The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Memory of Learning Facilitates Saccadic Adaptation in the Monkey
Open accessAbstract
A motor learning mechanism called saccadic adaptation ensures accuracy of saccades throughout life despite growth, aging, and some pathologies of the oculomotor plant or nervous system. The present study investigates effects of preceding adaptation on the speed of subsequent adaptation during single experiments. Adaptive changes in gain (movement size divided by target eccentricity) were induced by intrasaccadic step (ISS) of the target. After the gain was altered (control block), we reversed the direction of ISS to bring the gain back to approximately 1.0 (recovery). We then reversed ISS direction again to induce another adaptation (test block). Analyses revealed that the gain changed at a higher rate in the early part of test adaptation than in the corresponding part of control. After approximately 100-300 saccades in the test block, adaptation slowed down. The gain value at which adaptation slowed was correlated with the gain achieved in the control. We further examined effects of a 30 min intervention inserted between recovery and test blocks. When zero-visual-error trials ( approximately 700 saccades) were repeated during this period, the rate of test adaptation was similar to that of control. In contrast, when the animal was deprived of visual inputs during this period, test adaptation was still influenced by preceding learning. We conclude that a memory of previous learning remains during recovery to facilitate subsequent adaptation and that such a memory does not disappear merely with time but is erased actively by repeated zero-error movements. Our results, which cannot be explained by a single mechanism, suggest that the saccadic system is equipped with more than one plasticity process.
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“In particular, relearning of a given perturbation for a second time is faster than initial learning – a phenomenon known as savings (Ebbinghaus, 1913; Kojima et al., 2004; Krakauer et al., 2005; Smith et al., 2006; Zarahn et al., 2008) – whereas a basic single-timescale SSM predicts that learning should always occur at the same rate, regardless of past experience (Zarahn et al., 2008).”
From Rethinking motor learning and savings in adaptation paradigms: model-free memory for successful actions combines with internal models (2011) · cites this paper as Kojima et al., 2004
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Cites
A method for measuring horizontal and vertical eye movement chronically in the monkey.
Fuchs, A. F., & Robinson, D. A. (1966) · Journal of Applied Physiology · doi:10.1152/jappl.1966.21.3.1068 · Cited by 795 · cited 2×
“Two rhesus monkeys (Macaca mulatta, male; 4.5 and 6.8 kg) were prepared for eye movement recording by the magnetic search coil method (Fuchs and Robinson, 1966).”
MethodInfluentialCerebellar-dependent adaptive control of primate saccadic system
Optican, L. M., & Robinson, D. A. (1980) · Journal of Neurophysiology · doi:10.1152/jn.1980.44.6.1058 · Cited by 773 · cited 2×
“The oculo - motor vermis and the fastigial oculomotor region ( FOR ) of the cerebellum have been shown to be key players in saccadic adap - tation ( Optican and Robinson , 1980 ; Takagi et al .”
BackgroundParametric adjustment in saccadic eye movements
McLaughlin, S. C. (1967) · Perception & Psychophysics · doi:10.3758/bf03210071 · Cited by 570 · cited 3×
“Adaptive changes in saccade amplitude were induced by a conventional intrasaccadic target step paradigm (McLaughlin, 1967).”
BackgroundMethodEffects of Lesions of the Oculomotor Vermis on Eye Movements in Primate: Saccades
Takagi, M., Zee, D. S., & Tamargo, R. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.4.1911 · Cited by 374 · cited 1×
“The oculomotor vermis and the fastigial oculomotor region (FOR) of the cerebellum have been shown to be key players in saccadic adaptation (Optican and Robinson, 1980; Takagi et al., 1998; Barash et al., 1999; Scudder, 2002; Inaba et al., 2003; Scudder and McGee, 2003).”
BackgroundLev‐Ram, V., Wong, S. T., Storm, D. R., & Tsien, R. Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122206399 · Cited by 330 · cited 1×
“Recent results describe a previously unrecognized form of long-term potentiation in the cerebellar cortex (Lev-Ram et al., 2002) and a synaptic depotentiation in the hippocampus (Montgomery and Madison, 2002).”
BackgroundThe characteristics and neuronal substrate of saccadic eye movement plasticity
Hopp, J. J., & Fuchs, A. F. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.12.002 · Cited by 316 · cited 1×
“This is because the saccadic gain (saccade amplitude divided by target eccentricity) is constantly recalibrated by a learning mechanism called saccadic adaptation (for review, see Hopp and Fuchs, 2004).”
BackgroundSaccadic Dysmetria and Adaptation after Lesions of the Cerebellar Cortex
Barash, S., Melikyan, A., Sivakov, A., Zhang, M., Glickstein, M., & Thier, P. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-24-10931.1999 · Cited by 312 · cited 1×
“The oculomotor vermis and the fastigial oculomotor region (FOR) of the cerebellum have been shown to be key players in saccadic adaptation (Optican and Robinson, 1980; Takagi et al., 1998; Barash et al., 1999; Scudder, 2002; Inaba et al., 2003; Scudder and McGee, 2003).”
BackgroundA Mechanism for Savings in the Cerebellum
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“In the subsequent recovery block, the cortical plasticity decreases back to and possibly beyond the preadaptation level, as has been suggested for the extinction of eye blink conditioning (Medina et al., 2001), but the nuclear plasticity remains potentiated.”
BackgroundSaccadic Gain Modification: Visual Error Drives Motor Adaptation
Wallman, J., & Fuchs, A. F. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.5.2405 · Cited by 218 · cited 2×
“There is good evidence that saccadic adaptation is a form of motor learning driven by visual error immediately after the end of saccades (Wallman and Fuchs, 1998; Shafer et al., 2000; Noto and Robinson, 2001).”
BackgroundCharacteristics of Saccadic Gain Adaptation in Rhesus Macaques
Straube, A. M., Fuchs, A. F., Usher, S., & Robinson, F. R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.2.874 · Cited by 211 · cited 6×
“Adaptation is fairly specific to the amplitude and direction of adapted saccades and does not generalize fully to those with different vectors (Straube et al., 1997; Wallman and Fuchs, 1998; Noto et al., 1999; Watanabe et al., 2000).”
BackgroundInfluential
Research works printed but not linked: 5
- 2003, Soc Neurosci Abstr, 29, 441.7
- 2003, Neurosci Res, 46, S159
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Cited by
Sorted by citations
Error Correction, Sensory Prediction, and Adaptation in Motor Control
Shadmehr, R., Smith, M. A., & Krakauer, J. W. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153135 · Cited by 1,869
“This phenomenon has been observed in a wide range of paradigms (Rescorla, 2004;Kojima et al., 2004;Stollhoff et al., 2005).”
BackgroundPrinciples of sensorimotor learning
Wolpert, D. M., Diedrichsen, J., & Flanagan, J. R. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3112 · Cited by 1,391
“A recent model 79 based on this idea of temporal credit assignment can account for a number of phenomena that are related to reach movement adaptation to perturbations as well as saccadic adaptation 98 .”
BackgroundInteracting adaptive processes with different timescales underlie short-term motor learning
Smith, M. A., Ghazizadeh, A., & Shadmehr, R. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040179 · Cited by 1,113
“observed in their saccade adaptation experiment following a period of darkness [3].”
BackgroundKrakauer, J. W., Hadjiosif, A. M., Xu, J., Wong, A. L., & Haith, A. M. (2019) · Comprehensive physiology · doi:10.1002/cphy.c170043 · Cited by 918
Krakauer, J. W., & Shadmehr, R. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2005.10.003 · Cited by 516
Metadata
- Authors
- Kojima, Y., Iwamoto, Y., & Yoshida, K.
- Affiliations
- University of Tsukuba (JP)
- Corresponding author
- Iwamoto, Yoshiki
- ORCID
- Kojima, Yoshiko
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-08-25
- Volume
- 24
- Issue
- 34
- Pages
- 7531-7539
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6729647
- OpenAlex
- W2096184857
- Cited by
- 179
- References
- 31
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 5 · 2023: 9 · 2022: 6 · 2021: 15 · 2020: 19 · 2019: 18 · 2018: 5 · 2017: 5 · 2016: 7 · 2015: 13 · 2014: 11 · 2013: 8 · 2012: 5
- FWCI
- 2.35
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (13680894)
- 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
- saccadic adaptation, motor learning, visual deprivation
- MeSH terms
- Adaptation, Ocular, Animals, Learning, Macaca mulatta, Male, Memory, Saccades
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