7,258 research outputs found
Decorrelation of neural-network activity by inhibitory feedback
Correlations in spike-train ensembles can seriously impair the encoding of
information by their spatio-temporal structure. An inevitable source of
correlation in finite neural networks is common presynaptic input to pairs of
neurons. Recent theoretical and experimental studies demonstrate that spike
correlations in recurrent neural networks are considerably smaller than
expected based on the amount of shared presynaptic input. By means of a linear
network model and simulations of networks of leaky integrate-and-fire neurons,
we show that shared-input correlations are efficiently suppressed by inhibitory
feedback. To elucidate the effect of feedback, we compare the responses of the
intact recurrent network and systems where the statistics of the feedback
channel is perturbed. The suppression of spike-train correlations and
population-rate fluctuations by inhibitory feedback can be observed both in
purely inhibitory and in excitatory-inhibitory networks. The effect is fully
understood by a linear theory and becomes already apparent at the macroscopic
level of the population averaged activity. At the microscopic level,
shared-input correlations are suppressed by spike-train correlations: In purely
inhibitory networks, they are canceled by negative spike-train correlations. In
excitatory-inhibitory networks, spike-train correlations are typically
positive. Here, the suppression of input correlations is not a result of the
mere existence of correlations between excitatory (E) and inhibitory (I)
neurons, but a consequence of a particular structure of correlations among the
three possible pairings (EE, EI, II)
Locking of correlated neural activity to ongoing oscillations
Population-wide oscillations are ubiquitously observed in mesoscopic signals
of cortical activity. In these network states a global oscillatory cycle
modulates the propensity of neurons to fire. Synchronous activation of neurons
has been hypothesized to be a separate channel of signal processing information
in the brain. A salient question is therefore if and how oscillations interact
with spike synchrony and in how far these channels can be considered separate.
Experiments indeed showed that correlated spiking co-modulates with the static
firing rate and is also tightly locked to the phase of beta-oscillations. While
the dependence of correlations on the mean rate is well understood in
feed-forward networks, it remains unclear why and by which mechanisms
correlations tightly lock to an oscillatory cycle. We here demonstrate that
such correlated activation of pairs of neurons is qualitatively explained by
periodically-driven random networks. We identify the mechanisms by which
covariances depend on a driving periodic stimulus. Mean-field theory combined
with linear response theory yields closed-form expressions for the
cyclostationary mean activities and pairwise zero-time-lag covariances of
binary recurrent random networks. Two distinct mechanisms cause time-dependent
covariances: the modulation of the susceptibility of single neurons (via the
external input and network feedback) and the time-varying variances of single
unit activities. For some parameters, the effectively inhibitory recurrent
feedback leads to resonant covariances even if mean activities show
non-resonant behavior. Our analytical results open the question of
time-modulated synchronous activity to a quantitative analysis.Comment: 57 pages, 12 figures, published versio
The Spatial Structure of Stimuli Shapes the Timescale of Correlations in Population Spiking Activity
Throughout the central nervous system, the timescale over which pairs of neural spike trains are correlated is shaped by stimulus structure and behavioral context. Such shaping is thought to underlie important changes in the neural code, but the neural circuitry responsible is largely unknown. In this study, we investigate a stimulus-induced shaping of pairwise spike train correlations in the electrosensory system of weakly electric fish. Simultaneous single unit recordings of principal electrosensory cells show that an increase in the spatial extent of stimuli increases correlations at short (~10 ms) timescales while simultaneously reducing correlations at long (~100 ms) timescales. A spiking network model of the first two stages of electrosensory processing replicates this correlation shaping, under the assumptions that spatially broad stimuli both saturate feedforward afferent input and recruit an open-loop inhibitory feedback pathway. Our model predictions are experimentally verified using both the natural heterogeneity of the electrosensory system and pharmacological blockade of descending feedback projections. For weak stimuli, linear response analysis of the spiking network shows that the reduction of long timescale correlation for spatially broad stimuli is similar to correlation cancellation mechanisms previously suggested to be operative in mammalian cortex. The mechanism for correlation shaping supports population-level filtering of irrelevant distractor stimuli, thereby enhancing the population response to relevant prey and conspecific communication inputs. © 2012 Litwin-Kumar et al
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
Learning as a phenomenon occurring in a critical state
Recent physiological measurements have provided clear evidence about
scale-free avalanche brain activity and EEG spectra, feeding the classical
enigma of how such a chaotic system can ever learn or respond in a controlled
and reproducible way. Models for learning, like neural networks or perceptrons,
have traditionally avoided strong fluctuations. Conversely, we propose that
brain activity having features typical of systems at a critical point,
represents a crucial ingredient for learning. We present here a study which
provides novel insights toward the understanding of the problem. Our model is
able to reproduce quantitatively the experimentally observed critical state of
the brain and, at the same time, learns and remembers logical rules including
the exclusive OR (XOR), which has posed difficulties to several previous
attempts. We implement the model on a network with topological properties close
to the functionality network in real brains. Learning occurs via plastic
adaptation of synaptic strengths and exhibits universal features. We find that
the learning performance and the average time required to learn are controlled
by the strength of plastic adaptation, in a way independent of the specific
task assigned to the system. Even complex rules can be learned provided that
the plastic adaptation is sufficiently slow.Comment: 5 pages, 5 figure
The effect of heterogeneity on decorrelation mechanisms in spiking neural networks: a neuromorphic-hardware study
High-level brain function such as memory, classification or reasoning can be
realized by means of recurrent networks of simplified model neurons. Analog
neuromorphic hardware constitutes a fast and energy efficient substrate for the
implementation of such neural computing architectures in technical applications
and neuroscientific research. The functional performance of neural networks is
often critically dependent on the level of correlations in the neural activity.
In finite networks, correlations are typically inevitable due to shared
presynaptic input. Recent theoretical studies have shown that inhibitory
feedback, abundant in biological neural networks, can actively suppress these
shared-input correlations and thereby enable neurons to fire nearly
independently. For networks of spiking neurons, the decorrelating effect of
inhibitory feedback has so far been explicitly demonstrated only for
homogeneous networks of neurons with linear sub-threshold dynamics. Theory,
however, suggests that the effect is a general phenomenon, present in any
system with sufficient inhibitory feedback, irrespective of the details of the
network structure or the neuronal and synaptic properties. Here, we investigate
the effect of network heterogeneity on correlations in sparse, random networks
of inhibitory neurons with non-linear, conductance-based synapses. Emulations
of these networks on the analog neuromorphic hardware system Spikey allow us to
test the efficiency of decorrelation by inhibitory feedback in the presence of
hardware-specific heterogeneities. The configurability of the hardware
substrate enables us to modulate the extent of heterogeneity in a systematic
manner. We selectively study the effects of shared input and recurrent
connections on correlations in membrane potentials and spike trains. Our
results confirm ...Comment: 20 pages, 10 figures, supplement
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
Neural mechanisms of social learning in the female mouse
Social interactions are often powerful drivers of learning. In female mice, mating creates a long-lasting sensory memory for the pheromones of the stud male that alters neuroendocrine responses to his chemosignals for many weeks. The cellular and synaptic correlates of pheromonal learning, however, remain unclear. We examined local circuit changes in the accessory olfactory bulb (AOB) using targeted ex vivo recordings of mating-activated neurons tagged with a fluorescent reporter. Imprinting led to striking plasticity in the intrinsic membrane excitability of projection neurons (mitral cells, MCs) that dramatically curtailed their responsiveness, suggesting a novel cellular substrate for pheromonal learning. Plasticity was selectively expressed in the MC ensembles activated by the stud male, consistent with formation of memories for specific individuals. Finally, MC excitability gained atypical activity-dependence whose slow dynamics strongly attenuated firing on timescales of several minutes. This unusual form of AOB plasticity may act to filter sustained or repetitive sensory signals.R21 DC013894 - NIDCD NIH HH
Intrinsically-generated fluctuating activity in excitatory-inhibitory networks
Recurrent networks of non-linear units display a variety of dynamical regimes
depending on the structure of their synaptic connectivity. A particularly
remarkable phenomenon is the appearance of strongly fluctuating, chaotic
activity in networks of deterministic, but randomly connected rate units. How
this type of intrinsi- cally generated fluctuations appears in more realistic
networks of spiking neurons has been a long standing question. To ease the
comparison between rate and spiking networks, recent works investigated the
dynami- cal regimes of randomly-connected rate networks with segregated
excitatory and inhibitory populations, and firing rates constrained to be
positive. These works derived general dynamical mean field (DMF) equations
describing the fluctuating dynamics, but solved these equations only in the
case of purely inhibitory networks. Using a simplified excitatory-inhibitory
architecture in which DMF equations are more easily tractable, here we show
that the presence of excitation qualitatively modifies the fluctuating activity
compared to purely inhibitory networks. In presence of excitation,
intrinsically generated fluctuations induce a strong increase in mean firing
rates, a phenomenon that is much weaker in purely inhibitory networks.
Excitation moreover induces two different fluctuating regimes: for moderate
overall coupling, recurrent inhibition is sufficient to stabilize fluctuations,
for strong coupling, firing rates are stabilized solely by the upper bound
imposed on activity, even if inhibition is stronger than excitation. These
results extend to more general network architectures, and to rate networks
receiving noisy inputs mimicking spiking activity. Finally, we show that
signatures of the second dynamical regime appear in networks of
integrate-and-fire neurons
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