Cited by 624Motor Control and AdaptationNeural and Behavioral Psychology StudiesSport Psychology and Performance

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Anatomy of Motor Learning. I. Frontal Cortex and Attention to Action

Jueptner, M., Stephan, K. M., Frith, C. D., Brooks, D. J., Frackowiak, R.S.J., Passingham, R. E.·1997·Journal of Neurophysiology

DOI 10.1152/jn.1997.77.3.1313

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Abstract

We used positron emission tomography to study new learning and automatic performance in normal volunteers. Subjects learned sequences of eight finger movements by trial and error. In a previous experiment we showed that the prefrontal cortex was activated during new learning but not during during automatic performance. The aim of the present experiment was to see what areas could be reactivated if the subjects performed the prelearned sequence but were required to pay attention to what they were doing. Scans were carried out under four conditions. In the first the subjects performed a prelearned sequence of eight key presses; this sequence was learned before scanning and was practiced until it had become overlearned, so that the subjects were able to perform it automatically. In the second condition the subjects learned a new sequence during scanning. In a third condition the subjects performed the prelearned sequence, but they were required to attend to what they were doing; they were instructed to think about the next movement. The fourth condition was a baseline condition. As in the earlier study, the dorsal prefrontal cortex and anterior cingulate area 32 were activated during new learning, but not during automatic performance. The left dorsal prefrontal cortex and the right anterior cingulate cortex were reactivated when subjects paid attention to the performance of the prelearned sequence compared with automatic performance of the same task. It is suggested that the critical feature was that the subjects were required to attend to the preparation of their responses. However, the dorsal prefrontal cortex and the anterior cingulate cortex were activated more when the subjects learned a new sequence than they were when subjects simply paid attention to a prelearned sequence. New learning differs from the attention condition in that the subjects generated moves, monitored the outcomes, and remembered the responses that had been successful. All these are nonroutine operations to which the subjects must attend. Further analysis is needed to specify which are the nonroutine operations that require the involvement of the dorsal prefrontal and anterior cingulate cortex.

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The assessment and analysis of handedness: The Edinburgh inventory
Oldfield, R. C. (1971) · Neuropsychologia · doi:10.1016/0028-3932(71)90067-4 · Cited by 35,900
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
The attention system of the human brain
Posner, M. I., & Petersen, S. E. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.000325 · Cited by 8,070 · cited 1×
“Posner and Petersen (1990) have necessary to specify what operations must be performed that are nonroutine.reviewed other evidence from PET that the anterior cingulate cortex plays an important role in attention to action.”
Background
Attention to Action: Willed and Automatic Control of Behavior
Norman, D. A., & Shallice, T. (1986) · Consciousness and Self-Regulation · doi:10.1007/978-1-4757-0629-1_1 · Cited by 4,455
Large-scale neurocognitive networks and distributed processing for attention, language, and memory
Mesulam, M. (1990) · Annals of Neurology · doi:10.1002/ana.410280502 · Cited by 2,684
Rapid Automated Algorithm for Aligning and Reslicing PET Images
Woods, R. P., Cherry, S. R., & Mazziotta, J. C. (1992) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199207000-00024 · Cited by 1,901
Comparing Functional (PET) Images: The Assessment of Significant Change
Friston, K. J., Frith, C., Liddle, P. F., & Frackowiak, R. S. J. (1991) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1991.122 · Cited by 1,626
A PET study of visuospatial attention
Corbetta, M., Miezin, F. M., Shulman, G., & Petersen, S. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-03-01202.1993 · Cited by 1,604
Practice-related Changes in Human Brain Functional Anatomy during Nonmotor Learning
Raichle, M. E., Fiez, J. A., Videen, T. O., MacLeod, A.-M. K., Pardo, J. V., Fox, P. T., & Petersen, S. E. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.1.8 · Cited by 1,593
The anterior cingulate cortex mediates processing selection in the Stroop attentional conflict paradigm
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

Show all 38 references

Research works printed but not linked: 1

Vogt B. A., 1992, Cereb. Cortex, 2, 435

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Kalayam, B., & Alexopoulos, G. S. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.8.713 · Cited by 263
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Motor Memory Consolidation in Sleep Shapes More Effective Neuronal Representations
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Authors: Jueptner, M., Stephan, K. M., Frith, C. D., Brooks, D. J., Frackowiak, R. S. J., & Passingham, R. E.
Affiliations: Hammersmith Hospital (GB)
ORCID: Frith, C. D.
Brooks, D. J.
Frackowiak, R.S.J.
Venue: Journal of Neurophysiology
Publisher: American Physiological Society
Published: 1997-03-01
Volume: 77
Issue: 3
Pages: 1313-1324
ISSN: 0022-3077 (ISSN-L)
1522-1598
DOI: 10.1152/jn.1997.77.3.1313
OpenAlex: W2219528871
Cited by: 624
References: 38
Citations by year: 2026: 2 · 2025: 7 · 2024: 9 · 2023: 9 · 2022: 11 · 2021: 17 · 2020: 16 · 2019: 9 · 2018: 13 · 2017: 19 · 2016: 25 · 2015: 18 · 2014: 23 · 2013: 29 · 2012: 20
FWCI: 19.28
Type: journal article
Language: en
Open access: closed
Locations: Journal of Neurophysiology (publishedVersion)
PubMed (publishedVersion)
Funders: Wellcome Trust
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Social Sciences › Psychology › Developmental and Educational Psychology › Sport Psychology and Performance
Keywords: motor learning, prefrontal cortex, dorsal prefrontal cortex, anterior cingulate cortex, overlearning, response preparation, trial-and-error learning, brain activation
MeSH terms: Adult, Attention, Cerebrovascular Circulation, Fingers, Humans, Learning, Magnetic Resonance Imaging, Male, Psychomotor Performance, Tomography, Emission-Computed, Prefrontal Cortex

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Anatomy of Motor Learning. I. Frontal Cortex and Attention to Action

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