Inactivation of the central thalamus delays self-timed saccades
Open accessAbstract
The central thalamus transmits corollary discharge signals for eye movement control, but its role in eye movement generation remains uncertain. Inactivation of the paralaminar part of the ventrolateral thalamus delayed the initiation of contraversive saccades, particularly during a new memory-guided saccade task that required self-triggering of the movement. The results suggest that signals through the thalamus regulate the timing of self-initiated saccades.
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Corollary discharge has repeatedly been implicated in the process of updating the internal record of the current saccade to facilitate planning the next.
“CD has repeatedly been implicated in this process59–64.”
From Corollary discharge across the animal kingdom (2008) · cites this paper as [64]
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Basal ganglia and cerebellar loops: motor and cognitive circuits
Middleton, F. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00040-5 · Cited by 1,940 · see citing works
Lewis, P. A., & Miall, R. C. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00036-9 · Cited by 837 · see citing works
The neural representation of time
Ivry, R. B., & Spencer, R. M. C. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.013 · Cited by 827 · see citing works
Hikosaka, O., & Wurtz, R. H. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1268 · Cited by 697 · see citing works
The thalamostriatal system: a highly specific network of the basal ganglia circuitry
Smith, Y., Raju, D. V., Paré, J., & Sidibé, M. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.07.004 · Cited by 595 · see citing works
A Pathway in Primate Brain for Internal Monitoring of Movements
Sommer, M. A., & Wurtz, R. H. (2002) · Science · doi:10.1126/science.1069590 · Cited by 565 · see citing works
McFarland, N. R., & Haber, S. N. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-08117.2002 · Cited by 496 · see citing works
Martin, J. H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90784-q · Cited by 459 · see citing works
Schlag-Rey, M., & Schlag, J. (1984) · Journal of Neurophysiology · doi:10.1152/jn.1984.51.6.1149 · Cited by 184 · see citing works
Involvement of the Central Thalamus in the Control of Smooth Pursuit Eye Movements
Tanaka, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0676-05.2005 · Cited by 99 · see citing works
Self-citationvan Donkelaar, P., Stein, J. F., Passingham, R. E., & Miall, R. C. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2780 · Cited by 84 · see citing works
Wyder, M. T., Massoglia, D. P., & Stanford, T. R. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00064.2003 · Cited by 82 · see citing works
Wyder, M. T., Massoglia, D. P., & Stanford, T. R. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01221.2003 · Cited by 64 · see citing works
Watanabe, Y., & Funahashi, S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00995.2003 · Cited by 60 · see citing works
Tanibuchi, I., & Goldman‐Rakic, P. S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00969.2003 · Cited by 32 · see citing works
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Research works printed but not linked: 1
- Olszewski, J. The thalamus of the Macaca mulatta: An atlas for use with the stereotaxic instrument. (Karger, Basel, Switzerland, 1952).
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- Authors
- Tanaka, M.
- Affiliations
- Hokkaido University (JP)
- Corresponding author
- Tanaka, Masaki
- ORCID
- Tanaka, Masaki
- Venue
- Nature Neuroscience
- Published
- 2005-12-11
- Volume
- 9
- Issue
- 1
- Pages
- 20-22
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2061325097
- Cited by
- 54
- References
- 15
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 5 · 2023: 1 · 2021: 5 · 2020: 2 · 2019: 2 · 2018: 4 · 2017: 5 · 2016: 5 · 2015: 2 · 2014: 1 · 2013: 4 · 2012: 2
- FWCI
- 0.82
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Institutional Repositories DataBase (IRDB) (submittedVersion)
- Hokkaido University Collection of Scholarly and Academic Papers (Hokkaido University) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
- Keywords
- central thalamus, ventrolateral thalamic nucleus, saccade timing, memory-guided saccades, corollary discharge, oculomotor control, saccade initiation
- MeSH terms
- Animals, Haplorhini, Basal Ganglia, Cerebral Cortex, Fixation, Ocular, Memory, Photic Stimulation, Saccades, Thalamus, Ventral Thalamic Nuclei
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