Cargando…

Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex

Transcranial direct current stimulation (tDCS) is increasingly used as a form of noninvasive brain stimulation to treat psychiatric disorders; however, its mechanism of action remains unclear. Prolonged visual stimulation (PVS) can enhance evoked EEG potentials (visually evoked potentials, VEPs) and...

Descripción completa

Detalles Bibliográficos
Autores principales: Frase, Lukas, Mertens, Lydia, Krahl, Arno, Bhatia, Kriti, Feige, Bernd, Heinrich, Sven P., Vestring, Stefan, Nissen, Christoph, Domschke, Katharina, Bach, Michael, Normann, Claus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791098/
https://www.ncbi.nlm.nih.gov/pubmed/33414402
http://dx.doi.org/10.1038/s41398-020-01134-4
_version_ 1783633537363083264
author Frase, Lukas
Mertens, Lydia
Krahl, Arno
Bhatia, Kriti
Feige, Bernd
Heinrich, Sven P.
Vestring, Stefan
Nissen, Christoph
Domschke, Katharina
Bach, Michael
Normann, Claus
author_facet Frase, Lukas
Mertens, Lydia
Krahl, Arno
Bhatia, Kriti
Feige, Bernd
Heinrich, Sven P.
Vestring, Stefan
Nissen, Christoph
Domschke, Katharina
Bach, Michael
Normann, Claus
author_sort Frase, Lukas
collection PubMed
description Transcranial direct current stimulation (tDCS) is increasingly used as a form of noninvasive brain stimulation to treat psychiatric disorders; however, its mechanism of action remains unclear. Prolonged visual stimulation (PVS) can enhance evoked EEG potentials (visually evoked potentials, VEPs) and has been proposed as a tool to examine long-term potentiation (LTP) in humans. The objective of the current study was to induce and analyze VEP plasticity and examine whether tDCS could either modulate or mimic plasticity changes induced by PVS. Thirty-eight healthy participants received tDCS, PVS, either treatment combined or neither treatment, with stimulation sessions being separated by one week. One session consisted of a baseline VEP measurement, one stimulation block, and six test VEP measurements. For PVS, a checkerboard reversal pattern was presented, and for tDCS, a constant current of 1 mA was applied via each bioccipital anodal target electrode for 10 min (Fig. S1). Both stimulation types decreased amplitudes of C1 compared to no stimulation (F = 10.1; p = 0.002) and led to a significantly smaller increase (PVS) or even decrease (tDCS) in N1 compared to no stimulation (F = 4.7; p = 0.034). While all stimulation types increased P1 amplitudes, the linear mixed effects model did not detect a significant difference between active stimulation and no stimulation. Combined stimulation induced sustained plastic modulation of C1 and N1 but with a smaller effect size than what would be expected for an additive effect. The results demonstrate that tDCS can directly induce LTP-like plasticity in the human cortex and suggest a mechanism of action of tDCS relying on the restoration of dysregulated synaptic plasticity in psychiatric disorders such as depression and schizophrenia.
format Online
Article
Text
id pubmed-7791098
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-77910982021-01-15 Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex Frase, Lukas Mertens, Lydia Krahl, Arno Bhatia, Kriti Feige, Bernd Heinrich, Sven P. Vestring, Stefan Nissen, Christoph Domschke, Katharina Bach, Michael Normann, Claus Transl Psychiatry Article Transcranial direct current stimulation (tDCS) is increasingly used as a form of noninvasive brain stimulation to treat psychiatric disorders; however, its mechanism of action remains unclear. Prolonged visual stimulation (PVS) can enhance evoked EEG potentials (visually evoked potentials, VEPs) and has been proposed as a tool to examine long-term potentiation (LTP) in humans. The objective of the current study was to induce and analyze VEP plasticity and examine whether tDCS could either modulate or mimic plasticity changes induced by PVS. Thirty-eight healthy participants received tDCS, PVS, either treatment combined or neither treatment, with stimulation sessions being separated by one week. One session consisted of a baseline VEP measurement, one stimulation block, and six test VEP measurements. For PVS, a checkerboard reversal pattern was presented, and for tDCS, a constant current of 1 mA was applied via each bioccipital anodal target electrode for 10 min (Fig. S1). Both stimulation types decreased amplitudes of C1 compared to no stimulation (F = 10.1; p = 0.002) and led to a significantly smaller increase (PVS) or even decrease (tDCS) in N1 compared to no stimulation (F = 4.7; p = 0.034). While all stimulation types increased P1 amplitudes, the linear mixed effects model did not detect a significant difference between active stimulation and no stimulation. Combined stimulation induced sustained plastic modulation of C1 and N1 but with a smaller effect size than what would be expected for an additive effect. The results demonstrate that tDCS can directly induce LTP-like plasticity in the human cortex and suggest a mechanism of action of tDCS relying on the restoration of dysregulated synaptic plasticity in psychiatric disorders such as depression and schizophrenia. Nature Publishing Group UK 2021-01-04 /pmc/articles/PMC7791098/ /pubmed/33414402 http://dx.doi.org/10.1038/s41398-020-01134-4 Text en © The Author(s) 2021 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
Frase, Lukas
Mertens, Lydia
Krahl, Arno
Bhatia, Kriti
Feige, Bernd
Heinrich, Sven P.
Vestring, Stefan
Nissen, Christoph
Domschke, Katharina
Bach, Michael
Normann, Claus
Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
title Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
title_full Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
title_fullStr Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
title_full_unstemmed Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
title_short Transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
title_sort transcranial direct current stimulation induces long-term potentiation-like plasticity in the human visual cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791098/
https://www.ncbi.nlm.nih.gov/pubmed/33414402
http://dx.doi.org/10.1038/s41398-020-01134-4
work_keys_str_mv AT fraselukas transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT mertenslydia transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT krahlarno transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT bhatiakriti transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT feigebernd transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT heinrichsvenp transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT vestringstefan transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT nissenchristoph transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT domschkekatharina transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT bachmichael transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex
AT normannclaus transcranialdirectcurrentstimulationinduceslongtermpotentiationlikeplasticityinthehumanvisualcortex