Cargando…

The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex

Measuring the brain’s response to transcranial magnetic stimulation (TMS) with electroencephalography (EEG) offers unique insights into the cortical circuits activated following stimulation, particularly in non-motor regions where less is known about TMS physiology. However, the mechanisms underlyin...

Descripción completa

Detalles Bibliográficos
Autores principales: Rogasch, Nigel C., Zipser, Carl, Darmani, Ghazaleh, Mutanen, Tuomas P., Biabani, Mana, Zrenner, Christoph, Desideri, Debora, Belardinelli, Paolo, Müller-Dahlhaus, Florian, Ziemann, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035341/
https://www.ncbi.nlm.nih.gov/pubmed/32081901
http://dx.doi.org/10.1038/s41598-020-59911-6
_version_ 1783500048445734912
author Rogasch, Nigel C.
Zipser, Carl
Darmani, Ghazaleh
Mutanen, Tuomas P.
Biabani, Mana
Zrenner, Christoph
Desideri, Debora
Belardinelli, Paolo
Müller-Dahlhaus, Florian
Ziemann, Ulf
author_facet Rogasch, Nigel C.
Zipser, Carl
Darmani, Ghazaleh
Mutanen, Tuomas P.
Biabani, Mana
Zrenner, Christoph
Desideri, Debora
Belardinelli, Paolo
Müller-Dahlhaus, Florian
Ziemann, Ulf
author_sort Rogasch, Nigel C.
collection PubMed
description Measuring the brain’s response to transcranial magnetic stimulation (TMS) with electroencephalography (EEG) offers unique insights into the cortical circuits activated following stimulation, particularly in non-motor regions where less is known about TMS physiology. However, the mechanisms underlying TMS-evoked EEG potentials (TEPs) remain largely unknown. We assessed TEP sensitivity to changes in excitatory neurotransmission mediated by n-methyl-d-aspartate (NMDA) receptors following stimulation of non-motor regions. In fourteen male volunteers, resting EEG and TEPs from prefrontal (PFC) and parietal (PAR) cortex were measured before and after administration of either dextromethorphan (NMDA receptor antagonist) or placebo across two sessions in a double-blinded pseudo-randomised crossover design. At baseline, there were amplitude differences between PFC and PAR TEPs across a wide time range (15–250 ms), however the signals were correlated after ~80 ms, suggesting early peaks reflect site-specific activity, whereas late peaks reflect activity patterns less dependent on the stimulated sites. Early TEP peaks were not reliably altered following dextromethorphan compared to placebo, although findings were less clear for later peaks, and low frequency resting oscillations were reduced in power. Our findings suggest that early TEP peaks (<80 ms) from PFC and PAR reflect stimulation site specific activity that is largely insensitive to changes in NMDA receptor-mediated neurotransmission.
format Online
Article
Text
id pubmed-7035341
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70353412020-02-28 The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex Rogasch, Nigel C. Zipser, Carl Darmani, Ghazaleh Mutanen, Tuomas P. Biabani, Mana Zrenner, Christoph Desideri, Debora Belardinelli, Paolo Müller-Dahlhaus, Florian Ziemann, Ulf Sci Rep Article Measuring the brain’s response to transcranial magnetic stimulation (TMS) with electroencephalography (EEG) offers unique insights into the cortical circuits activated following stimulation, particularly in non-motor regions where less is known about TMS physiology. However, the mechanisms underlying TMS-evoked EEG potentials (TEPs) remain largely unknown. We assessed TEP sensitivity to changes in excitatory neurotransmission mediated by n-methyl-d-aspartate (NMDA) receptors following stimulation of non-motor regions. In fourteen male volunteers, resting EEG and TEPs from prefrontal (PFC) and parietal (PAR) cortex were measured before and after administration of either dextromethorphan (NMDA receptor antagonist) or placebo across two sessions in a double-blinded pseudo-randomised crossover design. At baseline, there were amplitude differences between PFC and PAR TEPs across a wide time range (15–250 ms), however the signals were correlated after ~80 ms, suggesting early peaks reflect site-specific activity, whereas late peaks reflect activity patterns less dependent on the stimulated sites. Early TEP peaks were not reliably altered following dextromethorphan compared to placebo, although findings were less clear for later peaks, and low frequency resting oscillations were reduced in power. Our findings suggest that early TEP peaks (<80 ms) from PFC and PAR reflect stimulation site specific activity that is largely insensitive to changes in NMDA receptor-mediated neurotransmission. Nature Publishing Group UK 2020-02-21 /pmc/articles/PMC7035341/ /pubmed/32081901 http://dx.doi.org/10.1038/s41598-020-59911-6 Text en © The Author(s) 2020 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
Rogasch, Nigel C.
Zipser, Carl
Darmani, Ghazaleh
Mutanen, Tuomas P.
Biabani, Mana
Zrenner, Christoph
Desideri, Debora
Belardinelli, Paolo
Müller-Dahlhaus, Florian
Ziemann, Ulf
The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex
title The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex
title_full The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex
title_fullStr The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex
title_full_unstemmed The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex
title_short The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex
title_sort effects of nmda receptor blockade on tms-evoked eeg potentials from prefrontal and parietal cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035341/
https://www.ncbi.nlm.nih.gov/pubmed/32081901
http://dx.doi.org/10.1038/s41598-020-59911-6
work_keys_str_mv AT rogaschnigelc theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT zipsercarl theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT darmanighazaleh theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT mutanentuomasp theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT biabanimana theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT zrennerchristoph theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT desideridebora theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT belardinellipaolo theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT mullerdahlhausflorian theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT ziemannulf theeffectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT rogaschnigelc effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT zipsercarl effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT darmanighazaleh effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT mutanentuomasp effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT biabanimana effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT zrennerchristoph effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT desideridebora effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT belardinellipaolo effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT mullerdahlhausflorian effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex
AT ziemannulf effectsofnmdareceptorblockadeontmsevokedeegpotentialsfromprefrontalandparietalcortex