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Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity

Bilateral eye enucleation at birth (BE) leads to an expansion of the primary somatosensory cortex (S1) in rat pups. Although increased growth of the somatosensory thalamo-cortical afferents (STCAs) in part explains S1 expansion, timing mechanisms governing S1 formation are also involved. In this wor...

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Autores principales: Martínez-Méndez, Raquel, Pérez-Torres, Daniel, Gómez-Chavarín, Margarita, Padilla-Cortés, Patricia, Fiordelisio, Tatiana, Gutiérrez-Ospina, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881598/
https://www.ncbi.nlm.nih.gov/pubmed/31799470
http://dx.doi.org/10.1016/j.ibror.2019.11.003
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author Martínez-Méndez, Raquel
Pérez-Torres, Daniel
Gómez-Chavarín, Margarita
Padilla-Cortés, Patricia
Fiordelisio, Tatiana
Gutiérrez-Ospina, Gabriel
author_facet Martínez-Méndez, Raquel
Pérez-Torres, Daniel
Gómez-Chavarín, Margarita
Padilla-Cortés, Patricia
Fiordelisio, Tatiana
Gutiérrez-Ospina, Gabriel
author_sort Martínez-Méndez, Raquel
collection PubMed
description Bilateral eye enucleation at birth (BE) leads to an expansion of the primary somatosensory cortex (S1) in rat pups. Although increased growth of the somatosensory thalamo-cortical afferents (STCAs) in part explains S1 expansion, timing mechanisms governing S1 formation are also involved. In this work, we begin the search of a developmental clock by intending to document the existence of putative clock neurons in the somatosensory thalamus (VPM) and S1 based upon changes of spontaneous spike amplitude; a biophysical property sensitive to circadian regulation; the latter known to be shifted by enucleation. In addition, we also evaluated whether STCAs growth rate and segregation timing were modified, as parameters the clock might time. We found that spontaneous spike amplitude transiently, but significantly, increased or decreased in VPM and S1 neurons of BE rat pups, respectively, as compared to their control counterparts. The growth rate and segregation timing of STCAs was, however, unaffected by BE. These results support the existence of a developmental clock that ticks differently in the VPM and S1 after BE. This observation, together with the fact that STCAs growth rate and segregation timing is unchanged, suggests that S1 expansion in BE rats may in part be controlled at the cortical level.
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spelling pubmed-68815982019-12-03 Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity Martínez-Méndez, Raquel Pérez-Torres, Daniel Gómez-Chavarín, Margarita Padilla-Cortés, Patricia Fiordelisio, Tatiana Gutiérrez-Ospina, Gabriel IBRO Rep Article Bilateral eye enucleation at birth (BE) leads to an expansion of the primary somatosensory cortex (S1) in rat pups. Although increased growth of the somatosensory thalamo-cortical afferents (STCAs) in part explains S1 expansion, timing mechanisms governing S1 formation are also involved. In this work, we begin the search of a developmental clock by intending to document the existence of putative clock neurons in the somatosensory thalamus (VPM) and S1 based upon changes of spontaneous spike amplitude; a biophysical property sensitive to circadian regulation; the latter known to be shifted by enucleation. In addition, we also evaluated whether STCAs growth rate and segregation timing were modified, as parameters the clock might time. We found that spontaneous spike amplitude transiently, but significantly, increased or decreased in VPM and S1 neurons of BE rat pups, respectively, as compared to their control counterparts. The growth rate and segregation timing of STCAs was, however, unaffected by BE. These results support the existence of a developmental clock that ticks differently in the VPM and S1 after BE. This observation, together with the fact that STCAs growth rate and segregation timing is unchanged, suggests that S1 expansion in BE rats may in part be controlled at the cortical level. Elsevier 2019-11-10 /pmc/articles/PMC6881598/ /pubmed/31799470 http://dx.doi.org/10.1016/j.ibror.2019.11.003 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Martínez-Méndez, Raquel
Pérez-Torres, Daniel
Gómez-Chavarín, Margarita
Padilla-Cortés, Patricia
Fiordelisio, Tatiana
Gutiérrez-Ospina, Gabriel
Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity
title Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity
title_full Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity
title_fullStr Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity
title_full_unstemmed Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity
title_short Bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: Implications for developmental cross-modal plasticity
title_sort bilateral enucleation at birth modifies calcium spike amplitude, but not frequency, in neurons of the somatosensory thalamus and cortex: implications for developmental cross-modal plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881598/
https://www.ncbi.nlm.nih.gov/pubmed/31799470
http://dx.doi.org/10.1016/j.ibror.2019.11.003
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