Visual Population Receptive Fields in People with Schizophrenia Have Reduced Inhibitory Surrounds.

Elaine J Anderson, Marc S Tibber, D Sam Schwarzkopf, Sukhwinder S Shergill, Emilio Fernandez-Egea, Geraint Rees, Steven C Dakin

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience 2017;37(6):1546-1556

PMID: 28025253

Abstract

People with schizophrenia (SZ) experience abnormal visual perception on a range of visual tasks, which have been linked to abnormal synaptic transmission and an imbalance between cortical excitation and inhibition. However, differences in the underlying architecture of visual cortex neurons, which might explain these visual anomalies, have yet to be reported Here, we probed the neural basis of these deficits using fMRI and population receptive field (pRF) mapping to infer properties of visually responsive neurons in people with SZ. We employed a difference-of-Gaussian model to capture the center-surround configuration of the pRF, providing critical information about the spatial scale of the pRFs inhibitory surround. Our analysis reveals that SZ is associated with reduced pRF size in early retinotopic visual cortex, as well as a reduction in size and depth of the inhibitory surround in V1, V2, and V4. We consider how reduced inhibition might explain the diverse range of visual deficits reported in SZ. People with schizophrenia (SZ) experience abnormal perception on a range of visual tasks, which has been linked to abnormal synaptic transmission and an imbalance between cortical excitation/inhibition. However, associated differences in the functional architecture of visual cortex neurons have yet to be reported We used fMRI and population receptive field (pRF) mapping to demonstrate that the fine-grained functional architecture of visual cortex in people with SZ differs from unaffected controls. SZ is associated with reduced pRF size in early retinotopic visual cortex largely due to reduced inhibitory surrounds. An imbalance between cortical excitation and inhibition could drive such a change in the center-surround pRF configuration and ultimately explain the range of visual deficits experienced in SZ.

Copyright © 2017 Anderson et al.

Address: Institute of Ophthalmology, [email protected].; Institute of Cognitive Neuroscience.; Wellcome Trust Centre for Neuroimaging, and.; Institute of Ophthalmology.; Experimental Psychology, University College London, London, United Kingdom.; Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.; South London and Maudsley National Health Service Foundation Trust, London, United Kingdom.; Clozapine Clinic, Cambridgeshire and Peterborough National Health Service Foundation Trust, and.; Department of Psychiatry, Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom, and.; School of Optometry and Vision Science, University of Auckland, Auckland, New Zealand.
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