The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Regional brain activity when selecting a response despite interference: An H215O PET study of the stroop and an emotional stroop
Abstract
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 H 215 O 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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Studies of interference in serial verbal reactions
Stroop, J. R. (1935) · Journal of Experimental Psychology · doi:10.1037/h0054651 · Cited by 18,622
Cognitive Therapy of Depression
HOLLON, S. D., & BECK, A. T. (1979) · Cognitive-Behavioral Interventions · doi:10.1016/b978-0-12-404480-7.50012-5 · Cited by 4,685
Pardo, J. V., Pardo, P. J., Janer, K. W., & Raichle, M. E. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.1.256 · Cited by 1,495
The cingulate gyrus and human behaviour
Talairach, J., Bancaud, J., Geier, S., Bordas-Ferrer, M., Bonis, A., Szikla, G., & Rusu, M. (1973) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(73)90149-1 · Cited by 382
Mapping the functional neuroanatomy of the intact human brain with brain work imaging
Haxby, J. V., Grady, C. L., Ungerleider, L. G., & Horwitz, B. (1991) · Neuropsychologia · doi:10.1016/0028-3932(91)90009-w · Cited by 104
Self-citation
Cited by
Conflict monitoring and cognitive control
Botvinick, M. M., Braver, T. S., Barch, D. M., Carter, C. S., & Cohen, J. D. (2001) · Psychological Review · doi:10.1037/0033-295x.108.3.624 · Cited by 7,351
MacDonald, A. W., Cohen, J. D., Stenger, V. A., & Carter, C. S. (2000) · Science · doi:10.1126/science.288.5472.1835 · Cited by 3,666
Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies
Cabeza, R., & Nyberg, L. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137585 · Cited by 3,598
Common regions of the human frontal lobe recruited by diverse cognitive demands
Duncan, J., & Owen, A. M. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01633-7 · Cited by 2,498
Functional imaging of brain responses to pain. A review and meta-analysis (2000)
Peyron, R., Laurent, B., & García-Larrea, L. (2000) · Neurophysiologie Clinique/Clinical Neurophysiology · doi:10.1016/s0987-7053(00)00227-6 · Cited by 2,171
Nigg, J. T. (2000) · Psychological Bulletin · doi:10.1037/0033-2909.126.2.220 · Cited by 1,941
Niendam, T. A., Laird, A. R., Ray, K. L., Dean, Y. M., Glahn, D. C., & Carter, C. S. (2012) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-011-0083-5 · Cited by 1,700
Kober, H., Barrett, L. F., Joseph, J., Bliss-Moreau, E., Lindquist, K., & Wager, T. D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.059 · Cited by 1,144
Bush, G., Frazier, J. A., Rauch, S. L., Seidman, L. J., Whalen, P. J., Jenike, M. A., Rosen, B. R., & Biederman, J. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00083-9 · Cited by 866
The N2 in go/no-go tasks reflects conflict monitoring not response inhibition
Donkers, F. C. L., & van Boxtel, G. J. M. (2004) · Brain and Cognition · doi:10.1016/j.bandc.2004.04.005 · Cited by 749
Brain activity during transient sadness and happiness in healthy women
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.3.341 · Cited by 737
Posterior cingulate cortex activation by emotional words: fMRI evidence from a valence decision task
Maddock, R. J., Garrett, A. S., & Buonocore, M. H. (2003) · Human Brain Mapping · doi:10.1002/hbm.10075 · Cited by 695
Manly, T., Anderson, V., Nimmo‐Smith, I., Turner, A., Watson, P., & Robertson, I. H. (2001) · Journal of Child Psychology and Psychiatry · doi:10.1111/1469-7610.00806 · Cited by 693
MacLeod, C. M., & MacDonald, P. A. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01530-8 · Cited by 694
An ERP study of the temporal course of the Stroop color-word interference effect
Liotti, M., Woldorff, M. G., Perez, R., & Mayberg, H. S. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00106-2 · Cited by 653
Anterior cingulate cortex, conflict monitoring, and levels of processing
van Veen, V., Cohen, J. D., Botvinick, M. M., Stenger, V. A., & Carter, C. S. (2001) · NeuroImage · doi:10.1006/nimg.2001.0923 · Cited by 656
Whalen, P. J., Bush, G., McNally, R. J., Wilhelm, S., McInerney, S. C., Jenike, M. A., & Rauch, S. L. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00251-0 · Cited by 650
Brain imaging of the central executive component of working memory
Collette, F., & Van der Linden, M. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00063-x · Cited by 617
An fMRI study of anterior cingulate function in posttraumatic stress disorder
Shin, L. M., Whalen, P. J., Pitman, R. K., Bush, G., Macklin, M. L., Lasko, N. B., Orr, S. P., McInerney, S. C., & Rauch, S. L. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01215-x · Cited by 604
Brain generators of laser-evoked potentials: from dipoles to functional significance
Garcia-Larrea, L., Frot, M., & Valeriani, M. (2003) · Neurophysiologie Clinique/Clinical Neurophysiology · doi:10.1016/j.neucli.2003.10.008 · Cited by 541
Peterson, B. S., Skudlarski, P., Gatenby, J. C., Zhang, H., Anderson, A. W., & Gore, J. C. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00056-6 · Cited by 530
Milham, M. P., Banich, M. T., Webb, A., Barad, V, Cohen, N. J., Wszalek, T., & Kramer, A. F. (2001) · Cognitive Brain Research · doi:10.1016/s0926-6410(01)00076-3 · Cited by 521
Exploration of the neural substrates of executive functioning by functional neuroimaging
Collette, F., Hogge, M., Salmon, E., & Van der Linden, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.035 · Cited by 464
Exploring the unity and diversity of the neural substrates of executive functioning
Collette, F., Van der Linden, M., Laureys, S., Delfiore, G., Degueldre, C., Luxen, A., & Salmon, E. (2005) · Human Brain Mapping · doi:10.1002/hbm.20118 · Cited by 409
Casey, B. J., Thomas, K. M., Welsh, T. F., Badgaiyan, R. D., Eccard, C. H., Jennings, J. R., & Crone, E. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.15.8728 · Cited by 389
Self-citationLinguistic threat activates the human amygdala
Isenberg, N., Silbersweig, D., Engelien, A., Emmerich, S., Malavade, K., Beattie, B., Leon, A. C., & Stern, E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10456 · Cited by 378
Anterior cingulate cortex and response conflict: Effects of response modality and processing domain
Barch, D. M. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.9.837 · Cited by 359
Three key regions for supervisory attentional control: Evidence from neuroimaging meta-analyses
Cieslik, E. C., Mueller, V. I., Eickhoff, C. R., Langner, R., & Eickhoff, S. B. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.003 · Cited by 322
Bush, G., & Shin, L. M. (2006) · Nature Protocols · doi:10.1038/nprot.2006.48 · Cited by 309
The frontal aging hypothesis evaluated.
GREENWOOD, P. M. (2000) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617700666092 · Cited by 311
Milham, M. P., Banich, M. T., & Barad, V. (2003) · Cognitive Brain Research · doi:10.1016/s0926-6410(03)00108-3 · Cited by 299
Schroeter, M. L., Zysset, S., Kupka, T., Kruggel, F., & von Cramon, D. Y. (2002) · Human Brain Mapping · doi:10.1002/hbm.10052 · Cited by 259
Hsieh, J.-C., Ståhle-Bäckdahl, M., Hägermark, Ö., Stone-Elander, S., Rosenquist, G., & Ingvar, M. (1996) · Pain · doi:10.1016/0304-3959(95)00129-8 · Cited by 240
Bush, G., Spencer, T. J., Holmes, J., Shin, L. M., Valera, E. M., Seidman, L. J., Makris, N., Surman, C., Aleardi, M., Mick, E., et al. (2008) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2007.16 · Cited by 201
Neural basis of the emotional Stroop interference effect in major depression
Mitterschiffthaler, M. T., Williams, S. C. R., Walsh, N. D., Cleare, A. J., Donaldson, C., Scott, J., & Fu, C. H. Y. (2008) · Psychological Medicine · doi:10.1017/s0033291707001523 · Cited by 190
Event-related potentials during an emotional Stroop task
Thomas, S. J., Johnstone, S. J., & Gonsalvez, C. J. (2007) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2006.10.002 · Cited by 190
The Constraints Functional Neuroimaging Places on Classical Models of Auditory Word Processing
Giraud, A. L., & Price, C. J. (2001) · Journal of Cognitive Neuroscience · doi:10.1162/08989290152541421 · Cited by 163
Noel, X. (2002) · Alcohol and Alcoholism · doi:10.1093/alcalc/37.4.347 · Cited by 153
Cerebral metabolic dysfunction and impaired vigilance in recently abstinent methamphetamine abusers
London, E. D., Berman, S. M., Voytek, B., Simon, S. L., Mandelkern, M. A., Monterosso, J., Thompson, P. M., Brody, A. L., Geaga, J. A., Hong, M. S., et al. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.04.039 · Cited by 136
Badzakova-Trajkov, G., Barnett, K. J., Waldie, K. E., & Kirk, I. J. (2009) · Brain Research · doi:10.1016/j.brainres.2008.11.069 · Cited by 121
A Double Dissociation Between Mood States and Personality Traits in the Anterior Cingulate.
Canli, T., Amin, Z., Haas, B., Omura, K., & Constable, R. T. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.897 · Cited by 92
Feng, C., Becker, B., Huang, W., Wu, X., Eickhoff, S. B., & Chen, T. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.023 · Cited by 58
The Impact of Emotional States on Cognitive Control Circuitry and Function
Cohen, A. O., Dellarco, D. V., Breiner, K., Helion, C., Heller, A. S., Rahdar, A., Pedersen, G., Chein, J., Dyke, J. P., Galvan, A., et al. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00906 · Cited by 54
Self-citationKubicki, M., Niznikiewicz, M., Connor, E., Ungar, L., Nestor, P. G., Bouix, S., Dreusicke, M., Kikinis, R., McCarley, R. W., & Shenton, M. E. (2009) · Brain Imaging and Behavior · doi:10.1007/s11682-009-9061-8 · Cited by 38
Mier, D., Bailer, J., Ofer, J., Kerstner, T., Zamoscik, V., Rist, F., Witthöft, M., & Diener, C. (2017) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.160081 · Cited by 20
Metadata
- Authors
- George, M. S., Ketter, T. A., Parekh, P. I., Rosinsky, N., Ring, H., Casey, B. J., Trimble, M. R., Horwitz, B., Herscovitch, P., & Post, R. M.
- Venue
- Human Brain Mapping
- Publisher
- Wiley
- Published
- 1994-01
- Volume
- 1
- Issue
- 3
- Pages
- 194-209
- ISSN
- 1065-9471 (ISSN-L)
- 1097-0193
- OpenAlex
- W1994473322
- Cited by
- 252
- References
- 5
- FWCI
- 11.19
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.