Regional brain activity when selecting a response despite interference: An H2 15O PET study of the stroop and an emotional stroop
Corresponding Author
M. S. George
MD
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
NIMH, Bldg 10, Rm 3N212, 9000 Rockville Pike, Bethesda, MD 20892Search for more papers by this authorT. A. Ketter
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorP. I. Parekh
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorN. Rosinsky
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorH. Ring
Raymond Way Neuropsychiatry Research Group, Institute of Neurology, Queen Square, London, United Kingdom
Search for more papers by this authorB. J. Casey
Child Psychiatry Branch, NIMH, NIH, Bethesda, Maryland
Search for more papers by this authorM. R. Trimble
Raymond Way Neuropsychiatry Research Group, Institute of Neurology, Queen Square, London, United Kingdom
Search for more papers by this authorB. Horwitz
Laboratory of Neurosciences, National Institute of Aging, NIH, Bethesda, Maryland
Search for more papers by this authorP. Herscovitch
Positron Emission Tomography Section, Department of Nuclear Medicine, NIH, Bethesda, Maryland
Search for more papers by this authorR. M. Post
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorCorresponding Author
M. S. George
MD
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
NIMH, Bldg 10, Rm 3N212, 9000 Rockville Pike, Bethesda, MD 20892Search for more papers by this authorT. A. Ketter
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorP. I. Parekh
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorN. Rosinsky
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorH. Ring
Raymond Way Neuropsychiatry Research Group, Institute of Neurology, Queen Square, London, United Kingdom
Search for more papers by this authorB. J. Casey
Child Psychiatry Branch, NIMH, NIH, Bethesda, Maryland
Search for more papers by this authorM. R. Trimble
Raymond Way Neuropsychiatry Research Group, Institute of Neurology, Queen Square, London, United Kingdom
Search for more papers by this authorB. Horwitz
Laboratory of Neurosciences, National Institute of Aging, NIH, Bethesda, Maryland
Search for more papers by this authorP. Herscovitch
Positron Emission Tomography Section, Department of Nuclear Medicine, NIH, Bethesda, Maryland
Search for more papers by this authorR. M. Post
Biological Psychiatry Branch, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Bethesda, Maryland
Search for more papers by this authorAbstract
The Stroop interference test requires a person to respond to specific elements of a stimulus while suppressing a competing response. Previous positron emission tomography (PET) work has shown increased activity in the right anterior cingulate gyrus during the Stroop test. It is unclear, however, whether the anterior cingulate participates more in the attentional rather than the response selection aspects of the task or whether different interference stimuli might activate different brain regions. We sought to determine (1) whether the Stroop interference task causes increased activation in the right anterior cingulate as previously reported, (2) whether this activation varied as a function of response time, (3) what brain regions were functionally linked to the cingulate during performance of the Stroop, and (4) whether a modified Stroop task involving emotionally distracting words would activate the cingulate and other limbic and paralimbic regions. Twenty-one healthy volunteers were scanned with H215O PET while they performed the Stroop interference test (standard Stroop), a modified Stroop task using distracting words with sad emotional content (sad Stroop), and a control task of naming colors. These were presented in a manner designed to maximize the response selection aspects of the task. Images were stereotactically normalized and analyzed using statistical parametric mapping (SPM). Predictably, subjects were significantly slower during the standard Stroop than the sad Stroop or the control task. The left mideingulate region robustly activated during the standard Stroop compared to the control task. The sad Stroop activated this same region, but to a less significant degree. Correlational regional network analysis revealed an inverse relationship between activation in the left mideingulate and the left insula and temporal lobe. Additionally, activity in different regions of the cingulate gyrus correlated with performance speed during the standard Stroop. These results suggest that the left midcingulate is likely to be part of a neural network activated when one attempts to override a competing verbal response. Finally, the left midcingulate region appears to be functionally coupled to the left insula, temporal, and frontal cortex during cognitive interference tasks involving language. These results underscore the important role of the cingulate gyrus in selecting appropriate and suppressing inappropriate verbal responses. © 1994 Wiley-Liss, Inc.
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