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Thalamocortical-auditory network alterations following cuprizone‐induced demyelination

BACKGROUND: Demyelination and remyelination are common pathological processes in many neurological disorders, including multiple sclerosis (MS). Clinical evidence suggests extensive involvement of the thalamocortical (TC) system in patients suffering from MS. METHODS: Using murine brain slices of th...

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Autores principales: Ghaffarian, Nikoo, Mesgari, Masoud, Cerina, Manuela, Göbel, Kerstin, Budde, Thomas, Speckmann, Erwin-Josef, Meuth, Sven G., Gorji, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918138/
https://www.ncbi.nlm.nih.gov/pubmed/27334140
http://dx.doi.org/10.1186/s12974-016-0629-0
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author Ghaffarian, Nikoo
Mesgari, Masoud
Cerina, Manuela
Göbel, Kerstin
Budde, Thomas
Speckmann, Erwin-Josef
Meuth, Sven G.
Gorji, Ali
author_facet Ghaffarian, Nikoo
Mesgari, Masoud
Cerina, Manuela
Göbel, Kerstin
Budde, Thomas
Speckmann, Erwin-Josef
Meuth, Sven G.
Gorji, Ali
author_sort Ghaffarian, Nikoo
collection PubMed
description BACKGROUND: Demyelination and remyelination are common pathological processes in many neurological disorders, including multiple sclerosis (MS). Clinical evidence suggests extensive involvement of the thalamocortical (TC) system in patients suffering from MS. METHODS: Using murine brain slices of the primary auditory cortex, we investigated the functional consequences of cuprizone-induced de- and remyelination on neuronal activity and auditory TC synaptic transmission in vitro. RESULTS: Our results revealed an impact of myelin loss and restoration on intrinsic cellular firing patterns, synaptic transmission, and neuronal plasticity in layer 3 and 4 neurons of the auditory TC network. While there was a complex hyper- and depolarizing shift of the resting membrane potential, spontaneous and induced action potential firing was reduced during demyelination and early remyelination. In addition, excitatory postsynaptic potential amplitudes were decreased and induction of LTP was reduced during demyelination. CONCLUSIONS: These data indicate that demyelination-induced impairment of neurons and network activity within the TC system may underlie clinical symptoms observed in demyelinating diseases, corroborating human findings that disease progression is significantly correlated with microstructural tissue damage of the TC system. Further investigation into focal inflammation-induced demyelination models ex vivo and in vivo are needed to understand the functional implication of local and remote lesion formation on TC network activity in MS.
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spelling pubmed-49181382016-06-24 Thalamocortical-auditory network alterations following cuprizone‐induced demyelination Ghaffarian, Nikoo Mesgari, Masoud Cerina, Manuela Göbel, Kerstin Budde, Thomas Speckmann, Erwin-Josef Meuth, Sven G. Gorji, Ali J Neuroinflammation Research BACKGROUND: Demyelination and remyelination are common pathological processes in many neurological disorders, including multiple sclerosis (MS). Clinical evidence suggests extensive involvement of the thalamocortical (TC) system in patients suffering from MS. METHODS: Using murine brain slices of the primary auditory cortex, we investigated the functional consequences of cuprizone-induced de- and remyelination on neuronal activity and auditory TC synaptic transmission in vitro. RESULTS: Our results revealed an impact of myelin loss and restoration on intrinsic cellular firing patterns, synaptic transmission, and neuronal plasticity in layer 3 and 4 neurons of the auditory TC network. While there was a complex hyper- and depolarizing shift of the resting membrane potential, spontaneous and induced action potential firing was reduced during demyelination and early remyelination. In addition, excitatory postsynaptic potential amplitudes were decreased and induction of LTP was reduced during demyelination. CONCLUSIONS: These data indicate that demyelination-induced impairment of neurons and network activity within the TC system may underlie clinical symptoms observed in demyelinating diseases, corroborating human findings that disease progression is significantly correlated with microstructural tissue damage of the TC system. Further investigation into focal inflammation-induced demyelination models ex vivo and in vivo are needed to understand the functional implication of local and remote lesion formation on TC network activity in MS. BioMed Central 2016-06-22 /pmc/articles/PMC4918138/ /pubmed/27334140 http://dx.doi.org/10.1186/s12974-016-0629-0 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ghaffarian, Nikoo
Mesgari, Masoud
Cerina, Manuela
Göbel, Kerstin
Budde, Thomas
Speckmann, Erwin-Josef
Meuth, Sven G.
Gorji, Ali
Thalamocortical-auditory network alterations following cuprizone‐induced demyelination
title Thalamocortical-auditory network alterations following cuprizone‐induced demyelination
title_full Thalamocortical-auditory network alterations following cuprizone‐induced demyelination
title_fullStr Thalamocortical-auditory network alterations following cuprizone‐induced demyelination
title_full_unstemmed Thalamocortical-auditory network alterations following cuprizone‐induced demyelination
title_short Thalamocortical-auditory network alterations following cuprizone‐induced demyelination
title_sort thalamocortical-auditory network alterations following cuprizone‐induced demyelination
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918138/
https://www.ncbi.nlm.nih.gov/pubmed/27334140
http://dx.doi.org/10.1186/s12974-016-0629-0
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