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Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury
ABSTRACT: Cortical areas have the capacity of large‐scale reorganization following sensory deafferentation. However, it remains unclear whether this phenomenon is a unique process that homogeneously affects the entire deprived cortical region or whether it is susceptible to changes depending on neur...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292026/ https://www.ncbi.nlm.nih.gov/pubmed/34418097 http://dx.doi.org/10.1113/JP281901 |
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author | Zaforas, Marta Rosa, Juliana M. Alonso‐Calviño, Elena Fernández‐López, Elena Miguel‐Quesada, Claudia Oliviero, Antonio Aguilar, Juan |
author_facet | Zaforas, Marta Rosa, Juliana M. Alonso‐Calviño, Elena Fernández‐López, Elena Miguel‐Quesada, Claudia Oliviero, Antonio Aguilar, Juan |
author_sort | Zaforas, Marta |
collection | PubMed |
description | ABSTRACT: Cortical areas have the capacity of large‐scale reorganization following sensory deafferentation. However, it remains unclear whether this phenomenon is a unique process that homogeneously affects the entire deprived cortical region or whether it is susceptible to changes depending on neuronal networks across distinct cortical layers. Here, we studied how the local circuitry within each layer of the deafferented cortex forms the basis for neuroplastic changes after immediate thoracic spinal cord injury (SCI) in anaesthetized rats. In vivo electrophysiological recordings from deafferented hindlimb somatosensory cortex showed that SCI induces layer‐specific changes mediating evoked and spontaneous activity. In supragranular layer 2/3, SCI increased gamma oscillations and the ability of these neurons to initiate up‐states during spontaneous activity, suggesting an altered corticocortical network and/or intrinsic properties that may serve to maintain the excitability of the cortical column after deafferentation. On the other hand, SCI enhanced the infragranular layers’ ability to integrate evoked sensory inputs leading to increased and faster neuronal responses. Delayed evoked response onsets were also observed in layer 5/6, suggesting alterations in thalamocortical connectivity. Altogether, our data indicate that SCI immediately modifies the local circuitry within the deafferented cortex allowing supragranular layers to better integrate spontaneous corticocortical information, thus modifying column excitability, and infragranular layers to better integrate evoked sensory inputs to preserve subcortical outputs. These layer‐specific neuronal changes may guide the long‐term alterations in neuronal excitability and plasticity associated with the rearrangements of somatosensory networks and the appearance of central sensory pathologies usually associated with spinal cord injury. KEY POINTS: Sensory stimulation of forelimb produces cortical evoked responses in the somatosensory hindlimb cortex in a layer‐dependent manner. Spinal cord injury favours the input statistics of corticocortical connections between intact and deafferented cortices. After spinal cord injury supragranular layers exhibit better integration of spontaneous corticocortical information while infragranular layers exhibit better integration of evoked sensory stimulation. Cortical reorganization is a layer‐specific phenomenon. |
format | Online Article Text |
id | pubmed-9292026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92920262022-07-20 Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury Zaforas, Marta Rosa, Juliana M. Alonso‐Calviño, Elena Fernández‐López, Elena Miguel‐Quesada, Claudia Oliviero, Antonio Aguilar, Juan J Physiol Neuroscience ABSTRACT: Cortical areas have the capacity of large‐scale reorganization following sensory deafferentation. However, it remains unclear whether this phenomenon is a unique process that homogeneously affects the entire deprived cortical region or whether it is susceptible to changes depending on neuronal networks across distinct cortical layers. Here, we studied how the local circuitry within each layer of the deafferented cortex forms the basis for neuroplastic changes after immediate thoracic spinal cord injury (SCI) in anaesthetized rats. In vivo electrophysiological recordings from deafferented hindlimb somatosensory cortex showed that SCI induces layer‐specific changes mediating evoked and spontaneous activity. In supragranular layer 2/3, SCI increased gamma oscillations and the ability of these neurons to initiate up‐states during spontaneous activity, suggesting an altered corticocortical network and/or intrinsic properties that may serve to maintain the excitability of the cortical column after deafferentation. On the other hand, SCI enhanced the infragranular layers’ ability to integrate evoked sensory inputs leading to increased and faster neuronal responses. Delayed evoked response onsets were also observed in layer 5/6, suggesting alterations in thalamocortical connectivity. Altogether, our data indicate that SCI immediately modifies the local circuitry within the deafferented cortex allowing supragranular layers to better integrate spontaneous corticocortical information, thus modifying column excitability, and infragranular layers to better integrate evoked sensory inputs to preserve subcortical outputs. These layer‐specific neuronal changes may guide the long‐term alterations in neuronal excitability and plasticity associated with the rearrangements of somatosensory networks and the appearance of central sensory pathologies usually associated with spinal cord injury. KEY POINTS: Sensory stimulation of forelimb produces cortical evoked responses in the somatosensory hindlimb cortex in a layer‐dependent manner. Spinal cord injury favours the input statistics of corticocortical connections between intact and deafferented cortices. After spinal cord injury supragranular layers exhibit better integration of spontaneous corticocortical information while infragranular layers exhibit better integration of evoked sensory stimulation. Cortical reorganization is a layer‐specific phenomenon. John Wiley and Sons Inc. 2021-09-28 2021-10-15 /pmc/articles/PMC9292026/ /pubmed/34418097 http://dx.doi.org/10.1113/JP281901 Text en © 2021 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Neuroscience Zaforas, Marta Rosa, Juliana M. Alonso‐Calviño, Elena Fernández‐López, Elena Miguel‐Quesada, Claudia Oliviero, Antonio Aguilar, Juan Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
title | Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
title_full | Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
title_fullStr | Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
title_full_unstemmed | Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
title_short | Cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
title_sort | cortical layer‐specific modulation of neuronal activity after sensory deprivation due to spinal cord injury |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292026/ https://www.ncbi.nlm.nih.gov/pubmed/34418097 http://dx.doi.org/10.1113/JP281901 |
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