Abstract

Simple SummaryA computational model of primates’ early visual processing, showing orientation selectivity, is presented. The system importantly integrates two key elements: (1) a neuromorphic spike-decoding structure that considerably resembles the circuitry between layers IV and II/III of the primary visual cortex, both in topology and operation; (2) the plasticity of intrinsic excitability, to embed recent findings about the operation of the same area. The model is proposed as a tool for the analysis and reproduction of the orientation selectivity phenomenon, whose underlying neuronal-level computational mechanisms are today the subject of intense scrutiny. In response to rotated Gabor patches the model is able to exhibit realistic orientation tuning curves and to reproduce responses similar to those found in neurophysiological recordings from the primary visual cortex obtained under the same task, considering different stages of the network. This demonstrates its aptness to capture the mechanisms underlying the evoked response in the primary visual cortex. Our tool is available online, and can be expanded to other experiments using a dedicated software library developed by the authors, to elucidate the computational mechanisms underlying orientation selectivity.Since the first half of the twentieth century, numerous studies have been conducted on how the visual cortex encodes basic image features. One of the hallmarks of basic feature extraction is the phenomenon of orientation selectivity, of which the underlying neuronal-level computational mechanisms remain partially unclear despite being intensively investigated. In this work we present a reduced visual system model (RVSM) of the first level of scene analysis, involving the retina, the lateral geniculate nucleus and the primary visual cortex (V1), showing orientation selectivity. The detection core of the RVSM is the neuromorphic spike-decoding structure MNSD, which is able to learn and recognize parallel spike sequences and considerably resembles the neuronal microcircuits of V1 in both topology and operation. This structure is equipped with plasticity of intrinsic excitability to embed recent findings about V1 operation. The RVSM, which embeds 81 groups of MNSD arranged in 4 oriented columns, is tested using sets of rotated Gabor patches as input. Finally, synthetic visual evoked activity generated by the RVSM is compared with real neurophysiological signal from V1 area: (1) postsynaptic activity of human subjects obtained by magnetoencephalography and (2) spiking activity of macaques obtained by multi-tetrode arrays. The system is implemented using the NEST simulator. The results attest to a good level of resemblance between the model response and real neurophysiological recordings. As the RVSM is available online, and the model parameters can be customized by the user, we propose it as a tool to elucidate the computational mechanisms underlying orientation selectivity.

Highlights

  • The crux of most of the unresolved questions of neuroscience lies in the mechanisms of neuronal cooperation and parallel processing of information in the brain [1]

  • We assess the ability of the reduced visual system model (RVSM) in reproducing (1) the orientation tuning curves of the pinwheel cortical columns, and (2) the shape of the electrophysiological signal when responding to orientated Gabor patches

  • Regarding the orientation tuning showed by the whole pinwheel, we presented to the model images with angles ranging from 0◦ to 180◦, and measured the activity produced by the four oriented columns of the pinwheel, obtaining a behavior that resembles that of the real case

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Summary

Introduction

The crux of most of the unresolved questions of neuroscience lies in the mechanisms of neuronal cooperation and parallel processing of information in the brain [1]. A broad palette of realistic neuronal models is available to today’s computational neuroscientists, there are very few neural circuits, if any, of which the working mechanisms are known with certainty. One of the emblems of this deadlock is represented by the open debate on whether neurons code information using firing rates or precise spike timings [2,3,4]. In this regard, combining theory of neural computation with experimental observations, a promiscuous frame emerges. While rate coding was previously considered a more plausible and robust strategy than temporal coding, in recent years more and more importance has been given to the significance of the temporal organization of spike patterns [5,6]

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