Cited by 123Motor Control and AdaptationNeuroscience and Music PerceptionNeural and Behavioral Psychology Studies

Human cerebellum plays an important role in memory-timed finger movement: an fMRI study

Kawashima, Ryuta, Okuda, Jiro, Umetsu, Atsushi, Sugiura, Motoaki, Inoue, Kentaro, Suzuki, Kyoko, Tabuchi, Michio, Tsukiura, Takashi +7 more·2000·Journal of Neurophysiology

Abstract

The purpose of this study was to determine, by using functional magnetic resonance imaging, the areas of the brain activated during a memory-timed finger movement task and compare these with those activated during a visually cued movement task. Because it is likely that subjects engage in subvocalization associated with chronometric counting to achieve accurate timing during memory-timed movements, the authors sought to determine the areas of the brain activated during a silent articulation task in which the subjects were instructed to reproduce the same timing as for the memory-timed movement task without any lip movements or vocalization. The memory-timed finger movement task induced activation of the anterior lobe of the cerebellum (lobules IV and V) bilaterally, the contralateral primary motor area, the supplementary motor area (SMA), the premotor area (PMA), the prefrontal cortex, and the posterior parietal cortex bilaterally, compared with the resting condition. The same areas in the SMA and left prefrontal cortex were activated during the silent articulation task compared with the resting condition. The anterior lobe of the cerebellum on both sides was also activated during the silent articulation task compared with the resting condition, but these activations did not reach statistical significance (P < 0.05 corrected). In addition, the anterior cerebellum on both sides showed significant activation during the memory-timed movement task when compared with the visually cued finger movement task. The visually cued finger movement task specifically activated the ipsilateral PMA and the intraparietal cortex bilaterally. The results indicate that the anterior lobe of the cerebellum of both sides, the SMA, and the left prefrontal cortex were probably involved in the generation of accurate timing, functioning as a clock within the CNS, and that the dorsal visual pathway may be involved in the generation of visually cued movements.

Integrity signals

Registry

Crossref · 10.1152/jn.2000.83.2.1079

Cites

64 of 64 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The contribution of the SMA and bilateral anterior cerebellum to overt picture naming, vocalisation, and breathing occurs prior to vocalisation.

    “Activation in the SMA and bilateral anterior cerebellum (lobules IV and V) during silent articulation tasks (Kawashima et al., 2000) suggested that the contribution of these regions to other tasks such as overt picture naming (Etard et al., 2000), vocalisation (Hirano et al., 1997) and breathing (Murphy et al., 1997) occurred prior to vocalisation.”
  • The SMA and bilateral anterior cerebellum (lobules IV and V) are activated during silent articulation tasks.

    “Activation in the SMA and bilateral anterior cerebellum (lobules IV and V) during silent articulation tasks (Kawashima et al., 2000) suggested that the contribution of these regions to other tasks such as overt picture naming (Etard et al., 2000), vocalisation (Hirano et al., 1997) and breathing (Murphy et al., 1997) occurred prior to vocalisation.”
  • The SMA plays a role in the timing of speech and nonspeech motor commands.

    “A role for the SMA in the timing of speech and nonspeech motor commands was suggested following observations that the SMA was activated during silent articulation and memory-timed finger movements (Kawashima et al., 2000).”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Kawashima, R., Okuda, J., Umetsu, A., Sugiura, M., Inoue, K., Suzuki, K., Tabuchi, M., Tsukiura, T., Narayan, S. L., Nagasaka, T., Yanagawa, I., Fujii, T., Takahashi, S., Fukuda, H., & Yamadori, A.
Affiliations
  • Tohoku University (JP)
  • Tohoku University Hospital (JP)
Venue
Journal of Neurophysiology
Published
2000-02-01
Volume
83
Issue
2
Pages
1079-1087
ISSN
  • 0022-3077 (ISSN-L)
  • 1522-1598
OpenAlex
W2143845140
Cited by
123
References
64
Citations by year
2025: 3 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 4 · 2016: 2 · 2015: 2 · 2014: 3 · 2013: 6 · 2012: 9
FWCI
5.18
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Neurophysiology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords
cerebellum, movement timing, subvocalization, supplementary motor area, prefrontal cortex, premotor cortex, intraparietal cortex, dorsal visual pathway, internal clock, motor control
MeSH terms
Adult, Cerebellum, Fingers, Humans, Magnetic Resonance Imaging, Male, Memory, Movement, Psychomotor Performance, Time Perception, Prefrontal Cortex

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