Cargando…

Cortical modulation of short-latency TMS-evoked potentials

Transcranial magnetic stimulation–electroencephalogram (TMS–EEG) co-registration offers the opportunity to test reactivity of brain areas across distinct conditions through TMS-evoked potentials (TEPs). Several TEPs have been described, their functional meaning being largely unknown. In particular,...

Descripción completa

Detalles Bibliográficos
Autores principales: Veniero, Domenica, Bortoletto, Marta, Miniussi, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540821/
https://www.ncbi.nlm.nih.gov/pubmed/23316155
http://dx.doi.org/10.3389/fnhum.2012.00352
_version_ 1782255263619743744
author Veniero, Domenica
Bortoletto, Marta
Miniussi, Carlo
author_facet Veniero, Domenica
Bortoletto, Marta
Miniussi, Carlo
author_sort Veniero, Domenica
collection PubMed
description Transcranial magnetic stimulation–electroencephalogram (TMS–EEG) co-registration offers the opportunity to test reactivity of brain areas across distinct conditions through TMS-evoked potentials (TEPs). Several TEPs have been described, their functional meaning being largely unknown. In particular, short-latency potentials peaking at 5 (P5) and 8 (N8) ms after the TMS pulse have been recently described, but because of their large amplitude, the problem of whether their origin is cortical or not has been opened. To gain information about these components, we employed a protocol that modulates primary motor cortex excitability (MI): low frequency stimulation of premotor area (PMC). TMS was applied simultaneously with EEG recording from 70 electrodes. Amplitude of TEPs evoked by 200 single-pulses TMS delivered over MI at 110% of resting motor threshold (rMT) was measured before and after applying 900 TMS conditioning stimuli to left PMC with 1 Hz repetition rate. Single subject analyses showed reduction in TEPs amplitude after PMC conditioning in a sample of participants and increase in TEPs amplitude in two subjects. No effects were found on corticospinal excitability as recorded by motor-evoked potentials (MEPs). Furthermore, correlation analysis showed an inverse relation between the effects of the conditioning protocol on P5-N8 complex amplitude and MEPs amplitude. Because the effects of the used protocol have been ascribed to a cortical interaction between premotor area and MI, we suggest that despite the sign of P5-N8 amplitude modulation is not consistent across participant; this modulation could indicate, at least in part, their cortical origin. We conclude that with an accurate experimental procedure early latency components can be used to evaluate the reactivity of the stimulated cortex.
format Online
Article
Text
id pubmed-3540821
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-35408212013-01-11 Cortical modulation of short-latency TMS-evoked potentials Veniero, Domenica Bortoletto, Marta Miniussi, Carlo Front Hum Neurosci Neuroscience Transcranial magnetic stimulation–electroencephalogram (TMS–EEG) co-registration offers the opportunity to test reactivity of brain areas across distinct conditions through TMS-evoked potentials (TEPs). Several TEPs have been described, their functional meaning being largely unknown. In particular, short-latency potentials peaking at 5 (P5) and 8 (N8) ms after the TMS pulse have been recently described, but because of their large amplitude, the problem of whether their origin is cortical or not has been opened. To gain information about these components, we employed a protocol that modulates primary motor cortex excitability (MI): low frequency stimulation of premotor area (PMC). TMS was applied simultaneously with EEG recording from 70 electrodes. Amplitude of TEPs evoked by 200 single-pulses TMS delivered over MI at 110% of resting motor threshold (rMT) was measured before and after applying 900 TMS conditioning stimuli to left PMC with 1 Hz repetition rate. Single subject analyses showed reduction in TEPs amplitude after PMC conditioning in a sample of participants and increase in TEPs amplitude in two subjects. No effects were found on corticospinal excitability as recorded by motor-evoked potentials (MEPs). Furthermore, correlation analysis showed an inverse relation between the effects of the conditioning protocol on P5-N8 complex amplitude and MEPs amplitude. Because the effects of the used protocol have been ascribed to a cortical interaction between premotor area and MI, we suggest that despite the sign of P5-N8 amplitude modulation is not consistent across participant; this modulation could indicate, at least in part, their cortical origin. We conclude that with an accurate experimental procedure early latency components can be used to evaluate the reactivity of the stimulated cortex. Frontiers Media S.A. 2013-01-09 /pmc/articles/PMC3540821/ /pubmed/23316155 http://dx.doi.org/10.3389/fnhum.2012.00352 Text en Copyright © 2013 Veniero, Bortoletto and Miniussi. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Veniero, Domenica
Bortoletto, Marta
Miniussi, Carlo
Cortical modulation of short-latency TMS-evoked potentials
title Cortical modulation of short-latency TMS-evoked potentials
title_full Cortical modulation of short-latency TMS-evoked potentials
title_fullStr Cortical modulation of short-latency TMS-evoked potentials
title_full_unstemmed Cortical modulation of short-latency TMS-evoked potentials
title_short Cortical modulation of short-latency TMS-evoked potentials
title_sort cortical modulation of short-latency tms-evoked potentials
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540821/
https://www.ncbi.nlm.nih.gov/pubmed/23316155
http://dx.doi.org/10.3389/fnhum.2012.00352
work_keys_str_mv AT venierodomenica corticalmodulationofshortlatencytmsevokedpotentials
AT bortolettomarta corticalmodulationofshortlatencytmsevokedpotentials
AT miniussicarlo corticalmodulationofshortlatencytmsevokedpotentials