159 research outputs found

    Cortical topography of intracortical inhibition influences the speed of decision making

    Get PDF
    The neocortex contains orderly topographic maps; however, their functional role remains controversial. Theoretical studies have suggested a role in minimizing computational costs, whereas empirical studies have focused on spatial localization. Using a tactile multiple-choice reaction time (RT) task before and after the induction of perceptual learning through repetitive sensory stimulation, we extend the framework of cortical topographies by demonstrating that the topographic arrangement of intracortical inhibition contributes to the speed of human perceptual decision-making processes. RTs differ among fingers, displaying an inverted U-shaped function. Simulations using neural fields show the inverted U-shaped RT distribution as an emergent consequence of lateral inhibition. Weakening inhibition through learning shortens RTs, which is modeled through topographically reorganized inhibition. Whereas changes in decision making are often regarded as an outcome of higher cortical areas, our data show that the spatial layout of interaction processes within representational maps contributes to selection and decision-making processes

    Establishing, versus Maintaining, Brain Function: A Neuro-computational Model of Cortical Reorganization after Injury to the Immature Brain

    Full text link
    The effect of age at injury on outcome after acquired brain injury (ABI) has been the subject of much debate. Many argue that young brains are relatively tolerant of injury. A contrasting viewpoint due to Hebb argues that greater system integrity may be required for the initial establishment of a function than for preservation of an already-established function. A neuro-computational model of cortical map formation was adapted to examine effects of focal and distributed injury at various stages of development. This neural network model requires a period of training during which it self-organizes to establish cortical maps. Injuries were simulated by lesioning the model at various stages of this process and network function was monitored as "development" progressed to completion. Lesion effects are greater for larger, earlier, and distributed (multifocal) lesions. The mature system is relatively robust, particularly to focal injury. Activities in recovering systems injured at an early stage show changes that emerge after an asymptomatic interval. Early injuries cause qualitative changes in system behavior that emerge after a delay during which the effects of the injury are latent. Functions that are incompletely established at the time of injury may be vulnerable particularly to multifocal injury

    Insights into activity-dependent map formation from the retinotectal system: a middle-of-the-brain perspective

    Get PDF
    ABSTRACT: The development of orderly topographic maps in the central nervous system (CNS) results from a collaboration of chemoaffinity cues that establish the coarse organization of the projection and activity-dependent mechanisms that fine-tune the map. Using the retinotectal projection as a model system, we describe evidence that biochemical tags and patterned neural activity work in parallel to produce topographically ordered axonal projections. Finally, we review recent experiments in other CNS projections that support the proposition that cooperation between molecular guidance cues and activity-dependent processes constitutes a general paradigm for CNS map formation

    Hebbian Learning of the Statistical and Geometrical Structure of Visual Input

    Get PDF

    A Neural Network Model for the Development of Simple and Complex Cell Receptive Fields Within Cortical Maps of Orientation and Ocular Dominance

    Full text link
    Prenatal development of the primary visual cortex leads to simple cells with spatially distinct and oriented ON and OFF subregions. These simple cells are organized into spatial maps of orientation and ocular dominance that exhibit singularities, fractures, and linear zones. On a finer spatial scale, simple cells occur that are sensitive to similar orientations but opposite contrast polarities, and exhibit both even-symmetric and odd-symmetric receptive fields. Pooling of outputs from oppositely polarized simple cells leads to complex cells that respond to both contrast polarities. A neural network model is described which simulates how simple and complex cells self-organize starting from unsegregated and unoriented geniculocortical inputs during prenatal development. Neighboring simple cells that are sensitive to opposite contrast polarities develop from a combination of spatially short-range inhibition and high-gain recurrent habituative excitation between cells that obey membrane equations. Habituation, or depression, of synapses controls reset of cell activations both through enhanced ON responses and OFF antagonistic rebounds. Orientation and ocular dominance maps form when high-gain medium-range recurrent excitation and long-range inhibition interact with the short-range mechanisms. The resulting structure clarifies how simple and complex cells contribute to perceptual processes such as texture segregation and perceptual grouping.Air Force Office of Scientific Research (F49620-92-J-0334); British Petroleum (BP 89A-1204); National Science Foundation (IRI-90-24877); Office of Naval Research (N00014-91-J-4100); Defense Advanced Research Projects Agency and the Office of Naval Research (N00014-95-1-0409

    One-Shot Multi-Winner Self-Organizing Maps

    Get PDF
    There exist two different approaches to self-organizing maps (SOMs). One approach, rooted in theoretical neuroscience, uses SOMs as computational models of biological cortex. The other approach, taken in computer science and engineering, views SOMs as tools suitable to perform, for example, data visualization and pattern classification tasks. While the first approach emphasizes fidelity to neurobiological data, the latter stresses computational efficiency and effectiveness. In the research reported here, I developed and studied a class of SOMs that incorporates the multiple, simultaneous winner nodes implicit in many biologically-oriented SOMs, but determines the winners using the same efficient one-shot algorithm employed by computationally-oriented, single-winner SOMs. This was achieved by generalizing single-winner SOMs, using localized competitions. The resulting one-shot multi-winner SOM was found to support the formation of multiple adjacent, mirror-symmetric topographic maps. It constitutes the first computational model of mirror-image map formation, and raises questions about the role of Hebbian-type synaptic changes in the formation of mirror-symmetric maps that are often observed in the sensory neocortex of many species, including humans. The model unexpectedly predicted the occasional occurrence of adjacent, rotationally symmetric maps. It is natural to speculate that such atypically oriented maps might contribute to abnormal cortical information processing in some neurodevelopmental disorders. Traditional SOMs lack applicability to problems where the inputs are not single patterns, but temporal sequences of patterns. Several SOM extensions have been proposed as a remedy, but there is no standard for processing temporal sequences with SOMs. I focused on the task of learning unique spatial representations for non-trivial sets of temporal sequences. The one-shot multi-winner SOM extended by temporally-asymmetric Hebbian synapses proved effective when applied to this task. The learned representations retained information about sequence similarity. The feature maps that formed show that temporal sequence processing and map formation are not mutually exclusive. Since the sequence processing one-shot multi-winner SOM was trained with phonetic transcriptions of spoken words, the results can be related to the internalization of spoken words during language acquisition. A final redesign of the network and the subsequent multi-objective optimization of its parameters using a genetic algorithm produced a more effective system

    A Model of Motion Processing in the Visual Cortex Using Neural Field With Asymmetric Hebbian Learning

    Get PDF
    Neurons in the dorsal pathway of the visual cortex are thought to be involved in motion processing. The first site of motion processing is the primary visual cortex (V1), encoding the direction of motion in local receptive fields, with higher order motion processing happening in the middle temporal area (MT). Complex motion properties like optic flow are processed in higher cortical areas of the Medial Superior Temporal area (MST). In this study, a hierarchical neural field network model of motion processing is presented. The model architecture has an input layer followed by either one or cascade of two neural fields (NF): the first of these, NF1, represents V1, while the second, NF2, represents MT. A special feature of the model is that lateral connections used in the neural fields are trained by asymmetric Hebbian learning, imparting to the neural field the ability to process sequential information in motion stimuli. The model was trained using various traditional moving patterns such as bars, squares, gratings, plaids, and random dot stimulus. In the case of bar stimuli, the model had only a single NF, the neurons of which developed a direction map of the moving bar stimuli. Training a network with two NFs on moving square and moving plaids stimuli, we show that, while the neurons in NF1 respond to the direction of the component (such as gratings and edges) motion, the neurons in NF2 (analogous to MT) responding to the direction of the pattern (plaids, square object) motion. In the third study, a network with 2 NFs was simulated using random dot stimuli (RDS) with translational motion, and show that the NF2 neurons can encode the direction of the concurrent dot motion (also called translational flow motion), independent of the dot configuration. This translational RDS flow motion is decoded by a simple perceptron network (a layer above NF2) with an accuracy of 100% on train set and 90% on the test set, thereby demonstrating that the proposed network can generalize to new dot configurations. Also, the response properties of the model on different input stimuli closely resembled many of the known features of the neurons found in electrophysiological studies

    A Theory of the Transition to Critical Period Plasticity: Inhibition Selectively Suppresses Spontaneous Activity

    Get PDF
    SummaryWhat causes critical periods (CPs) to open? For the best-studied case, ocular dominance plasticity in primary visual cortex in response to monocular deprivation (MD), the maturation of inhibition is necessary and sufficient. How does inhibition open the CP? We present a theory: the transition from pre-CP to CP plasticity arises because inhibition preferentially suppresses responses to spontaneous relative to visually driven input activity, switching learning cues from internal to external sources. This differs from previous proposals in (1) arguing that the CP can open without changes in plasticity mechanisms when activity patterns become more sensitive to sensory experience through circuit development, and (2) explaining not simply a transition from no plasticity to plasticity, but a change in outcome of MD-induced plasticity from pre-CP to CP. More broadly, hierarchical organization of sensory-motor pathways may develop through a cascade of CPs induced as circuit maturation progresses from “lower” to “higher” cortical areas
    • 

    corecore