4,028 research outputs found
Representation of Time-Varying Stimuli by a Network Exhibiting Oscillations on a Faster Time Scale
Sensory processing is associated with gamma frequency oscillations (30–80 Hz) in sensory cortices. This raises the question whether gamma oscillations can be directly involved in the representation of time-varying stimuli, including stimuli whose time scale is longer than a gamma cycle. We are interested in the ability of the system to reliably distinguish different stimuli while being robust to stimulus variations such as uniform time-warp. We address this issue with a dynamical model of spiking neurons and study the response to an asymmetric sawtooth input current over a range of shape parameters. These parameters describe how fast the input current rises and falls in time. Our network consists of inhibitory and excitatory populations that are sufficient for generating oscillations in the gamma range. The oscillations period is about one-third of the stimulus duration. Embedded in this network is a subpopulation of excitatory cells that respond to the sawtooth stimulus and a subpopulation of cells that respond to an onset cue. The intrinsic gamma oscillations generate a temporally sparse code for the external stimuli. In this code, an excitatory cell may fire a single spike during a gamma cycle, depending on its tuning properties and on the temporal structure of the specific input; the identity of the stimulus is coded by the list of excitatory cells that fire during each cycle. We quantify the properties of this representation in a series of simulations and show that the sparseness of the code makes it robust to uniform warping of the time scale. We find that resetting of the oscillation phase at stimulus onset is important for a reliable representation of the stimulus and that there is a tradeoff between the resolution of the neural representation of the stimulus and robustness to time-warp.
Author Summary
Sensory processing of time-varying stimuli, such as speech, is associated with high-frequency oscillatory cortical activity, the functional significance of which is still unknown. One possibility is that the oscillations are part of a stimulus-encoding mechanism. Here, we investigate a computational model of such a mechanism, a spiking neuronal network whose intrinsic oscillations interact with external input (waveforms simulating short speech segments in a single acoustic frequency band) to encode stimuli that extend over a time interval longer than the oscillation's period. The network implements a temporally sparse encoding, whose robustness to time warping and neuronal noise we quantify. To our knowledge, this study is the first to demonstrate that a biophysically plausible model of oscillations occurring in the processing of auditory input may generate a representation of signals that span multiple oscillation cycles.National Science Foundation (DMS-0211505); Burroughs Wellcome Fund; U.S. Air Force Office of Scientific Researc
Nonlinear Hebbian learning as a unifying principle in receptive field formation
The development of sensory receptive fields has been modeled in the past by a
variety of models including normative models such as sparse coding or
independent component analysis and bottom-up models such as spike-timing
dependent plasticity or the Bienenstock-Cooper-Munro model of synaptic
plasticity. Here we show that the above variety of approaches can all be
unified into a single common principle, namely Nonlinear Hebbian Learning. When
Nonlinear Hebbian Learning is applied to natural images, receptive field shapes
were strongly constrained by the input statistics and preprocessing, but
exhibited only modest variation across different choices of nonlinearities in
neuron models or synaptic plasticity rules. Neither overcompleteness nor sparse
network activity are necessary for the development of localized receptive
fields. The analysis of alternative sensory modalities such as auditory models
or V2 development lead to the same conclusions. In all examples, receptive
fields can be predicted a priori by reformulating an abstract model as
nonlinear Hebbian learning. Thus nonlinear Hebbian learning and natural
statistics can account for many aspects of receptive field formation across
models and sensory modalities
Neural activity classification with machine learning models trained on interspike interval series data
The flow of information through the brain is reflected by the activity
patterns of neural cells. Indeed, these firing patterns are widely used as
input data to predictive models that relate stimuli and animal behavior to the
activity of a population of neurons. However, relatively little attention was
paid to single neuron spike trains as predictors of cell or network properties
in the brain. In this work, we introduce an approach to neuronal spike train
data mining which enables effective classification and clustering of neuron
types and network activity states based on single-cell spiking patterns. This
approach is centered around applying state-of-the-art time series
classification/clustering methods to sequences of interspike intervals recorded
from single neurons. We demonstrate good performance of these methods in tasks
involving classification of neuron type (e.g. excitatory vs. inhibitory cells)
and/or neural circuit activity state (e.g. awake vs. REM sleep vs. nonREM sleep
states) on an open-access cortical spiking activity dataset
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