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Common and distinct neural mechanisms of attentional switching and response conflict

Producción científica: Articlerevisión exhaustiva

25 Citas (Scopus)

Resumen

The human capacities for overcoming prepotent actions and flexibly switching between tasks represent cornerstones of cognitive control. Functional neuroimaging has implicated a diverse set of brain regions contributing to each of these cognitive control processes. However, the extent to which attentional switching and response conflict draw on shared or distinct neural mechanisms remains unclear. The current study examined the neural correlates of response conflict and attentional switching using event-related functional magnetic resonance imaging (fMRI) and a fully randomized 2×2 design. We manipulated an arrow-word version of the Stroop task to measure conflict and switching in the context of a single task decision, in response to a common set of stimuli. Under these common conditions, both behavioral and imaging data showed significant main effects of conflict and switching but no interaction. However, conjunction analyses identified frontal regions involved in both switching and response conflict, including the dorsal anterior cingulate cortex (dACC) and left inferior frontal junction. In addition, connectivity analyses demonstrated task-dependent functional connectivity patterns between dACC and inferior temporal cortex for attentional switching and between dACC and posterior parietal cortex for response conflict. These results suggest that the brain makes use of shared frontal regions, but can dynamically modulate the connectivity patterns of some of those regions, to deal with attentional switching and response conflict.

Idioma originalEnglish
Páginas (desde-hasta)92-102
Número de páginas11
PublicaciónBrain Research
Volumen1469
DOI
EstadoPublished - ago 21 2012

Nota bibliográfica

Funding Information:
This study was supported by NIA Grant R01 AG033036 and NSF Grant BCS-0814302 . We thank Sara Cilles for help in recruiting and scheduling subjects.

Financiación

This study was supported by NIA Grant R01 AG033036 and NSF Grant BCS-0814302 . We thank Sara Cilles for help in recruiting and scheduling subjects.

FinanciadoresNúmero del financiador
National Science Foundation (NSF)BCS-0814302
National Institute on AgingR01AG033036

    ASJC Scopus subject areas

    • General Neuroscience
    • Molecular Biology
    • Clinical Neurology
    • Developmental Biology

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