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      Identification of neural feature space from spike triggered covariance expressed as a function of PRC

      abstract
      1 , 2 , 3 , , 4 , 3 , 5 , 5 , 4 , 3 , 1
      BMC Neuroscience
      BioMed Central
      Nineteenth Annual Computational Neuroscience Meeting: CNS*2010
      24–30 July 2010

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          Abstract

          For the purpose of elucidating the neural coding process based on the neural excitability mechanism, some researchers have investigated the relationship between the neural dynamics and the spike triggered stimulus ensemble (STE), which indicates what stimuli are more likely or less likely to induce neural spikes. Ermentrout et al. have analytically derived the relational equation between the phase response curve (PRC) and the spike triggered average (STA), which is the average of the STE, when regular spikes with a period are disturbed by sufficiently small white noise, as (1). Here, is the time relative to a spike, is the noise intensity, and is PRC [1]. Furthermore, they showed that Eq. (1) holds true for real neurons. Their study has made meaningful progress in relating the neural dynamics to the neural coding for real neurons. However, the STA is the first cumulant of the STE. In order to approximately identify the distribution of STE as a Gaussian, we should determine its second cumulant, called spike triggered covariance (STC). We derive the relational equation between STC and PRC on the basis of the formulation introduced in [2] and analytically solve it by the expansion used in [3]. The result is (2) where represents the Heaviside function which takes 1/2 at . Moreover, we analyze the eigenfunctions of in order to extract the neural feature space, which is a low dimensional subspace of the full stimulus space characterizing the stimulus encoded by neurons. The eigenfunctions associated with the positive and negative eigenvalues of are called the excitatory and suppressive eigenfunction, respectively. In this case, the stimuli in the subspace spanned by excitatory eigenfunctions cause shorter interspike intervals (ISIs) than , while the stimuli in the subspace spanned by suppressive eigenfunctions cause longer ISIs. Figure 1 shows the STC of a rat hippocampal CA1 pyramidal neuron as calculated by Eq. (2), where the PRC could be estimated by our algorithm [4]. Note that it is difficult to measure the STC for real neurons directly, because the number of neural spikes required for a stable calculation of STC is nearly square of the number required for the STA. Figure 1 suggests that the neural feature space of this rat hippocampal CA1 pyramidal neuron can be described by the four eigenfunctions in Fig. 1b. Figure. 1 left: STC of the rat hippocampal CA1 pyramidal neuron. (a) Eigenvalue spectrum of for the same neuron as illustrated in the left panel. (b) Excitatory (red) and suppressive (blue) eigenfunctions corresponding to the eigenvalues in (a).

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          Single neuron computation: from dynamical system to feature detector.

          White noise methods are a powerful tool for characterizing the computation performed by neural systems. These methods allow one to identify the feature or features that a neural system extracts from a complex input and to determine how these features are combined to drive the system's spiking response. These methods have also been applied to characterize the input-output relations of single neurons driven by synaptic inputs, simulated by direct current injection. To interpret the results of white noise analysis of single neurons, we would like to understand how the obtained feature space of a single neuron maps onto the biophysical properties of the membrane, in particular, the dynamics of ion channels. Here, through analysis of a simple dynamical model neuron, we draw explicit connections between the output of a white noise analysis and the underlying dynamical system. We find that under certain assumptions, the form of the relevant features is well defined by the parameters of the dynamical system. Further, we show that under some conditions, the feature space is spanned by the spike-triggered average and its successive order time derivatives.
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            Relating neural dynamics to neural coding.

            We demonstrate that two key theoretical objects used widely in computational neuroscience, the phase-resetting curve (PRC) from dynamics and the spike triggered average (STA) from statistical analysis, are closely related when neurons fire in a nearly regular manner and the stimulus is sufficiently small. We prove that the STA due to injected noisy current is proportional to the derivative of the PRC. We compare these analytic results with numerical calculations for the Hodgkin-Huxley neuron and we apply the method to neurons in the olfactory bulb of mice. This observation allows us to relate the stimulus-response properties of a neuron to its dynamics, bridging the gap between dynamical and information theoretic approaches to understanding brain computations and facilitating the interpretation of changes in channels and other cellular properties as influencing the representation of stimuli.
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              Temporal precision of spike response to fluctuating input in pulse-coupled networks of oscillating neurons.

              A single neuron is known to generate almost identical spike trains when the same fluctuating input is repeatedly applied. Here, we study the reliability of spike firing in a pulse-coupled network of oscillator neurons receiving fluctuating inputs. We can study the precise responses of the network as synchronization between uncoupled copies of the network by a common noisy input. To study the noise-induced synchronization between networks, we derive a self-consistent equation for the distribution of spike-time differences between the networks. Solving this equation, we elucidate how the spike precision changes as a function of the coupling strength.
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                Author and article information

                Conference
                BMC Neurosci
                BMC Neuroscience
                BioMed Central
                1471-2202
                2010
                20 July 2010
                : 11
                : Suppl 1
                : P14
                Affiliations
                [1 ]Dep. of Computational Intelligence and System Science, Tokyo Tech., Yokohama, 2268502, Japan
                [2 ]Research Fellow of the Japan Society for the Promotion of Science, JSPS, Tokyo, 1028471, Japan
                [3 ]Brain Science Institute, RIKEN, Wako, 3510198, Japan
                [4 ]Dep. of Complexity Science and Engineering, Univ. of Tokyo, Kashiwa, 2778561, Japan
                [5 ]Dep. of Life Science, Tokyo Univ. of Pharmacy and Life Science, Hachioji, 1920392, Japan
                Article
                1471-2202-11-S1-P14
                10.1186/1471-2202-11-S1-P14
                3090843
                6fb600a3-3afe-4ccd-a337-450363dd8bee
                Copyright ©2010 Ota et al; licensee BioMed Central Ltd.
                Nineteenth Annual Computational Neuroscience Meeting: CNS*2010
                San Antonio, TX, USA
                24–30 July 2010
                History
                Categories
                Poster Presentation

                Neurosciences
                Neurosciences

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