The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant

Inhibitory control relies on attention, inhibition, and other functions that are integrated across neural networks in an interactive manner. Functional MRI studies have provided excellent spatial mapping of the involved regions. However, finer temporal resolution is needed to capture the underlying...

Full description

Bibliographic Details
Main Authors: Joseph P. Happer, Laura C. Wagner, Lauren E. Beaton, Burke Q. Rosen, Ksenija Marinkovic
Format: Article
Language:English
Published: Elsevier 2021-05-01
Series:NeuroImage
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1053811921001142
id doaj-e4d44dd3686145b792860d55d29254f5
record_format Article
spelling doaj-e4d44dd3686145b792860d55d29254f52021-05-22T04:35:37ZengElsevierNeuroImage1095-95722021-05-01231117837The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variantJoseph P. Happer0Laura C. Wagner1Lauren E. Beaton2Burke Q. Rosen3Ksenija Marinkovic4San Diego State University/University of California, San Diego Joint Doctoral Program in Clinical Psychology, 5500 Campanile Dr., San Diego 92182, CA, United StatesDepartment of Psychology, San Diego State University, 5500 Campanile Dr., San Diego 92182, CA, United StatesDepartment of Psychology, San Diego State University, 5500 Campanile Dr., San Diego 92182, CA, United StatesDepartment of Psychology, San Diego State University, 5500 Campanile Dr., San Diego 92182, CA, United States; Department of Neurosciences, University of California, San Diego, 9500 Gilman Dr., La Jolla 92093, CA, United States; Corresponding author at: 6505 Alvarado Rd. Suite 202, San Diego 92120, CA, United States.San Diego State University/University of California, San Diego Joint Doctoral Program in Clinical Psychology, 5500 Campanile Dr., San Diego 92182, CA, United States; Department of Psychology, San Diego State University, 5500 Campanile Dr., San Diego 92182, CA, United States; Department of Radiology, University of California, San Diego, 9500 Gilman Dr., La Jolla 92093, CA, United StatesInhibitory control relies on attention, inhibition, and other functions that are integrated across neural networks in an interactive manner. Functional MRI studies have provided excellent spatial mapping of the involved regions. However, finer temporal resolution is needed to capture the underlying neural dynamics and the pattern of their functional contributions. Here, we used anatomically-constrained magnetoencephalography (aMEG) which combines MEG with structural MRI to examine how the spatial (“where”) and temporal (“when”) processing stages and interregional co-oscillations unfold in real time to contribute to inhibitory control. Healthy participants completed a modified Go/NoGo paradigm in which a subset of stimuli was modified to be visually salient (SAL). Compared to the non-modified condition, the SAL manipulation facilitated response withholding on NoGo trials and hindered responding to Go stimuli, reflecting attentional capture effectuated by an orienting response to SAL stimuli. aMEG source estimates indicate SAL stimuli elicited the attentional “circuit breaker” effect through early activity within a right-lateralized network centered around the lateral temporal cortex with additional activity in the pre-supplementary motor area (preSMA) and anterior insula (aINS/FO). Activity of the bilateral inferior frontal cortex responded specifically to inhibitory demands and was generally unaffected by the attentional manipulation. In contrast, early aINS/FO activity was sensitive to stimulus salience while subsequent activity was specific to inhibitory control. Activity estimated to the medial prefrontal cortex including the dorsal anterior cingulate cortex and preSMA reflected an integrative role that was sensitive to both inhibitory and attentional stimulus properties. At the level of neurofunctional networks, neural synchrony in the theta band (4–7 Hz) revealed interactions between principal cortical regions subserving attentional and inhibitory processes. Together, these results underscore the dynamic, integrative processing stages underlying inhibitory control.http://www.sciencedirect.com/science/article/pii/S1053811921001142Response inhibitionAttentionCognitive controlInferior frontal cortexMedial prefrontal cortexMagnetoencephalography
collection DOAJ
language English
format Article
sources DOAJ
author Joseph P. Happer
Laura C. Wagner
Lauren E. Beaton
Burke Q. Rosen
Ksenija Marinkovic
spellingShingle Joseph P. Happer
Laura C. Wagner
Lauren E. Beaton
Burke Q. Rosen
Ksenija Marinkovic
The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant
NeuroImage
Response inhibition
Attention
Cognitive control
Inferior frontal cortex
Medial prefrontal cortex
Magnetoencephalography
author_facet Joseph P. Happer
Laura C. Wagner
Lauren E. Beaton
Burke Q. Rosen
Ksenija Marinkovic
author_sort Joseph P. Happer
title The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant
title_short The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant
title_full The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant
title_fullStr The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant
title_full_unstemmed The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant
title_sort “when” and “where” of the interplay between attentional capture and response inhibition during a go/nogo variant
publisher Elsevier
series NeuroImage
issn 1095-9572
publishDate 2021-05-01
description Inhibitory control relies on attention, inhibition, and other functions that are integrated across neural networks in an interactive manner. Functional MRI studies have provided excellent spatial mapping of the involved regions. However, finer temporal resolution is needed to capture the underlying neural dynamics and the pattern of their functional contributions. Here, we used anatomically-constrained magnetoencephalography (aMEG) which combines MEG with structural MRI to examine how the spatial (“where”) and temporal (“when”) processing stages and interregional co-oscillations unfold in real time to contribute to inhibitory control. Healthy participants completed a modified Go/NoGo paradigm in which a subset of stimuli was modified to be visually salient (SAL). Compared to the non-modified condition, the SAL manipulation facilitated response withholding on NoGo trials and hindered responding to Go stimuli, reflecting attentional capture effectuated by an orienting response to SAL stimuli. aMEG source estimates indicate SAL stimuli elicited the attentional “circuit breaker” effect through early activity within a right-lateralized network centered around the lateral temporal cortex with additional activity in the pre-supplementary motor area (preSMA) and anterior insula (aINS/FO). Activity of the bilateral inferior frontal cortex responded specifically to inhibitory demands and was generally unaffected by the attentional manipulation. In contrast, early aINS/FO activity was sensitive to stimulus salience while subsequent activity was specific to inhibitory control. Activity estimated to the medial prefrontal cortex including the dorsal anterior cingulate cortex and preSMA reflected an integrative role that was sensitive to both inhibitory and attentional stimulus properties. At the level of neurofunctional networks, neural synchrony in the theta band (4–7 Hz) revealed interactions between principal cortical regions subserving attentional and inhibitory processes. Together, these results underscore the dynamic, integrative processing stages underlying inhibitory control.
topic Response inhibition
Attention
Cognitive control
Inferior frontal cortex
Medial prefrontal cortex
Magnetoencephalography
url http://www.sciencedirect.com/science/article/pii/S1053811921001142
work_keys_str_mv AT josephphapper thewhenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT lauracwagner thewhenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT laurenebeaton thewhenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT burkeqrosen thewhenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT ksenijamarinkovic thewhenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT josephphapper whenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT lauracwagner whenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT laurenebeaton whenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT burkeqrosen whenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
AT ksenijamarinkovic whenandwhereoftheinterplaybetweenattentionalcaptureandresponseinhibitionduringagonogovariant
_version_ 1721430933063598080