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Role of the Lateral Prefrontal Cortex in Executive Behavioral Control
Abstract
The lateral prefrontal cortex is critically involved in broad aspects of executive behavioral control. Early studies emphasized its role in the short-term retention of information retrieved from cortical association areas and in the inhibition of prepotent responses. Recent studies of subhuman primates and humans have revealed the role of this area in more general aspects of behavioral planning. Novel findings of neuronal activity have specified how neurons in this area take part in selective attention for action and in selecting an intended action. Furthermore, the involvement of the lateral prefrontal cortex in the implementation of behavioral rules and in setting multiple behavioral goals has been discovered. Recent studies have begun to reveal neuronal mechanisms for strategic behavioral planning and for the development of knowledge that enables the planning of macrostructures of event-action sequences at the conceptual level.
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Cites
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
Neural Mechanisms of Selective Visual Attention
Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685
DEFICITS IN STRATEGY APPLICATION FOLLOWING FRONTAL LOBE DAMAGE IN MAN
SHALLICE, T., & BURGESS, P. W. (1991) · Brain · doi:10.1093/brain/114.2.727 · Cited by 2,017
Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960
‘What’ and ‘where’ in the human brain
Ungerleider, L. G., & Haxby, J. V. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90066-3 · Cited by 1,913
Temporal dynamics of brain activation during a working memory task
Cohen, J. D., Perlstein, W. M., Braver, T. S., Nystrom, L. E., Noll, D. C., Jonides, J., & Smith, E. E. (1997) · Nature · doi:10.1038/386604a0 · Cited by 1,876
Behavioral Theories and the Neurophysiology of Reward
Schultz, W. (2006) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070229 · Cited by 1,637
Modulation of memory fields by dopamine Dl receptors in prefrontal cortex
Williams, G. V., & Goldman-Rakic, P. S. (1995) · Nature · doi:10.1038/376572a0 · Cited by 1,593
Dissociation in prefrontal cortex of affective and attentional shifts
Dias, R., Robbins, T. W., & Roberts, A. C. (1996) · Nature · doi:10.1038/380069a0 · Cited by 1,527
Multiple reward signals in the brain
Schultz, W. (2000) · Nature Reviews Neuroscience · doi:10.1038/35044563 · Cited by 1,303
Overlapping mechanisms of attention and spatial working memory
Awh, E., & Jonides, J. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01593-x · Cited by 1,229
Amygdalo‐cortical projections in the monkey ( Macaca fascicularis )
Amaral, D. G., & Price, J. L. (1984) · Journal of Comparative Neurology · doi:10.1002/cne.902300402 · Cited by 1,162
Categorical Representation of Visual Stimuli in the Primate Prefrontal Cortex
Freedman, D. J., Riesenhuber, M., Poggio, T., & Miller, E. K. (2001) · Science · doi:10.1126/science.291.5502.312 · Cited by 1,123
A neural basis for visual search in inferior temporal cortex
Chelazzi, L., Miller, E. K., Duncan, J., & Desimone, R. (1993) · Nature · doi:10.1038/363345a0 · Cited by 1,114
Petrides, M., & Pandya, D. N. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00518.x · Cited by 1,068
Neural correlates of a decision in the dorsolateral prefrontal cortex of the macaque
Kim, J.-N., & Shadlen, M. N. (1999) · Nature Neuroscience · doi:10.1038/5739 · Cited by 950
Intelligence and the Frontal Lobe: The Organization of Goal-Directed Behavior
Duncan, J., Emslie, H., Williams, P., Johnson, R., & Freer, C. (1996) · Cognitive Psychology · doi:10.1006/cogp.1996.0008 · Cited by 902
Petrides, M., & Pandya, D. N. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2001.02090.x · Cited by 882
An adaptive coding model of neural function in prefrontal cortex
Duncan, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35097575 · Cited by 874
Response suppression, initiation and strategy use following frontal lobe lesions
Burgess, P. W., & Shallice, T. (1996) · Neuropsychologia · doi:10.1016/0028-3932(95)00104-2 · Cited by 854
The orbitofrontal cortex: Neuronal activity in the behaving monkey
Thorpe, S. J., Rolls, E. T., & Maddison, S. (1983) · Experimental Brain Research · doi:10.1007/bf00235545 · Cited by 836
Neuronal correlates of parametric working memory in the prefrontal cortex
Romo, R., Brody, C. D., Hernández, A., & Lemus, L. (1999) · Nature · doi:10.1038/20939 · Cited by 822
Neural organization for the long-term memory of paired associates
Sakai, K., & Miyashita, Y. (1991) · Nature · doi:10.1038/354152a0 · Cited by 743
Responses of Neurons in Inferior Temporal Cortex During Memory-Guided Visual Search
Chelazzi, L., Duncan, J., Miller, E. K., & Desimone, R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.6.2918 · Cited by 726
Human prefrontal cortex: processing and representational perspectives
Wood, J. N., & Grafman, J. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1033 · Cited by 721
Reward expectancy in primate prefrental neurons
Watanabe, M. (1996) · Nature · doi:10.1038/382629a0 · Cited by 684
Prefrontal cortex and decision making in a mixed-strategy game
Barraclough, D. J., Conroy, M. L., & Lee, D. (2004) · Nature Neuroscience · doi:10.1038/nn1209 · Cited by 678
Architectonic subdivision of the orbital and medial prefrontal cortex in the macaque monkey
Carmichael, S. T., & Price, J. L. (1994) · Journal of Comparative Neurology · doi:10.1002/cne.903460305 · Cited by 656
Arnsten, A. F. T., & Goldman-Rakic, P. S. (1985) · Science · doi:10.1126/science.2999977 · Cited by 549
Lau, H. C., Rogers, R. D., Haggard, P., & Passingham, R. E. (2004) · Science · doi:10.1126/science.1090973 · Cited by 539
Are the frontal lobes implicated in “planning” functions? Interpreting data from the Tower of Hanoi
Goel, V., & Grafman, J. (1995) · Neuropsychologia · doi:10.1016/0028-3932(95)90866-p · Cited by 510
NEURAL SELECTION AND CONTROL OF VISUALLY GUIDED EYE MOVEMENTS
Schall, J. D., & Thompson, K. G. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.241 · Cited by 489
Anatomic Organization of the Basilar Pontine Projections from Prefrontal Cortices in Rhesus Monkey
Schmahmann, J. D., & Pandya, D. N. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00438.1997 · Cited by 461
Leon, M. I., & Shadlen, M. N. (1999) · Neuron · doi:10.1016/s0896-6273(00)80854-5 · Cited by 449
Prospective coding for objects in primate prefrontal cortex
Rainer, G., Rao, S. C., & Miller, E. K. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05493.1999 · Cited by 432
Russchen, F. T., Amaral, D. G., & Price, J. L. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902560202 · Cited by 416
Organization of the nigrothalamocortical system in the rhesus monkey
Ilinsky, I. A., Jouandet, M. L., & Goldman‐Rakic, P. S. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902360304 · Cited by 406
Transient activation of inferior prefrontal cortex during cognitive set shifting
Konishi, S., Nakajima, K., Uchida, I., Kameyama, M., Nakahara, K., Sekihara, K., & Miyashita, Y. (1998) · Nature Neuroscience · doi:10.1038/283 · Cited by 401
Neural Circuits Subserving the Retrieval and Maintenance of Abstract Rules
Bunge, S. A., Kahn, I., Wallis, J. D., Miller, E. K., & Wagner, A. D. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00910.2002 · Cited by 361
Fractionating Attentional Control Using Event-Related fMRI
Hampshire, A., & Owen, A. M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj116 · Cited by 329
Projections from the amygdala to basoventral and mediodorsal prefrontal regions in the rhesus monkey
Barbas, H., & de Olmos, J. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.903000409 · Cited by 324
Decomposing components of task preparation with functional magnetic resonance imaging.
Brass, M., & Cramon, D. Y. V. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/089892904323057335 · Cited by 302
Diverse thalamic projections to the prefrontal cortex in the rhesus monkey
Barbas, H., Henion, T. H. H., & Dermon, C. R. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903130106 · Cited by 292
Functional MRI of macaque monkeys performing a cognitive set-shifting task
Nakahara, K., Hayashi, T., Konishi, S., & Miyashita, Y. (2002) · Science · doi:10.1126/science.1067653 · Cited by 286
Williams, S. M., & Goldman-Rakic, P. S. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.3.199 · Cited by 284
Specialisation within the prefrontal cortex: the ventral prefrontal cortex and associative learning
Passingham, R. E., Toni, I., & Rushworth, M. F. S. (2000) · Experimental Brain Research · doi:10.1007/s002210000405 · Cited by 268
Activity in the lateral prefrontal cortex reflects multiple steps of future events in action plans
Mushiake, H., Saito, N., Sakamoto, K., Itoyama, Y., & Tanji, J. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.045 · Cited by 249
Self-citationSingle cell activity in ventral prefrontal cortex of behaving monkeys
Rosenkilde, C. E., Bauer, R. H., & Fuster, J. M. (1981) · Brain Research · doi:10.1016/0006-8993(81)90160-8 · Cited by 233
Filtering of neural signals by focused attention in the monkey prefrontal cortex
Everling, S., Tinsley, C. J., Gaffan, D., & Duncan, J. (2002) · Nature Neuroscience · doi:10.1038/nn874 · Cited by 224
Predicting events of varying probability: uncertainty investigated by fMRI
Volz, K. G., Schubotz, R. I., & von Cramon, D. Y. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00122-8 · Cited by 214
Smiley, J. F., & Goldman-Rakic, P. S. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.3.223 · Cited by 211
THE FRONTAL LOBE IN MAN: A CLINICAL STUDY OF MAXIMUM REMOVALS
PENFIELD, W., & EVANS, J. (1935) · Brain · doi:10.1093/brain/58.1.115 · Cited by 193
Lidow, M. S., Goldman‐Rakic, P. S., Gallager, D. W., & Rakic, P. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902800104 · Cited by 77
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Coding and use of tactile signals from the fingertips in object manipulation tasks
Johansson, R. S., & Flanagan, J. R. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2621 · Cited by 2,063
The role of prefrontal cortex in cognitive control and executive function
Friedman, N. P., & Robbins, T. W. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01132-0 · Cited by 1,737
“The following sections selectively survey findings from the enormous literature on these issues (see also reviews by Tanji & Hoshi [68] and Badre [69]).”
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Graybiel, A. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112851 · Cited by 1,697
Is the rostro-caudal axis of the frontal lobe hierarchical?
Badre, D., & D'Esposito, M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2667 · Cited by 946
Neural computations underlying arbitration between model-based and model-free learning
Lee, S. W., Shimojo, S., & O’Doherty, J. P. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.028 · Cited by 642
Metadata
- Authors
- Tanji, J., & Hoshi, E.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2008-01
- Volume
- 88
- Issue
- 1
- Pages
- 37-57
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2160545525
- Cited by
- 447
- References
- 55
- FWCI
- 1.80
- Type
- journal article
- Language
- en
- Open access
- closed
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