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Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events
The function of the higher-order sensory thalamus remains unclear. Here, the posterior medial (POm) nucleus of the thalamus was examined by in vivo extracellular recordings in anesthetized rats across a variety of contralateral, ipsilateral, and bilateral whisker sensory patterns. We found that POm...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573422/ https://www.ncbi.nlm.nih.gov/pubmed/34759802 http://dx.doi.org/10.3389/fncir.2021.752804 |
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author | Castejon, Carlos Martin-Cortecero, Jesus Nuñez, Angel |
author_facet | Castejon, Carlos Martin-Cortecero, Jesus Nuñez, Angel |
author_sort | Castejon, Carlos |
collection | PubMed |
description | The function of the higher-order sensory thalamus remains unclear. Here, the posterior medial (POm) nucleus of the thalamus was examined by in vivo extracellular recordings in anesthetized rats across a variety of contralateral, ipsilateral, and bilateral whisker sensory patterns. We found that POm was highly sensitive to multiwhisker stimuli involving diverse spatiotemporal interactions. Accurate increases in POm activity were produced during the overlapping time between spatial signals reflecting changes in the spatiotemporal structure of sensory patterns. In addition, our results showed for first time that POm was also able to respond to tactile stimulation of ipsilateral whiskers. This finding challenges the notion that the somatosensory thalamus only computes unilateral stimuli. We found that POm also integrates signals from both whisker pads and described how this integration is generated. Our results showed that ipsilateral activity reached one POm indirectly from the other POm and demonstrated a transmission of sensory activity between both nuclei through a functional POm-POm loop formed by thalamocortical, interhemispheric, and corticothalamic projections. The implication of different cortical areas was investigated revealing that S1 plays a central role in this POm-POm loop. Accordingly, the subcortical and cortical inputs allow POm but not the ventral posteromedial thalamic nucleus (VPM) to have sensory information from both sides of the body. This finding is in agreement with the higher-order nature of POm and can be considered to functionally differentiate and classify these thalamic nuclei. A possible functional role of these higher-order thalamic patterns of integrated activity in brain function is discussed. |
format | Online Article Text |
id | pubmed-8573422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85734222021-11-09 Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events Castejon, Carlos Martin-Cortecero, Jesus Nuñez, Angel Front Neural Circuits Neural Circuits The function of the higher-order sensory thalamus remains unclear. Here, the posterior medial (POm) nucleus of the thalamus was examined by in vivo extracellular recordings in anesthetized rats across a variety of contralateral, ipsilateral, and bilateral whisker sensory patterns. We found that POm was highly sensitive to multiwhisker stimuli involving diverse spatiotemporal interactions. Accurate increases in POm activity were produced during the overlapping time between spatial signals reflecting changes in the spatiotemporal structure of sensory patterns. In addition, our results showed for first time that POm was also able to respond to tactile stimulation of ipsilateral whiskers. This finding challenges the notion that the somatosensory thalamus only computes unilateral stimuli. We found that POm also integrates signals from both whisker pads and described how this integration is generated. Our results showed that ipsilateral activity reached one POm indirectly from the other POm and demonstrated a transmission of sensory activity between both nuclei through a functional POm-POm loop formed by thalamocortical, interhemispheric, and corticothalamic projections. The implication of different cortical areas was investigated revealing that S1 plays a central role in this POm-POm loop. Accordingly, the subcortical and cortical inputs allow POm but not the ventral posteromedial thalamic nucleus (VPM) to have sensory information from both sides of the body. This finding is in agreement with the higher-order nature of POm and can be considered to functionally differentiate and classify these thalamic nuclei. A possible functional role of these higher-order thalamic patterns of integrated activity in brain function is discussed. Frontiers Media S.A. 2021-10-25 /pmc/articles/PMC8573422/ /pubmed/34759802 http://dx.doi.org/10.3389/fncir.2021.752804 Text en Copyright © 2021 Castejon, Martin-Cortecero and Nuñez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neural Circuits Castejon, Carlos Martin-Cortecero, Jesus Nuñez, Angel Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events |
title | Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events |
title_full | Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events |
title_fullStr | Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events |
title_full_unstemmed | Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events |
title_short | Higher-Order Thalamic Encoding of Somatosensory Patterns and Bilateral Events |
title_sort | higher-order thalamic encoding of somatosensory patterns and bilateral events |
topic | Neural Circuits |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573422/ https://www.ncbi.nlm.nih.gov/pubmed/34759802 http://dx.doi.org/10.3389/fncir.2021.752804 |
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