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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2021-04-01
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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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