3,693 research outputs found
Neuromorphic Learning towards Nano Second Precision
Temporal coding is one approach to representing information in spiking neural
networks. An example of its application is the location of sounds by barn owls
that requires especially precise temporal coding. Dependent upon the azimuthal
angle, the arrival times of sound signals are shifted between both ears. In
order to deter- mine these interaural time differences, the phase difference of
the signals is measured. We implemented this biologically inspired network on a
neuromorphic hardware system and demonstrate spike-timing dependent plasticity
on an analog, highly accelerated hardware substrate. Our neuromorphic
implementation enables the resolution of time differences of less than 50 ns.
On-chip Hebbian learning mechanisms select inputs from a pool of neurons which
code for the same sound frequency. Hence, noise caused by different synaptic
delays across these inputs is reduced. Furthermore, learning compensates for
variations on neuronal and synaptic parameters caused by device mismatch
intrinsic to the neuromorphic substrate.Comment: 7 pages, 7 figures, presented at IJCNN 2013 in Dallas, TX, USA. IJCNN
2013. Corrected version with updated STDP curves IJCNN 201
Retinal oscillations carry visual information to cortex
Thalamic relay cells fire action potentials that transmit information from
retina to cortex. The amount of information that spike trains encode is usually
estimated from the precision of spike timing with respect to the stimulus.
Sensory input, however, is only one factor that influences neural activity. For
example, intrinsic dynamics, such as oscillations of networks of neurons, also
modulate firing pattern. Here, we asked if retinal oscillations might help to
convey information to neurons downstream. Specifically, we made whole-cell
recordings from relay cells to reveal retinal inputs (EPSPs) and thalamic
outputs (spikes) and analyzed these events with information theory. Our results
show that thalamic spike trains operate as two multiplexed channels. One
channel, which occupies a low frequency band (<30 Hz), is encoded by average
firing rate with respect to the stimulus and carries information about local
changes in the image over time. The other operates in the gamma frequency band
(40-80 Hz) and is encoded by spike time relative to the retinal oscillations.
Because these oscillations involve extensive areas of the retina, it is likely
that the second channel transmits information about global features of the
visual scene. At times, the second channel conveyed even more information than
the first.Comment: 21 pages, 10 figures, submitted to Frontiers in Systems Neuroscienc
Enhancement of synchronization in a hybrid neural circuit by spike timing dependent plasticity
Synchronization of neural activity is fundamental for many functions of the brain. We demonstrate that spike-timing dependent plasticity (STDP) enhances synchronization (entrainment) in a hybrid circuit composed of a spike generator, a dynamic clamp emulating an excitatory plastic synapse, and a chemically isolated neuron from the Aplysia abdominal ganglion. Fixed-phase entrainment of the Aplysia neuron to the spike generator is possible for a much wider range of frequency ratios and is more precise and more robust with the plastic synapse than with a nonplastic synapse of comparable strength. Further analysis in a computational model of HodgkinHuxley-type neurons reveals the mechanism behind this significant enhancement in synchronization. The experimentally observed STDP plasticity curve appears to be designed to adjust synaptic strength to a value suitable for stable entrainment of the postsynaptic neuron. One functional role of STDP might therefore be to facilitate synchronization or entrainment of nonidentical neurons
Simulation of networks of spiking neurons: A review of tools and strategies
We review different aspects of the simulation of spiking neural networks. We
start by reviewing the different types of simulation strategies and algorithms
that are currently implemented. We next review the precision of those
simulation strategies, in particular in cases where plasticity depends on the
exact timing of the spikes. We overview different simulators and simulation
environments presently available (restricted to those freely available, open
source and documented). For each simulation tool, its advantages and pitfalls
are reviewed, with an aim to allow the reader to identify which simulator is
appropriate for a given task. Finally, we provide a series of benchmark
simulations of different types of networks of spiking neurons, including
Hodgkin-Huxley type, integrate-and-fire models, interacting with current-based
or conductance-based synapses, using clock-driven or event-driven integration
strategies. The same set of models are implemented on the different simulators,
and the codes are made available. The ultimate goal of this review is to
provide a resource to facilitate identifying the appropriate integration
strategy and simulation tool to use for a given modeling problem related to
spiking neural networks.Comment: 49 pages, 24 figures, 1 table; review article, Journal of
Computational Neuroscience, in press (2007
Correlation entropy of synaptic input-output dynamics
The responses of synapses in the neocortex show highly stochastic and
nonlinear behavior. The microscopic dynamics underlying this behavior, and its
computational consequences during natural patterns of synaptic input, are not
explained by conventional macroscopic models of deterministic ensemble mean
dynamics. Here, we introduce the correlation entropy of the synaptic
input-output map as a measure of synaptic reliability which explicitly includes
the microscopic dynamics. Applying this to experimental data, we find that
cortical synapses show a low-dimensional chaos driven by the natural input
pattern.Comment: 7 pages, 6 Figures (7 figure files
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
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
Multiple firing coherence resonances in excitatory and inhibitory coupled neurons
The impact of inhibitory and excitatory synapses in delay-coupled
Hodgkin--Huxley neurons that are driven by noise is studied. If both synaptic
types are used for coupling, appropriately tuned delays in the inhibition
feedback induce multiple firing coherence resonances at sufficiently strong
coupling strengths, thus giving rise to tongues of coherency in the
corresponding delay-strength parameter plane. If only inhibitory synapses are
used, however, appropriately tuned delays also give rise to multiresonant
responses, yet the successive delays warranting an optimal coherence of
excitations obey different relations with regards to the inherent time scales
of neuronal dynamics. This leads to denser coherence resonance patterns in the
delay-strength parameter plane. The robustness of these findings to the
introduction of delay in the excitatory feedback, to noise, and to the number
of coupled neurons is determined. Mechanisms underlying our observations are
revealed, and it is suggested that the regularity of spiking across neuronal
networks can be optimized in an unexpectedly rich variety of ways, depending on
the type of coupling and the duration of delays.Comment: 7 two-column pages, 6 figures; accepted for publication in
Communications in Nonlinear Science and Numerical Simulatio
Spike Timing and Reliability in Cortical Pyramidal Neurons: Effects of EPSC Kinetics, Input Synchronization and Background Noise on Spike Timing
In vivo studies have shown that neurons in the neocortex can generate action potentials at high temporal precision. The mechanisms controlling timing and reliability of action potential generation in neocortical neurons, however, are still poorly understood. Here we investigated the temporal precision and reliability of spike firing in cortical layer V pyramidal cells at near-threshold membrane potentials. Timing and reliability of spike responses were a function of EPSC kinetics, temporal jitter of population excitatory inputs, and of background synaptic noise. We used somatic current injection to mimic population synaptic input events and measured spike probability and spike time precision (STP), the latter defined as the time window (Ξt) holding 80% of response spikes. EPSC rise and decay times were varied over the known physiological spectrum. At spike threshold level, EPSC decay time had a stronger influence on STP than rise time. Generally, STP was highest (β€2.45 ms) in response to synchronous compounds of EPSCs with fast rise and decay kinetics. Compounds with slow EPSC kinetics (decay time constants>6 ms) triggered spikes at lower temporal precision (β₯6.58 ms). We found an overall linear relationship between STP and spike delay. The difference in STP between fast and slow compound EPSCs could be reduced by incrementing the amplitude of slow compound EPSCs. The introduction of a temporal jitter to compound EPSCs had a comparatively small effect on STP, with a tenfold increase in jitter resulting in only a five fold decrease in STP. In the presence of simulated synaptic background activity, precisely timed spikes could still be induced by fast EPSCs, but not by slow EPSCs
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