Literature DB >> 26108951

Failure to use corollary discharge to remap visual target locations is associated with psychotic symptom severity in schizophrenia.

Lara Rösler1, Martin Rolfs2, Stefan van der Stigchel3, Sebastiaan F W Neggers4, Wiepke Cahn4, René S Kahn4, Katharine N Thakkar5.   

Abstract

Corollary discharge (CD) refers to "copies" of motor signals sent to sensory areas, allowing prediction of future sensory states. They enable the putative mechanisms supporting the distinction between self-generated and externally generated sensations. Accordingly, many authors have suggested that disturbed CD engenders psychotic symptoms of schizophrenia, which are characterized by agency distortions. CD also supports perceived visual stability across saccadic eye movements and is used to predict the postsaccadic retinal coordinates of visual stimuli, a process called remapping. We tested whether schizophrenia patients (SZP) show remapping disturbances as evidenced by systematic transsaccadic mislocalizations of visual targets. SZP and healthy controls (HC) performed a task in which a saccadic target disappeared upon saccade initiation and, after a brief delay, reappeared at a horizontally displaced position. HC judged the direction of this displacement accurately, despite spatial errors in saccade landing site, indicating that their comparison of the actual to predicted postsaccadic target location relied on accurate CD. SZP performed worse and relied more on saccade landing site as a proxy for the presaccadic target, consistent with disturbed CD. This remapping failure was strongest in patients with more severe psychotic symptoms, consistent with the theoretical link between disturbed CD and phenomenological experiences in schizophrenia.
Copyright © 2015 the American Physiological Society.

Entities:  

Keywords:  corollary discharge; efference copy; remapping; saccadic eye movements; schizophrenia

Mesh:

Substances:

Year:  2015        PMID: 26108951      PMCID: PMC4541139          DOI: 10.1152/jn.00155.2015

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


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