6,078 research outputs found
Inhibitory synchrony as a mechanism for attentional gain modulation
Recordings from area V4 of monkeys have revealed that when the focus of
attention is on a visual stimulus within the receptive field of a cortical
neuron, two distinct changes can occur: The firing rate of the neuron can
change and there can be an increase in the coherence between spikes and the
local field potential in the gamma-frequency range (30-50 Hz). The hypothesis
explored here is that these observed effects of attention could be a
consequence of changes in the synchrony of local interneuron networks. We
performed computer simulations of a Hodgkin-Huxley type neuron driven by a
constant depolarizing current, I, representing visual stimulation and a
modulatory inhibitory input representing the effects of attention via local
interneuron networks. We observed that the neuron's firing rate and the
coherence of its output spike train with the synaptic inputs was modulated by
the degree of synchrony of the inhibitory inputs. The model suggest that the
observed changes in firing rate and coherence of neurons in the visual cortex
could be controlled by top-down inputs that regulated the coherence in the
activity of a local inhibitory network discharging at gamma frequencies.Comment: J.Physiology (Paris) in press, 11 figure
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
Mechanisms of Zero-Lag Synchronization in Cortical Motifs
Zero-lag synchronization between distant cortical areas has been observed in
a diversity of experimental data sets and between many different regions of the
brain. Several computational mechanisms have been proposed to account for such
isochronous synchronization in the presence of long conduction delays: Of
these, the phenomenon of "dynamical relaying" - a mechanism that relies on a
specific network motif - has proven to be the most robust with respect to
parameter mismatch and system noise. Surprisingly, despite a contrary belief in
the community, the common driving motif is an unreliable means of establishing
zero-lag synchrony. Although dynamical relaying has been validated in empirical
and computational studies, the deeper dynamical mechanisms and comparison to
dynamics on other motifs is lacking. By systematically comparing
synchronization on a variety of small motifs, we establish that the presence of
a single reciprocally connected pair - a "resonance pair" - plays a crucial
role in disambiguating those motifs that foster zero-lag synchrony in the
presence of conduction delays (such as dynamical relaying) from those that do
not (such as the common driving triad). Remarkably, minor structural changes to
the common driving motif that incorporate a reciprocal pair recover robust
zero-lag synchrony. The findings are observed in computational models of
spiking neurons, populations of spiking neurons and neural mass models, and
arise whether the oscillatory systems are periodic, chaotic, noise-free or
driven by stochastic inputs. The influence of the resonance pair is also robust
to parameter mismatch and asymmetrical time delays amongst the elements of the
motif. We call this manner of facilitating zero-lag synchrony resonance-induced
synchronization, outline the conditions for its occurrence, and propose that it
may be a general mechanism to promote zero-lag synchrony in the brain.Comment: 41 pages, 12 figures, and 11 supplementary figure
Neurosystems: brain rhythms and cognitive processing
Neuronal rhythms are ubiquitous features of brain dynamics, and are highly correlated with cognitive processing. However, the relationship between the physiological mechanisms producing these rhythms and the functions associated with the rhythms remains mysterious. This article investigates the contributions of rhythms to basic cognitive computations (such as filtering signals by coherence and/or frequency) and to major cognitive functions (such as attention and multi-modal coordination). We offer support to the premise that the physiology underlying brain rhythms plays an essential role in how these rhythms facilitate some cognitive operations.098352 - Wellcome Trust; 5R01NS067199 - NINDS NIH HH
Neural spike train synchronization indices: Definitions, interpretations, and applications
A comparison of previously defined spike train synchronization indices is undertaken within a stochastic point process framework. The second-order cumulant density (covariance density) is shown to be common to all the indices. Simulation studies were used to investigate the sampling variability of a single index based on the second-order cumulant. The simulations used a paired motoneurone model and a paired regular spiking cortical neurone model. The sampling variability of spike trains generated under identical conditions from the paired motoneurone model varied from 50% to 160% of the estimated value. On theoretical grounds, and on the basis of simulated data a rate dependence is present in all synchronization indices. The application of coherence and pooled coherence estimates to the issue of synchronization indices is considered. This alternative frequency domain approach allows an arbitrary number of spike train pairs to be evaluated for statistically significant differences, and combined into a single population measure. The pooled coherence framework allows pooled time domain measures to be derived, application of this to the simulated data is illustrated. Data from the cortical neurone model is generated over a wide range of firing rates (1-250 spikes/s). The pooled coherence framework correctly characterizes the sampling variability as not significant over this wide operating range. The broader applicability of this approach to multielectrode array data is briefly discussed
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
Neuronal synchrony: peculiarity and generality
Synchronization in neuronal systems is a new and intriguing application of dynamical systems theory. Why are neuronal systems different as a subject for synchronization? (1) Neurons in themselves are multidimensional nonlinear systems that are able to exhibit a wide variety of different activity patterns. Their “dynamical repertoire” includes regular or chaotic spiking, regular or chaotic bursting, multistability, and complex transient regimes. (2) Usually, neuronal oscillations are the result of the cooperative activity of many synaptically connected neurons (a neuronal circuit). Thus, it is necessary to consider synchronization between different neuronal circuits as well. (3) The synapses that implement the coupling between neurons are also dynamical elements and their intrinsic dynamics influences the process of synchronization or entrainment significantly. In this review we will focus on four new problems: (i) the synchronization in minimal neuronal networks with plastic synapses (synchronization with activity dependent coupling), (ii) synchronization of bursts that are generated by a group of nonsymmetrically coupled inhibitory neurons (heteroclinic synchronization), (iii) the coordination of activities of two coupled neuronal networks (partial synchronization of small composite structures), and (iv) coarse grained synchronization in larger systems (synchronization on a mesoscopic scale
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