Cargando…

Inflammatory demyelination alters subcortical visual circuits

BACKGROUND: Multiple sclerosis (MS) is an inflammatory demyelinating disease classically associated with axonal damage and loss; more recently, however, synaptic changes have been recognized as additional contributing factors. An anatomical area commonly affected in MS is the visual pathway; yet, ch...

Descripción completa

Detalles Bibliográficos
Autores principales: Araújo, Sheila Espírito Santo, Mendonça, Henrique Rocha, Wheeler, Natalie A., Campello-Costa, Paula, Jacobs, Kimberle M., Gomes, Flávia C. A., Fox, Michael A., Fuss, Babette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562979/
https://www.ncbi.nlm.nih.gov/pubmed/28821276
http://dx.doi.org/10.1186/s12974-017-0936-0
_version_ 1783258047975522304
author Araújo, Sheila Espírito Santo
Mendonça, Henrique Rocha
Wheeler, Natalie A.
Campello-Costa, Paula
Jacobs, Kimberle M.
Gomes, Flávia C. A.
Fox, Michael A.
Fuss, Babette
author_facet Araújo, Sheila Espírito Santo
Mendonça, Henrique Rocha
Wheeler, Natalie A.
Campello-Costa, Paula
Jacobs, Kimberle M.
Gomes, Flávia C. A.
Fox, Michael A.
Fuss, Babette
author_sort Araújo, Sheila Espírito Santo
collection PubMed
description BACKGROUND: Multiple sclerosis (MS) is an inflammatory demyelinating disease classically associated with axonal damage and loss; more recently, however, synaptic changes have been recognized as additional contributing factors. An anatomical area commonly affected in MS is the visual pathway; yet, changes other than those associated with inflammatory demyelination of the optic nerve, i.e., optic neuritis, have not been described in detail. METHODS: Adult mice were subjected to a diet containing cuprizone to mimic certain aspects of inflammatory demyelination as seen in MS. Demyelination and inflammation were assessed by real-time polymerase chain reaction and immunohistochemistry. Synaptic changes associated with inflammatory demyelination in the dorsal lateral geniculate nucleus (dLGN) were determined by immunohistochemistry, Western blot analysis, and electrophysiological field potential recordings. RESULTS: In the cuprizone model, demyelination was observed in retinorecipient regions of the subcortical visual system, in particular the dLGN, where it was found accompanied by microglia activation and astrogliosis. In contrast, anterior parts of the pathway, i.e., the optic nerve and tract, appeared largely unaffected. Under the inflammatory demyelinating conditions, as seen in the dLGN of cuprizone-treated mice, there was an overall decrease in excitatory synaptic inputs from retinal ganglion cells. At the same time, the number of synaptic complexes arising from gamma-aminobutyric acid (GABA)-generating inhibitory neurons was found increased, as were the synapses that contain the N-methyl-d-aspartate receptor (NMDAR) subunit GluN2B and converge onto inhibitory neurons. These synaptic changes were functionally found associated with a shift toward an overall increase in network inhibition. CONCLUSIONS: Using the cuprizone model of inflammatory demyelination, our data reveal a novel form of synaptic (mal)adaption in the CNS that is characterized by a shift of the excitation/inhibition balance toward inhibitory network activity associated with an increase in GABAergic inhibitory synapses and a possible increase in excitatory input onto inhibitory interneurons. In addition, our data recognize the cuprizone model as a suitable tool in which to assess the effects of inflammatory demyelination on subcortical retinorecipient regions of the visual system, such as the dLGN, in the absence of overt optic neuritis.
format Online
Article
Text
id pubmed-5562979
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-55629792017-08-21 Inflammatory demyelination alters subcortical visual circuits Araújo, Sheila Espírito Santo Mendonça, Henrique Rocha Wheeler, Natalie A. Campello-Costa, Paula Jacobs, Kimberle M. Gomes, Flávia C. A. Fox, Michael A. Fuss, Babette J Neuroinflammation Research BACKGROUND: Multiple sclerosis (MS) is an inflammatory demyelinating disease classically associated with axonal damage and loss; more recently, however, synaptic changes have been recognized as additional contributing factors. An anatomical area commonly affected in MS is the visual pathway; yet, changes other than those associated with inflammatory demyelination of the optic nerve, i.e., optic neuritis, have not been described in detail. METHODS: Adult mice were subjected to a diet containing cuprizone to mimic certain aspects of inflammatory demyelination as seen in MS. Demyelination and inflammation were assessed by real-time polymerase chain reaction and immunohistochemistry. Synaptic changes associated with inflammatory demyelination in the dorsal lateral geniculate nucleus (dLGN) were determined by immunohistochemistry, Western blot analysis, and electrophysiological field potential recordings. RESULTS: In the cuprizone model, demyelination was observed in retinorecipient regions of the subcortical visual system, in particular the dLGN, where it was found accompanied by microglia activation and astrogliosis. In contrast, anterior parts of the pathway, i.e., the optic nerve and tract, appeared largely unaffected. Under the inflammatory demyelinating conditions, as seen in the dLGN of cuprizone-treated mice, there was an overall decrease in excitatory synaptic inputs from retinal ganglion cells. At the same time, the number of synaptic complexes arising from gamma-aminobutyric acid (GABA)-generating inhibitory neurons was found increased, as were the synapses that contain the N-methyl-d-aspartate receptor (NMDAR) subunit GluN2B and converge onto inhibitory neurons. These synaptic changes were functionally found associated with a shift toward an overall increase in network inhibition. CONCLUSIONS: Using the cuprizone model of inflammatory demyelination, our data reveal a novel form of synaptic (mal)adaption in the CNS that is characterized by a shift of the excitation/inhibition balance toward inhibitory network activity associated with an increase in GABAergic inhibitory synapses and a possible increase in excitatory input onto inhibitory interneurons. In addition, our data recognize the cuprizone model as a suitable tool in which to assess the effects of inflammatory demyelination on subcortical retinorecipient regions of the visual system, such as the dLGN, in the absence of overt optic neuritis. BioMed Central 2017-08-18 /pmc/articles/PMC5562979/ /pubmed/28821276 http://dx.doi.org/10.1186/s12974-017-0936-0 Text en © The Author(s). 2017 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
Araújo, Sheila Espírito Santo
Mendonça, Henrique Rocha
Wheeler, Natalie A.
Campello-Costa, Paula
Jacobs, Kimberle M.
Gomes, Flávia C. A.
Fox, Michael A.
Fuss, Babette
Inflammatory demyelination alters subcortical visual circuits
title Inflammatory demyelination alters subcortical visual circuits
title_full Inflammatory demyelination alters subcortical visual circuits
title_fullStr Inflammatory demyelination alters subcortical visual circuits
title_full_unstemmed Inflammatory demyelination alters subcortical visual circuits
title_short Inflammatory demyelination alters subcortical visual circuits
title_sort inflammatory demyelination alters subcortical visual circuits
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562979/
https://www.ncbi.nlm.nih.gov/pubmed/28821276
http://dx.doi.org/10.1186/s12974-017-0936-0
work_keys_str_mv AT araujosheilaespiritosanto inflammatorydemyelinationalterssubcorticalvisualcircuits
AT mendoncahenriquerocha inflammatorydemyelinationalterssubcorticalvisualcircuits
AT wheelernataliea inflammatorydemyelinationalterssubcorticalvisualcircuits
AT campellocostapaula inflammatorydemyelinationalterssubcorticalvisualcircuits
AT jacobskimberlem inflammatorydemyelinationalterssubcorticalvisualcircuits
AT gomesflaviaca inflammatorydemyelinationalterssubcorticalvisualcircuits
AT foxmichaela inflammatorydemyelinationalterssubcorticalvisualcircuits
AT fussbabette inflammatorydemyelinationalterssubcorticalvisualcircuits