JN Information on EB 2010
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 77: 1099-1118, 1997;
0022-3077/97 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (17)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Marsh, E.
Right arrow Articles by Baker, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Marsh, E.
Right arrow Articles by Baker, R.

The Journal of Neurophysiology Vol. 77 No. 3 March 1997, pp. 1099-1118
Copyright ©1997 The American Physiological Society

Normal and Adapted Visuooculomotor Reflexes in Goldfish

Eric Marsh and Robert Baker

Department of Physiology and Neuroscience, New York University Medical Center, New York 10016

Marsh, Eric and Robert Baker. Normal and adapted visuooculomotor reflexes in goldfish. J. Neurophysiol. 77: 1099-1118. Under normal physiological conditions, whole field visual motion generally occurs in response to either active or passive self-motion. In the laboratory, selective movement of the visual surround produces an optokinetic response (OKR) that acts primarily to support the vestibuloocular reflex (VOR). During visual world motion, however, the OKR can be viewed as operating independently over frequency and amplitude ranges insufficient for vestibular activation. The goal of the present study was to characterize this isolated behavior of the OKR in goldfish as an essential step for studying central neuronal correlates of visual-vestibular interactions and the mechanisms underlying oculomotor adaptation. After presentation of either binocular sinusoidal or step visual stimuli, conjugate eye movements were elicited with an amplitude and phase profile similar to that of other vertebrates. An early and a delayed component were measured with different dynamics that could be altered independently by visual training. The ensuing visuomotor plasticity was robust and exhibited five major characteristics. First, the gain of both early and delayed components of the OKR increased >100%. Second, eye velocity decreased 0.5-2.0 s before the change in direction of stimulus velocity. Third, on lengthening the duration of a constant velocity visual stimulus (e.g., from 8 to 16 s), eye velocity decreased toward 0°/s. This behavior was correlated with the direction and period as opposed to the frequency of the visual stimulus ("period tuning"). Fourth, visual stimulus training increased VOR eye velocity with a ratio of 0.6 to 1 to that measured for the OKR. Fifth, after OKR adaptation, eye velocity consistently oscillated in a conjugate, symmetrical fashion at 2.4 Hz in the light, whereas in the dark, a rhythmical low-amplitude eye velocity occurred at the visual training frequency. We conclude that the frequency and amplitude of visual stimuli for eliciting the goldfish OKR are well suited for complementing the VOR. Unlike most mammals, OKR adaptive modifications significantly alter VOR gain, whereas the effects of VOR training are much less on OKR gain. These observations suggest that both distributed circuits and discrete neuronal populations control visuo- and vestibulomotor performance. Finally, the existence of a rhythmic, "period tuned" visuomotor behavior provides a unique opportunity to examine the neuronal mechanisms of adaptive plasticity.




This article has been cited by other articles:


Home page
J. Neurosci.Home page
R. R. Kimpo and J. L. Raymond
Impaired Motor Learning in the Vestibulo-Ocular Reflex in Mice with Multiple Climbing Fiber Input to Cerebellar Purkinje Cells
J. Neurosci., May 23, 2007; 27(21): 5672 - 5682.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Straka, J. C. Beck, A. M. Pastor, and R. Baker
Morphology and Physiology of the Cerebellar Vestibulolateral Lobe Pathways Linked to Oculomotor Function in the Goldfish
J Neurophysiol, October 1, 2006; 96(4): 1963 - 1980.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. C. Beck, P. Rothnie, H. Straka, S. L. Wearne, and R. Baker
Precerebellar Hindbrain Neurons Encoding Eye Velocity During Vestibular and Optokinetic Behavior in the Goldfish
J Neurophysiol, September 1, 2006; 96(3): 1370 - 1382.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. C. Beck, E. Gilland, D. W. Tank, and R. Baker
Quantifying the Ontogeny of Optokinetic and Vestibuloocular Behaviors in Zebrafish, Medaka, and Goldfish
J Neurophysiol, December 1, 2004; 92(6): 3546 - 3561.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. Major, R. Baker, E. Aksay, B. Mensh, H. S. Seung, and D. W. Tank
Plasticity and tuning by visual feedback of the stability of a neural integrator
PNAS, May 18, 2004; 101(20): 7739 - 7744.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. Major, R. Baker, E. Aksay, H. S. Seung, and D. W. Tank
Plasticity and tuning of the time course of analog persistent firing in a neural integrator
PNAS, May 18, 2004; 101(20): 7745 - 7750.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Katoh, H. Kitazawa, S. Itohara, and S. Nagao
Dynamic characteristics and adaptability of mouse vestibulo-ocular and optokinetic response eye movements and the role of the flocculo-olivary system revealed by chemical lesions
PNAS, June 23, 1998; 95(13): 7705 - 7710.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online