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      Human Parietal Cortex Structure Predicts Individual Differences in Perceptual Rivalry

      brief-report
      1 , , 1 , 2 , 3 , 1 , 2
      Current Biology
      Cell Press
      SYSNEURO

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          Summary

          When visual input has conflicting interpretations, conscious perception can alternate spontaneously between competing interpretations [ 1]. There is a large amount of unexplained variability between individuals in the rate of such spontaneous alternations in perception [ 2–5]. We hypothesized that variability in perceptual rivalry might be reflected in individual differences in brain structure, because brain structure can exhibit systematic relationships with an individual's cognitive experiences and skills [ 6–9]. To test this notion, we examined in a large group of individuals how cortical thickness, local gray-matter density, and local white-matter integrity correlate with individuals' alternation rate for a bistable, rotating structure-from-motion stimulus [ 10]. All of these macroscopic measures of brain structure consistently revealed that the structure of bilateral superior parietal lobes (SPL) could account for interindividual variability in perceptual alternation rate. Furthermore, we examined whether the bilateral SPL regions play a causal role in the rate of perceptual alternations by using transcranial magnetic stimulation (TMS) and found that transient disruption of these areas indeed decreases the rate of perceptual alternations. These findings demonstrate a direct relationship between structure of SPL and individuals' perceptual switch rate.

          Abstract

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          Highlights

          ► Structure of superior parietal lobe (SPL) predicts switch rate in perceptual rivalry ► White-matter integrity in SPL correlates with individuals' switch rate ► Deactivation of SPL with transcranial magnetic stimulation slows perceptual rivalry

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          Most cited references26

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          Structural covariance in the human cortex.

          The morphology of the human cortex varies remarkably across individuals, regardless of overall brain size. It is currently unclear whether related cortical regions covary in gray matter density, as a result of mutually trophic influences or common experience-related plasticity. We acquired a structural magnetic resonance imaging scan from 172 subjects and extracted the regional gray matter densities from 12 readily identifiable regions of interest involved in sensorimotor or higher-order cognitive functions. We then used these values to predict regional densities in the remaining areas of the cortex, using voxel-based morphometry. This revealed patterns of positive and negative covariance that provide insight into the topographical organization of multiple cortical regions. We report that the gray matter density of a region is a good predictor of the density of the homotopic region in the contralateral hemisphere, with the striking exception of primary visual cortex. Whereas some regions express patterns of regional covariance that are mirror symmetrical relative to the interhemispheric fissure, other regions express asymmetric patterns of regional covariance. Finally, patterns of covariance are remarkably consistent between males and females, with the exception of the left amygdala, which is positively associated with the left and right anterior inferior temporal cortex in males and with the right angular gyrus in females. Our study establishes that the density of different cortical regions is coordinated within an individual. The coordinated variations we report are likely to be determined by both genetic and environmental factors and may be the basis for differences in individual behavior.
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            Neural correlates of perceptual rivalry in the human brain.

            When dissimilar images are presented to the two eyes, perception alternates spontaneously between each monocular view, a phenomenon called binocular rivalry. Functional brain imaging in humans was used to study the neural basis of these subjective perceptual changes. Cortical regions whose activity reflected perceptual transitions included extrastriate areas of the ventral visual pathway, and parietal and frontal regions that have been implicated in spatial attention; whereas the extrastriate areas were also engaged by nonrivalrous perceptual changes, activity in the frontoparietal cortex was specifically associated with perceptual alternation only during rivalry. These results suggest that frontoparietal areas play a central role in conscious perception, biasing the content of visual awareness toward abstract internal representations of visual scenes, rather than simply toward space.
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              Transient neural activity in human parietal cortex during spatial attention shifts.

              Observers viewing a complex visual scene selectively attend to relevant locations or objects and ignore irrelevant ones. Selective attention to an object enhances its neural representation in extrastriate cortex, compared with those of unattended objects, via top-down attentional control signals. The posterior parietal cortex is centrally involved in this control of spatial attention. We examined brain activity during attention shifts using rapid, event-related fMRI of human observers as they covertly shifted attention between two peripheral spatial locations. Activation in extrastriate cortex increased after a shift of attention to the contralateral visual field and remained high during sustained contralateral attention. The time course of activity was substantially different in posterior parietal cortex, where transient increases in activation accompanied shifts of attention in either direction. This result suggests that activation of the parietal cortex is associated with a discrete signal to shift spatial attention, and is not the source of a signal to continuously maintain the current attentive state.
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                Author and article information

                Journal
                Curr Biol
                Curr. Biol
                Current Biology
                Cell Press
                0960-9822
                1879-0445
                28 September 2010
                28 September 2010
                : 20
                : 18-4
                : 1626-1630
                Affiliations
                [1 ]UCL Institute of Cognitive Neuroscience, University College London, 17 Queen Square, London WC1N 3AR, UK
                [2 ]Wellcome Trust Centre for Neuroimaging, University College London, 12 Queen Square, London WC1N 3BG, UK
                [3 ]Interacting Minds Project, Institute of Anthropology, Archaeology and Linguistics, Aarhus University and Centre of Functionally Integrative Neuroscience, Aarhus University Hospital, Norrebrogade 44, Building 10G, 8000 Aarhus C, Denmark
                Author notes
                []Corresponding author r.kanai@ 123456ucl.ac.uk
                Article
                CURBIO8275
                10.1016/j.cub.2010.07.027
                2949566
                20727757
                9cd71305-09ab-4bdd-b4f6-7e9b7732c190
                © 2010 ELL & Excerpta Medica.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 21 May 2010
                : 28 June 2010
                : 13 July 2010
                Categories
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                Life sciences
                sysneuro
                Life sciences
                sysneuro

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