An Essential Role of the Intraparietal Sulcus in Response Inhibition Predicted by Parcellation-Based Network.
cortical parcellation
executive function
posterior parietal cortex
response inhibition
transcranial magnetic stimulation
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
ISSN: 1529-2401
Titre abrégé: J Neurosci
Pays: United States
ID NLM: 8102140
Informations de publication
Date de publication:
27 03 2019
27 03 2019
Historique:
received:
30
08
2018
revised:
28
12
2018
accepted:
04
01
2019
pubmed:
30
1
2019
medline:
19
3
2020
entrez:
30
1
2019
Statut:
ppublish
Résumé
The posterior parietal cortex (PPC) features close anatomical and functional relationships with the prefrontal cortex. However, the necessity of the PPC in executive functions has been questioned. The present study used the stop-signal task to examine response inhibition, an executive function that inhibits prepotent response tendency. The brain activity and resting-state functional connectivity were measured to analyze a parcellation-based network that was aimed at identifying a candidate PPC region essential for response inhibition in humans. The intraparietal sulcus (IPS) was activated during response inhibition and connected with the inferior frontal cortex and the presupplementary motor area, the two frontal regions known to be necessary for response inhibition. Next, transcranial magnetic stimulation (TMS) was used to test the essential role of the IPS region for response inhibition. TMS over the IPS region prolonged the stop-signal reaction time (SSRT), the standard behavioral index used to evaluate stopping performance, when stimulation was applied 30-0 ms before stopping. On the contrary, stimulation over the temporoparietal junction region, an area activated during response inhibition but lacking connectivity with the two frontal regions, did not show changes in SSRT. These results indicate that the IPS identified using the parcellation-based network plays an essential role in executive functions.
Identifiants
pubmed: 30692225
pii: JNEUROSCI.2244-18.2019
doi: 10.1523/JNEUROSCI.2244-18.2019
pmc: PMC6435821
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2509-2521Informations de copyright
Copyright © 2019 the authors 0270-6474/19/392509-13$15.00/0.
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