Cargando…
Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study
Over the past few years, the possibility of modulating fast brain oscillatory activity in the gamma (γ) band through transcranial alternating current stimulation (tACS) has been discussed in the context of both cognitive enhancement and therapeutic scenarios. However, the effects of tACS targeting r...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308536/ https://www.ncbi.nlm.nih.gov/pubmed/35880231 http://dx.doi.org/10.1155/2022/6197505 |
_version_ | 1784753002600464384 |
---|---|
author | Mencarelli, Lucia Monti, Lucia Romanella, Sara Neri, Francesco Koch, Giacomo Salvador, Ricardo Ruffini, Giulio Sprugnoli, Giulia Rossi, Simone Santarnecchi, Emiliano |
author_facet | Mencarelli, Lucia Monti, Lucia Romanella, Sara Neri, Francesco Koch, Giacomo Salvador, Ricardo Ruffini, Giulio Sprugnoli, Giulia Rossi, Simone Santarnecchi, Emiliano |
author_sort | Mencarelli, Lucia |
collection | PubMed |
description | Over the past few years, the possibility of modulating fast brain oscillatory activity in the gamma (γ) band through transcranial alternating current stimulation (tACS) has been discussed in the context of both cognitive enhancement and therapeutic scenarios. However, the effects of tACS targeting regions outside the motor cortex, as well as its spatial specificity, are still unclear. Here, we present a concurrent tACS-fMRI block design study to characterize the impact of 40 Hz tACS applied over the left and right dorsolateral prefrontal cortex (DLPFC) in healthy subjects. Results suggest an increase in blood oxygenation level-dependent (BOLD) activity in the targeted bilateral DLPFCs, as well as in surrounding brain areas affected by stimulation according to biophysical modeling, i.e., the premotor cortex and anterior cingulate cortex (ACC). However, off-target effects were also observed, primarily involving the visual cortices, with further effects on the supplementary motor areas (SMA), left subgenual cingulate, and right superior temporal gyrus. The specificity of 40 Hz tACS over bilateral DLPFC and the possibility for network-level effects should be considered in future studies, especially in the context of recently promoted gamma-induction therapeutic protocols for neurodegenerative disorders. |
format | Online Article Text |
id | pubmed-9308536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-93085362022-07-24 Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study Mencarelli, Lucia Monti, Lucia Romanella, Sara Neri, Francesco Koch, Giacomo Salvador, Ricardo Ruffini, Giulio Sprugnoli, Giulia Rossi, Simone Santarnecchi, Emiliano Neural Plast Research Article Over the past few years, the possibility of modulating fast brain oscillatory activity in the gamma (γ) band through transcranial alternating current stimulation (tACS) has been discussed in the context of both cognitive enhancement and therapeutic scenarios. However, the effects of tACS targeting regions outside the motor cortex, as well as its spatial specificity, are still unclear. Here, we present a concurrent tACS-fMRI block design study to characterize the impact of 40 Hz tACS applied over the left and right dorsolateral prefrontal cortex (DLPFC) in healthy subjects. Results suggest an increase in blood oxygenation level-dependent (BOLD) activity in the targeted bilateral DLPFCs, as well as in surrounding brain areas affected by stimulation according to biophysical modeling, i.e., the premotor cortex and anterior cingulate cortex (ACC). However, off-target effects were also observed, primarily involving the visual cortices, with further effects on the supplementary motor areas (SMA), left subgenual cingulate, and right superior temporal gyrus. The specificity of 40 Hz tACS over bilateral DLPFC and the possibility for network-level effects should be considered in future studies, especially in the context of recently promoted gamma-induction therapeutic protocols for neurodegenerative disorders. Hindawi 2022-07-16 /pmc/articles/PMC9308536/ /pubmed/35880231 http://dx.doi.org/10.1155/2022/6197505 Text en Copyright © 2022 Lucia Mencarelli et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mencarelli, Lucia Monti, Lucia Romanella, Sara Neri, Francesco Koch, Giacomo Salvador, Ricardo Ruffini, Giulio Sprugnoli, Giulia Rossi, Simone Santarnecchi, Emiliano Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study |
title | Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study |
title_full | Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study |
title_fullStr | Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study |
title_full_unstemmed | Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study |
title_short | Local and Distributed fMRI Changes Induced by 40 Hz Gamma tACS of the Bilateral Dorsolateral Prefrontal Cortex: A Pilot Study |
title_sort | local and distributed fmri changes induced by 40 hz gamma tacs of the bilateral dorsolateral prefrontal cortex: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308536/ https://www.ncbi.nlm.nih.gov/pubmed/35880231 http://dx.doi.org/10.1155/2022/6197505 |
work_keys_str_mv | AT mencarellilucia localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT montilucia localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT romanellasara localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT nerifrancesco localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT kochgiacomo localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT salvadorricardo localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT ruffinigiulio localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT sprugnoligiulia localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT rossisimone localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy AT santarnecchiemiliano localanddistributedfmrichangesinducedby40hzgammatacsofthebilateraldorsolateralprefrontalcortexapilotstudy |