58 research outputs found

    25th annual computational neuroscience meeting: CNS-2016

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    The same neuron may play different functional roles in the neural circuits to which it belongs. For example, neurons in the Tritonia pedal ganglia may participate in variable phases of the swim motor rhythms [1]. While such neuronal functional variability is likely to play a major role the delivery of the functionality of neural systems, it is difficult to study it in most nervous systems. We work on the pyloric rhythm network of the crustacean stomatogastric ganglion (STG) [2]. Typically network models of the STG treat neurons of the same functional type as a single model neuron (e.g. PD neurons), assuming the same conductance parameters for these neurons and implying their synchronous firing [3, 4]. However, simultaneous recording of PD neurons shows differences between the timings of spikes of these neurons. This may indicate functional variability of these neurons. Here we modelled separately the two PD neurons of the STG in a multi-neuron model of the pyloric network. Our neuron models comply with known correlations between conductance parameters of ionic currents. Our results reproduce the experimental finding of increasing spike time distance between spikes originating from the two model PD neurons during their synchronised burst phase. The PD neuron with the larger calcium conductance generates its spikes before the other PD neuron. Larger potassium conductance values in the follower neuron imply longer delays between spikes, see Fig. 17.Neuromodulators change the conductance parameters of neurons and maintain the ratios of these parameters [5]. Our results show that such changes may shift the individual contribution of two PD neurons to the PD-phase of the pyloric rhythm altering their functionality within this rhythm. Our work paves the way towards an accessible experimental and computational framework for the analysis of the mechanisms and impact of functional variability of neurons within the neural circuits to which they belong

    Within-quadrant position and orientation specificity after extensive orientation discrimination learning is related to performance gains during late learning

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    The last decade has seen the emergence of new views about the mechanisms underlying specificity (or, conversely, generalization) of visual skill learning. Here, we trained participants at orientation discrimination paradigm at a peripheral position to induce position and orientation specificity and to test its underlying mechanisms. Specifically, we aimed to test whether the within-quadrant spatial gradient of generalization is determined by cortical magnification, which would show that retinotopic plasticity contributes to learning and specificity. Additionally, we aimed to test whether late parts of the learning relate differently to specificity compared to early parts. This is relevant in the context of double training papers, which suggest that rule-based mechanisms of specificity in fast, early learning also would apply to late, slower learning. Our data showed partial but significant position and orientation specificity within quadrants. Interestingly, specificity was greatest for those participants who had continued to show threshold decreases during the last five sessions of training (late, asymptotic learning). Performance gains during early learning were less related to specificity. A trend for skill to spread over larger distances towards periphery than towards central vision suggested contributions to transfer of early visual areas showing cortical magnification of central vision. Control experiments however did not support this hypothesis. In summary, our study demonstrates significant specificity after extensive perceptual learning, and indicates that asymptotic learning recruits specific mechanisms that promote specificity, and that may not be recruited yet in early parts of the learning. The contributions of different mechanisms to early and late learning suggests that following these different learning periods, generalization relies on different principles and is subjected to different limits

    Quantifying Neural Oscillatory Synchronization: A Comparison between Spectral Coherence and Phase-Locking Value Approaches

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    Synchronization or phase-locking between oscillating neuronal groups is considered to be important for coordination of information among cortical networks. Spectral coherence is a commonly used approach to quantify phase locking between neural signals. We systematically explored the validity of spectral coherence measures for quantifying synchronization among neural oscillators. To that aim, we simulated coupled oscillatory signals that exhibited synchronization dynamics using an abstract phase-oscillator model as well as interacting gamma-generating spiking neural networks. We found that, within a large parameter range, the spectral coherence measure deviated substantially from the expected phase-locking. Moreover, spectral coherence did not converge to the expected value with increasing signal-to-noise ratio. We found that spectral coherence particularly failed when oscillators were in the partially (intermittent) synchronized state, which we expect to be the most likely state for neural synchronization. The failure was due to the fast frequency and amplitude changes induced by synchronization forces. We then investigated whether spectral coherence reflected the information flow among networks measured by transfer entropy (TE) of spike trains. We found that spectral coherence failed to robustly reflect changes in synchrony-mediated information flow between neural networks in many instances. As an alternative approach we explored a phase-locking value (PLV) method based on the reconstruction of the instantaneous phase. As one approach for reconstructing instantaneous phase, we used the Hilbert Transform (HT) preceded by Singular Spectrum Decomposition (SSD) of the signal. PLV estimates have broad applicability as they do not rely on stationarity, and, unlike spectral coherence, they enable more accurate estimations of oscillatory synchronization across a wide range of different synchronization regimes, and better tracking of synchronization-mediated information flow among networks

    Data from: A quantitative theory of gamma synchronization in macaque V1

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    Gamma-band synchronization coordinates brief periods of excitability in oscillating neuronal populations to optimize information transmission during sensation and cognition. Commonly, a stable, shared frequency over time is considered a condition for functional neural synchronization. Here, we demonstrate the opposite: instantaneous frequency modulations are critical to regulate phase relations and synchronization. In monkey visual area V1, nearby local populations driven by different visual stimulation showed different gamma frequencies. When similar enough, these frequencies continually attracted and repulsed each other, which enabled preferred phase relations to be maintained in periods of minimized frequency difference. Crucially, the precise dynamics of frequencies and phases across a wide range of stimulus conditions was predicted from a physics theory that describes how weakly coupled oscillators influence each other’s phase relations. Hence, the fundamental mathematical principle of synchronization through instantaneous frequency modulations applies to gamma in V1, and is likely generalizable to other brain regions and rhythms

    M1_session_1

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    Contains current-source density (CSD) signals from 3X 16-contact laminar probes inserted in macaque cortical area V1. Horizontal and vertical eye positions are added. Each trial consists of 1 sec baseline (gray screen while monkey is looking on fixation point) and 2sec stimulation period (square-wave grating with spatially varying contrast; monkey remains fixating). Information about the receptive field positions as well as seen local stimulus contrast for each probe is added to the data structure

    ring_PING_HH_data

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    Simulation of a ring-shaped PING network with spatial-defined connectivity and input drive to E-cells Fig3 = the network used for figure 3 in the main manuscript highEE= high interconnecitons strength between E-cells highII = high interconnection strength between I-cells noII = no interconnection strength between I-cells noEE= no interconnecitons strength between E-cells noiselevel1 = low noise level in the input AMPA train to E-cell noiselevel2 = higher noise level in the input AMPA train to E-cel
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