Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex

Abstract Although multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained...

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Main Authors: Paul VanGilder, Ying Shi, Gregory Apker, Christopher A. Buneo
Format: Article
Language:English
Published: Nature Publishing Group 2021-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-88278-5
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spelling doaj-b5f7136d3d314725946bc2660e8c0d3b2021-05-02T11:35:42ZengNature Publishing GroupScientific Reports2045-23222021-04-0111111410.1038/s41598-021-88278-5Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortexPaul VanGilder0Ying Shi1Gregory Apker2Christopher A. Buneo3School of Biological and Health Systems Engineering, Arizona State UniversitySchool of Biological and Health Systems Engineering, Arizona State UniversitySchool of Biological and Health Systems Engineering, Arizona State UniversitySchool of Biological and Health Systems Engineering, Arizona State UniversityAbstract Although multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained from the superior parietal lobule (SPL) as non-human primates performed a reaching task with either unimodal (proprioceptive) or bimodal (visual-proprioceptive) sensory feedback. Based on previous analyses of spiking activity, we hypothesized that evoked LFP responses would be tuned to arm location but would be suppressed on bimodal trials, relative to unimodal trials. We also expected to see a substantial number of recording sites with enhanced beta band spectral power for only one set of feedback conditions (e.g. unimodal or bimodal), as was previously observed for spiking activity. We found that evoked activity and beta band power were tuned to arm location at many individual sites, though this tuning often differed between unimodal and bimodal trials. Across the population, both evoked and beta activity were consistent with feedback-dependent tuning to arm location, while beta band activity also showed evidence of response suppression on bimodal trials. The results suggest that multisensory interactions can alter the tuning and gain of arm position-related LFP activity in the SPL.https://doi.org/10.1038/s41598-021-88278-5
collection DOAJ
language English
format Article
sources DOAJ
author Paul VanGilder
Ying Shi
Gregory Apker
Christopher A. Buneo
spellingShingle Paul VanGilder
Ying Shi
Gregory Apker
Christopher A. Buneo
Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
Scientific Reports
author_facet Paul VanGilder
Ying Shi
Gregory Apker
Christopher A. Buneo
author_sort Paul VanGilder
title Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_short Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_full Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_fullStr Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_full_unstemmed Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_sort sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-04-01
description Abstract Although multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained from the superior parietal lobule (SPL) as non-human primates performed a reaching task with either unimodal (proprioceptive) or bimodal (visual-proprioceptive) sensory feedback. Based on previous analyses of spiking activity, we hypothesized that evoked LFP responses would be tuned to arm location but would be suppressed on bimodal trials, relative to unimodal trials. We also expected to see a substantial number of recording sites with enhanced beta band spectral power for only one set of feedback conditions (e.g. unimodal or bimodal), as was previously observed for spiking activity. We found that evoked activity and beta band power were tuned to arm location at many individual sites, though this tuning often differed between unimodal and bimodal trials. Across the population, both evoked and beta activity were consistent with feedback-dependent tuning to arm location, while beta band activity also showed evidence of response suppression on bimodal trials. The results suggest that multisensory interactions can alter the tuning and gain of arm position-related LFP activity in the SPL.
url https://doi.org/10.1038/s41598-021-88278-5
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