Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Castejon, Carlos, Martin-Cortecero, Jesus, Nuñez, Angel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
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
_version_ 1784595419749154816
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
work_keys_str_mv AT castejoncarlos higherorderthalamicencodingofsomatosensorypatternsandbilateralevents
AT martincortecerojesus higherorderthalamicencodingofsomatosensorypatternsandbilateralevents
AT nunezangel higherorderthalamicencodingofsomatosensorypatternsandbilateralevents