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Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons
Investigations of the mechanisms of touch perception and decoding has been hampered by difficulties in achieving invariant patterns of skin sensor activation. To obtain reproducible spatiotemporal patterns of activation of sensory afferents, we used an artificial fingertip equipped with an array of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379202/ https://www.ncbi.nlm.nih.gov/pubmed/28374841 http://dx.doi.org/10.1038/srep45898 |
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author | Oddo, Calogero M. Mazzoni, Alberto Spanne, Anton Enander, Jonas M. D. Mogensen, Hannes Bengtsson, Fredrik Camboni, Domenico Micera, Silvestro Jörntell, Henrik |
author_facet | Oddo, Calogero M. Mazzoni, Alberto Spanne, Anton Enander, Jonas M. D. Mogensen, Hannes Bengtsson, Fredrik Camboni, Domenico Micera, Silvestro Jörntell, Henrik |
author_sort | Oddo, Calogero M. |
collection | PubMed |
description | Investigations of the mechanisms of touch perception and decoding has been hampered by difficulties in achieving invariant patterns of skin sensor activation. To obtain reproducible spatiotemporal patterns of activation of sensory afferents, we used an artificial fingertip equipped with an array of neuromorphic sensors. The artificial fingertip was used to transduce real-world haptic stimuli into spatiotemporal patterns of spikes. These spike patterns were delivered to the skin afferents of the second digit of rats via an array of stimulation electrodes. Combined with low-noise intra- and extracellular recordings from neocortical neurons in vivo, this approach provided a previously inaccessible high resolution analysis of the representation of tactile information in the neocortical neuronal circuitry. The results indicate high information content in individual neurons and reveal multiple novel neuronal tactile coding features such as heterogeneous and complementary spatiotemporal input selectivity also between neighboring neurons. Such neuronal heterogeneity and complementariness can potentially support a very high decoding capacity in a limited population of neurons. Our results also indicate a potential neuroprosthetic approach to communicate with the brain at a very high resolution and provide a potential novel solution for evaluating the degree or state of neurological disease in animal models. |
format | Online Article Text |
id | pubmed-5379202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53792022017-04-10 Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons Oddo, Calogero M. Mazzoni, Alberto Spanne, Anton Enander, Jonas M. D. Mogensen, Hannes Bengtsson, Fredrik Camboni, Domenico Micera, Silvestro Jörntell, Henrik Sci Rep Article Investigations of the mechanisms of touch perception and decoding has been hampered by difficulties in achieving invariant patterns of skin sensor activation. To obtain reproducible spatiotemporal patterns of activation of sensory afferents, we used an artificial fingertip equipped with an array of neuromorphic sensors. The artificial fingertip was used to transduce real-world haptic stimuli into spatiotemporal patterns of spikes. These spike patterns were delivered to the skin afferents of the second digit of rats via an array of stimulation electrodes. Combined with low-noise intra- and extracellular recordings from neocortical neurons in vivo, this approach provided a previously inaccessible high resolution analysis of the representation of tactile information in the neocortical neuronal circuitry. The results indicate high information content in individual neurons and reveal multiple novel neuronal tactile coding features such as heterogeneous and complementary spatiotemporal input selectivity also between neighboring neurons. Such neuronal heterogeneity and complementariness can potentially support a very high decoding capacity in a limited population of neurons. Our results also indicate a potential neuroprosthetic approach to communicate with the brain at a very high resolution and provide a potential novel solution for evaluating the degree or state of neurological disease in animal models. Nature Publishing Group 2017-04-04 /pmc/articles/PMC5379202/ /pubmed/28374841 http://dx.doi.org/10.1038/srep45898 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Oddo, Calogero M. Mazzoni, Alberto Spanne, Anton Enander, Jonas M. D. Mogensen, Hannes Bengtsson, Fredrik Camboni, Domenico Micera, Silvestro Jörntell, Henrik Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
title | Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
title_full | Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
title_fullStr | Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
title_full_unstemmed | Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
title_short | Artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
title_sort | artificial spatiotemporal touch inputs reveal complementary decoding in neocortical neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379202/ https://www.ncbi.nlm.nih.gov/pubmed/28374841 http://dx.doi.org/10.1038/srep45898 |
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