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Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function

Adult rats equipped with a sensory prosthesis, which transduced infrared (IR) signals into electrical signals delivered to somatosensory cortex (S1), took approximately 4 d to learn a four-choice IR discrimination task. Here, we show that when such IR signals are projected to the primary visual cort...

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Autores principales: Thomson, Eric E., Zea, Ivan, Windham, William, Thenaisie, Yohann, Walker, Cameron, Pedowitz, Jason, França, Wendy, Graneiro, Ana L., Nicolelis, Miguel A.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739531/
https://www.ncbi.nlm.nih.gov/pubmed/29279860
http://dx.doi.org/10.1523/ENEURO.0262-17.2017
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author Thomson, Eric E.
Zea, Ivan
Windham, William
Thenaisie, Yohann
Walker, Cameron
Pedowitz, Jason
França, Wendy
Graneiro, Ana L.
Nicolelis, Miguel A.L.
author_facet Thomson, Eric E.
Zea, Ivan
Windham, William
Thenaisie, Yohann
Walker, Cameron
Pedowitz, Jason
França, Wendy
Graneiro, Ana L.
Nicolelis, Miguel A.L.
author_sort Thomson, Eric E.
collection PubMed
description Adult rats equipped with a sensory prosthesis, which transduced infrared (IR) signals into electrical signals delivered to somatosensory cortex (S1), took approximately 4 d to learn a four-choice IR discrimination task. Here, we show that when such IR signals are projected to the primary visual cortex (V1), rats that are pretrained in a visual-discrimination task typically learn the same IR discrimination task on their first day of training. However, without prior training on a visual discrimination task, the learning rates for S1- and V1-implanted animals converged, suggesting there is no intrinsic difference in learning rate between the two areas. We also discovered that animals were able to integrate IR information into the ongoing visual processing stream in V1, performing a visual-IR integration task in which they had to combine IR and visual information. Furthermore, when the IR prosthesis was implanted in S1, rats showed no impairment in their ability to use their whiskers to perform a tactile discrimination task. Instead, in some rats, this ability was actually enhanced. Cumulatively, these findings suggest that cortical sensory neuroprostheses can rapidly augment the representational scope of primary sensory areas, integrating novel sources of information into ongoing processing while incurring minimal loss of native function.
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spelling pubmed-57395312017-12-26 Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function Thomson, Eric E. Zea, Ivan Windham, William Thenaisie, Yohann Walker, Cameron Pedowitz, Jason França, Wendy Graneiro, Ana L. Nicolelis, Miguel A.L. eNeuro New Research Adult rats equipped with a sensory prosthesis, which transduced infrared (IR) signals into electrical signals delivered to somatosensory cortex (S1), took approximately 4 d to learn a four-choice IR discrimination task. Here, we show that when such IR signals are projected to the primary visual cortex (V1), rats that are pretrained in a visual-discrimination task typically learn the same IR discrimination task on their first day of training. However, without prior training on a visual discrimination task, the learning rates for S1- and V1-implanted animals converged, suggesting there is no intrinsic difference in learning rate between the two areas. We also discovered that animals were able to integrate IR information into the ongoing visual processing stream in V1, performing a visual-IR integration task in which they had to combine IR and visual information. Furthermore, when the IR prosthesis was implanted in S1, rats showed no impairment in their ability to use their whiskers to perform a tactile discrimination task. Instead, in some rats, this ability was actually enhanced. Cumulatively, these findings suggest that cortical sensory neuroprostheses can rapidly augment the representational scope of primary sensory areas, integrating novel sources of information into ongoing processing while incurring minimal loss of native function. Society for Neuroscience 2017-12-20 /pmc/articles/PMC5739531/ /pubmed/29279860 http://dx.doi.org/10.1523/ENEURO.0262-17.2017 Text en Copyright © 2017 Thomson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Thomson, Eric E.
Zea, Ivan
Windham, William
Thenaisie, Yohann
Walker, Cameron
Pedowitz, Jason
França, Wendy
Graneiro, Ana L.
Nicolelis, Miguel A.L.
Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function
title Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function
title_full Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function
title_fullStr Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function
title_full_unstemmed Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function
title_short Cortical Neuroprosthesis Merges Visible and Invisible Light Without Impairing Native Sensory Function
title_sort cortical neuroprosthesis merges visible and invisible light without impairing native sensory function
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739531/
https://www.ncbi.nlm.nih.gov/pubmed/29279860
http://dx.doi.org/10.1523/ENEURO.0262-17.2017
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