Cargando…

Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice

Repetitive transcranial stimulation (rTMS) is an increasingly popular method to non-invasively modulate cortical excitability in research and clinical settings. During rTMS, low-intensity magnetic fields reach areas perifocal to the target brain region, however, effects of these low-intensity (LI-)...

Descripción completa

Detalles Bibliográficos
Autores principales: Makowiecki, Kalina, Garrett, Andrew, Harvey, Alan R., Rodger, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895738/
https://www.ncbi.nlm.nih.gov/pubmed/29643395
http://dx.doi.org/10.1038/s41598-018-23979-y
_version_ 1783313710097367040
author Makowiecki, Kalina
Garrett, Andrew
Harvey, Alan R.
Rodger, Jennifer
author_facet Makowiecki, Kalina
Garrett, Andrew
Harvey, Alan R.
Rodger, Jennifer
author_sort Makowiecki, Kalina
collection PubMed
description Repetitive transcranial stimulation (rTMS) is an increasingly popular method to non-invasively modulate cortical excitability in research and clinical settings. During rTMS, low-intensity magnetic fields reach areas perifocal to the target brain region, however, effects of these low-intensity (LI-) fields and how they interact with ongoing neural activity remains poorly defined. We evaluated whether coordinated neural activity during electromagnetic stimulation alters LI-rTMS effects on cortical excitability by comparing visually evoked potentials (VEP) and densities of parvalbumin-expressing (PV+) GABAergic interneurons in adult mouse visual cortex after LI-rTMS under different conditions: LI-rTMS applied during visually evoked (strong, coordinated) activity or in darkness (weak, spontaneous activity).We also compared response to LI-rTMS in wildtype and ephrin-A2A5(−/−) mice, which have visuotopic anomalies thought to disrupt coherence of visually-evoked cortical activity. Demonstrating that LI-rTMS effects in V1 require concurrent sensory-evoked activity, LI-rTMS delivered during visually-evoked activity increased PV+ immunoreactivity in both genotypes; however, VEP peak amplitudes changed only in wildtypes, consistent with intracortical disinhibition. We show, for the first time, that neural activity and the degree of coordination in cortical population activity interact with LI-rTMS to alter excitability in a context-dependent manner.
format Online
Article
Text
id pubmed-5895738
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-58957382018-04-20 Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice Makowiecki, Kalina Garrett, Andrew Harvey, Alan R. Rodger, Jennifer Sci Rep Article Repetitive transcranial stimulation (rTMS) is an increasingly popular method to non-invasively modulate cortical excitability in research and clinical settings. During rTMS, low-intensity magnetic fields reach areas perifocal to the target brain region, however, effects of these low-intensity (LI-) fields and how they interact with ongoing neural activity remains poorly defined. We evaluated whether coordinated neural activity during electromagnetic stimulation alters LI-rTMS effects on cortical excitability by comparing visually evoked potentials (VEP) and densities of parvalbumin-expressing (PV+) GABAergic interneurons in adult mouse visual cortex after LI-rTMS under different conditions: LI-rTMS applied during visually evoked (strong, coordinated) activity or in darkness (weak, spontaneous activity).We also compared response to LI-rTMS in wildtype and ephrin-A2A5(−/−) mice, which have visuotopic anomalies thought to disrupt coherence of visually-evoked cortical activity. Demonstrating that LI-rTMS effects in V1 require concurrent sensory-evoked activity, LI-rTMS delivered during visually-evoked activity increased PV+ immunoreactivity in both genotypes; however, VEP peak amplitudes changed only in wildtypes, consistent with intracortical disinhibition. We show, for the first time, that neural activity and the degree of coordination in cortical population activity interact with LI-rTMS to alter excitability in a context-dependent manner. Nature Publishing Group UK 2018-04-11 /pmc/articles/PMC5895738/ /pubmed/29643395 http://dx.doi.org/10.1038/s41598-018-23979-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Makowiecki, Kalina
Garrett, Andrew
Harvey, Alan R.
Rodger, Jennifer
Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
title Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
title_full Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
title_fullStr Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
title_full_unstemmed Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
title_short Low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
title_sort low-intensity repetitive transcranial magnetic stimulation requires concurrent visual system activity to modulate visual evoked potentials in adult mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895738/
https://www.ncbi.nlm.nih.gov/pubmed/29643395
http://dx.doi.org/10.1038/s41598-018-23979-y
work_keys_str_mv AT makowieckikalina lowintensityrepetitivetranscranialmagneticstimulationrequiresconcurrentvisualsystemactivitytomodulatevisualevokedpotentialsinadultmice
AT garrettandrew lowintensityrepetitivetranscranialmagneticstimulationrequiresconcurrentvisualsystemactivitytomodulatevisualevokedpotentialsinadultmice
AT harveyalanr lowintensityrepetitivetranscranialmagneticstimulationrequiresconcurrentvisualsystemactivitytomodulatevisualevokedpotentialsinadultmice
AT rodgerjennifer lowintensityrepetitivetranscranialmagneticstimulationrequiresconcurrentvisualsystemactivitytomodulatevisualevokedpotentialsinadultmice