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Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes
The visual system is one of the most accessible routes to study the central nervous system under pathological conditions, such as in multiple sclerosis (MS). Non-invasive visual evoked potential (VEP) and optical coherence tomography (OCT) were used to assess visual function and neuroretinal thickne...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051229/ https://www.ncbi.nlm.nih.gov/pubmed/35495042 http://dx.doi.org/10.3389/fnins.2022.820155 |
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author | Marenna, Silvia Huang, Su-Chun Dalla Costa, Gloria d’Isa, Raffaele Castoldi, Valerio Rossi, Elena Comi, Giancarlo Leocani, Letizia |
author_facet | Marenna, Silvia Huang, Su-Chun Dalla Costa, Gloria d’Isa, Raffaele Castoldi, Valerio Rossi, Elena Comi, Giancarlo Leocani, Letizia |
author_sort | Marenna, Silvia |
collection | PubMed |
description | The visual system is one of the most accessible routes to study the central nervous system under pathological conditions, such as in multiple sclerosis (MS). Non-invasive visual evoked potential (VEP) and optical coherence tomography (OCT) were used to assess visual function and neuroretinal thickness in C57BL/6 taking 0.2% cuprizone for 7 weeks and at 5, 8, 12, and 15 days after returning to a normal diet. VEPs were significantly delayed starting from 4 weeks on cuprizone, with progressive recovery off cuprizone, becoming significant at day 8, complete at day 15. In contrast, OCT and neurofilament staining showed no significant axonal thinning. Optic nerve histology indicated that whilst there was significant myelin loss at 7 weeks on the cuprizone diet compared with healthy mice, at 15 days off cuprizone diet demyelination was significantly less severe. The number of Iba 1(+) cells was found increased in cuprizone mice at 7 weeks on and 15 days off cuprizone. The combined use of VEPs and OCT allowed us to characterize non-invasively, in vivo, the functional and structural changes associated with demyelination and remyelination in a preclinical model of MS. This approach contributes to the non-invasive study of possible effective treatments to promote remyelination in demyelinating pathologies. |
format | Online Article Text |
id | pubmed-9051229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90512292022-04-30 Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes Marenna, Silvia Huang, Su-Chun Dalla Costa, Gloria d’Isa, Raffaele Castoldi, Valerio Rossi, Elena Comi, Giancarlo Leocani, Letizia Front Neurosci Neuroscience The visual system is one of the most accessible routes to study the central nervous system under pathological conditions, such as in multiple sclerosis (MS). Non-invasive visual evoked potential (VEP) and optical coherence tomography (OCT) were used to assess visual function and neuroretinal thickness in C57BL/6 taking 0.2% cuprizone for 7 weeks and at 5, 8, 12, and 15 days after returning to a normal diet. VEPs were significantly delayed starting from 4 weeks on cuprizone, with progressive recovery off cuprizone, becoming significant at day 8, complete at day 15. In contrast, OCT and neurofilament staining showed no significant axonal thinning. Optic nerve histology indicated that whilst there was significant myelin loss at 7 weeks on the cuprizone diet compared with healthy mice, at 15 days off cuprizone diet demyelination was significantly less severe. The number of Iba 1(+) cells was found increased in cuprizone mice at 7 weeks on and 15 days off cuprizone. The combined use of VEPs and OCT allowed us to characterize non-invasively, in vivo, the functional and structural changes associated with demyelination and remyelination in a preclinical model of MS. This approach contributes to the non-invasive study of possible effective treatments to promote remyelination in demyelinating pathologies. Frontiers Media S.A. 2022-04-15 /pmc/articles/PMC9051229/ /pubmed/35495042 http://dx.doi.org/10.3389/fnins.2022.820155 Text en Copyright © 2022 Marenna, Huang, Dalla Costa, d’Isa, Castoldi, Rossi, Comi and Leocani. 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 | Neuroscience Marenna, Silvia Huang, Su-Chun Dalla Costa, Gloria d’Isa, Raffaele Castoldi, Valerio Rossi, Elena Comi, Giancarlo Leocani, Letizia Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes |
title | Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes |
title_full | Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes |
title_fullStr | Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes |
title_full_unstemmed | Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes |
title_short | Visual Evoked Potentials to Monitor Myelin Cuprizone-Induced Functional Changes |
title_sort | visual evoked potentials to monitor myelin cuprizone-induced functional changes |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051229/ https://www.ncbi.nlm.nih.gov/pubmed/35495042 http://dx.doi.org/10.3389/fnins.2022.820155 |
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