctuate stochastically due to conductance
changes caused by random transitions between the open and close states of ion
channels. Although it has previously been shown that channel noise can
nontrivially affect neuronal dynamics, it is unknown whether ion-channel noise
is strong enough to act as a noise source for hypothesised noise-enhanced
information processing in real neuronal systems, i.e. 'stochastic
facilitation.' Here, we demonstrate that biophysical models of channel noise
can give rise to two kinds of recently discovered stochastic facilitation
effects in a Hodgkin-Huxley-like model of auditory brainstem neurons. The
first, known as slope-based stochastic resonance (SBSR), enables phasic neurons
to emit action potentials that can encode the slope of inputs that vary slowly
relative to key time-constants in the model. The second, known as inverse
stochastic resonance (ISR), occurs in tonically firing neurons when small
levels of noise inhibit tonic firing and replace it with burst-like dynamics.
Consistent with previous work, we conclude that channel noise can provide
significant variability in firing dynamics, even for large numbers of channels.
Moreover, our results show that possible associated computational benefits may
occur due to channel noise in neurons of the auditory brainstem. This holds
whether the firing dynamics in the model are phasic (SBSR can occur due to
channel noise) or tonic (ISR can occur due to channel noise).Comment: Published by Physical Review E, November 2013 (this version 17 pages
total - 10 text, 1 refs, 6 figures/tables); Associated matlab code is
available online in the ModelDB repository at
http://senselab.med.yale.edu/ModelDB/ShowModel.asp?model=15148
The Effect of synchronized inputs at the single neuron level
It is commonly assumed that temporal synchronization of excitatory synaptic inputs onto a single neuron increases its firing rate. We investigate here the role of synaptic synchronization for the leaky integrate-and-fire neuron as well as for a biophysically and anatomically detailed compartmental model of a cortical pyramidal cell. We find that if the number of excitatory inputs, N, is on the same order as the number of fully synchronized inputs necessary to trigger a single action potential, N_t, synchronization always increases the firing rate (for both constant and Poisson-distributed input). However, for large values of N compared to N_t, ''overcrowding'' occurs and temporal synchronization is detrimental to firing frequency. This behavior is caused by the conflicting influence of the low-pass nature of the passive dendritic membrane on the one hand and the refractory period on the other. If both temporal synchronization as well as the fraction of synchronized inputs (Murthy and Fetz 1993) is varied, synchronization is only advantageous if either N or the average input frequency, Æ’(in), are small enough
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