Cargando…

Understanding diaschisis models of attention dysfunction with rTMS

Visual attentive tracking requires a balance of excitation and inhibition across large-scale frontoparietal cortical networks. Using methods borrowed from network science, we characterize the induced changes in network dynamics following low frequency (1 Hz) repetitive transcranial magnetic stimulat...

Descripción completa

Detalles Bibliográficos
Autores principales: Garcia, Javier O., Battelli, Lorella, Plow, Ela, Cattaneo, Zaira, Vettel, Jean, Grossman, Emily D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483730/
https://www.ncbi.nlm.nih.gov/pubmed/32913263
http://dx.doi.org/10.1038/s41598-020-71692-6
_version_ 1783580955654488064
author Garcia, Javier O.
Battelli, Lorella
Plow, Ela
Cattaneo, Zaira
Vettel, Jean
Grossman, Emily D.
author_facet Garcia, Javier O.
Battelli, Lorella
Plow, Ela
Cattaneo, Zaira
Vettel, Jean
Grossman, Emily D.
author_sort Garcia, Javier O.
collection PubMed
description Visual attentive tracking requires a balance of excitation and inhibition across large-scale frontoparietal cortical networks. Using methods borrowed from network science, we characterize the induced changes in network dynamics following low frequency (1 Hz) repetitive transcranial magnetic stimulation (rTMS) as an inhibitory noninvasive brain stimulation protocol delivered over the intraparietal sulcus. When participants engaged in visual tracking, we observed a highly stable network configuration of six distinct communities, each with characteristic properties in node dynamics. Stimulation to parietal cortex had no significant impact on the dynamics of the parietal community, which already exhibited increased flexibility and promiscuity relative to the other communities. The impact of rTMS, however, was apparent distal from the stimulation site in lateral prefrontal cortex. rTMS temporarily induced stronger allegiance within and between nodal motifs (increased recruitment and integration) in dorsolateral and ventrolateral prefrontal cortex, which returned to baseline levels within 15 min. These findings illustrate the distributed nature by which inhibitory rTMS perturbs network communities and is preliminary evidence for downstream cortical interactions when using noninvasive brain stimulation for behavioral augmentations.
format Online
Article
Text
id pubmed-7483730
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-74837302020-09-15 Understanding diaschisis models of attention dysfunction with rTMS Garcia, Javier O. Battelli, Lorella Plow, Ela Cattaneo, Zaira Vettel, Jean Grossman, Emily D. Sci Rep Article Visual attentive tracking requires a balance of excitation and inhibition across large-scale frontoparietal cortical networks. Using methods borrowed from network science, we characterize the induced changes in network dynamics following low frequency (1 Hz) repetitive transcranial magnetic stimulation (rTMS) as an inhibitory noninvasive brain stimulation protocol delivered over the intraparietal sulcus. When participants engaged in visual tracking, we observed a highly stable network configuration of six distinct communities, each with characteristic properties in node dynamics. Stimulation to parietal cortex had no significant impact on the dynamics of the parietal community, which already exhibited increased flexibility and promiscuity relative to the other communities. The impact of rTMS, however, was apparent distal from the stimulation site in lateral prefrontal cortex. rTMS temporarily induced stronger allegiance within and between nodal motifs (increased recruitment and integration) in dorsolateral and ventrolateral prefrontal cortex, which returned to baseline levels within 15 min. These findings illustrate the distributed nature by which inhibitory rTMS perturbs network communities and is preliminary evidence for downstream cortical interactions when using noninvasive brain stimulation for behavioral augmentations. Nature Publishing Group UK 2020-09-10 /pmc/articles/PMC7483730/ /pubmed/32913263 http://dx.doi.org/10.1038/s41598-020-71692-6 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Garcia, Javier O.
Battelli, Lorella
Plow, Ela
Cattaneo, Zaira
Vettel, Jean
Grossman, Emily D.
Understanding diaschisis models of attention dysfunction with rTMS
title Understanding diaschisis models of attention dysfunction with rTMS
title_full Understanding diaschisis models of attention dysfunction with rTMS
title_fullStr Understanding diaschisis models of attention dysfunction with rTMS
title_full_unstemmed Understanding diaschisis models of attention dysfunction with rTMS
title_short Understanding diaschisis models of attention dysfunction with rTMS
title_sort understanding diaschisis models of attention dysfunction with rtms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483730/
https://www.ncbi.nlm.nih.gov/pubmed/32913263
http://dx.doi.org/10.1038/s41598-020-71692-6
work_keys_str_mv AT garciajaviero understandingdiaschisismodelsofattentiondysfunctionwithrtms
AT battellilorella understandingdiaschisismodelsofattentiondysfunctionwithrtms
AT plowela understandingdiaschisismodelsofattentiondysfunctionwithrtms
AT cattaneozaira understandingdiaschisismodelsofattentiondysfunctionwithrtms
AT vetteljean understandingdiaschisismodelsofattentiondysfunctionwithrtms
AT grossmanemilyd understandingdiaschisismodelsofattentiondysfunctionwithrtms