Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (10)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by MacAskill, M. R.
Right arrow Articles by Jones, R. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by MacAskill, M. R.
Right arrow Articles by Jones, R. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 125, No. 7, 1570-1582, July 2002
© 2002 Guarantors of Brain

Adaptive modification of saccade amplitude in Parkinson’s disease

Michael R. MacAskill1,2, Tim J. Anderson1,2,3 and Richard D. Jones1,2,4

1 Christchurch Movement Disorders and Brain Research Group, 2 Department of Medicine, Christchurch School of Medicine and Health Sciences, 3 Department of Neurology and 4 Department of Medical Physics and Bioengineering, Christchurch Hospital, Christchurch, New Zealand

Correspondence to: Michael R. MacAskill, Department of Medicine, Christchurch School of Medicine, PO Box 4345, Christchurch, New Zealand E-mail: michael.macaskill{at}chmeds.ac.nz

The accuracy of saccades (fast eye movements) is maintained over time and is an adaptive ability usually ascribed to the cerebellum. Adaptation might occur elsewhere in certain tasks, such as in the prefrontal cortex for memory-guided saccades. We hypothesized that adaptation of memory-guided saccades would be impaired in Parkinson’s disease, as basal ganglia dysfunction can disrupt the operation of the prefrontal cortex, while adaptation of visually guided saccades would be preserved. Adaptation was induced by consistently yet imperceptibly displacing targets as saccades were made toward them, causing artificial saccadic inaccuracy. Twelve Parkinson’s disease subjects (OFF medication) and 12 age-matched controls performed 245 visually- and memory-guided horizontal saccades in separate sessions. An infrared eye tracker detected the saccade, during which the target was displaced by 12.5% of the size of the initial jump, either in the same (centrifugal) or the opposite (centripetal) direction. Parkinson’s disease subjects made smaller visually guided saccades than did controls [F(1,20) = 9.10, P < 0.01], yet both groups modified saccade size appropriately. Parkinson’s disease memory-guided saccades were also smaller than those of controls [F(1,19) = 5.93, P < 0.05]. While controls decreased (by 8.6%) or increased (by 4.1%) the size of these saccades appropriately, Parkinson’s disease subjects decreased saccade size in response to both centripetal adaptation (by an excessive 18.3%) and centrifugal adaptation (by 3.5%). Parkinson’s disease subjects were less able to modify saccadic size appropriately when the movement size was specified in motor memory: a predilection for excessive hypometria was invoked, regardless of adaptation direction. This indicates that, in certain tasks, saccadic adaptation involves structures other than the cerebellum.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Ann. N. Y. Acad. Sci.Home page
M. VERSINO, C. ZAVANONE, S. COLNAGHI, G. BELTRAMI, C. PACCHETTI, R. ZANGAGLIA, and V. COSI
Binocular Control of Saccades in Idiopathic Parkinson's Disease
Ann. N.Y. Acad. Sci., April 1, 2005; 1039(1): 588 - 592.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. W. Krakauer, M.-F. Ghilardi, M. Mentis, A. Barnes, M. Veytsman, D. Eidelberg, and C. Ghez
Differential Cortical and Subcortical Activations in Learning Rotations and Gains for Reaching: A PET Study
J Neurophysiol, February 1, 2004; 91(2): 924 - 933.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
V. Biousse, B. C. Skibell, R. L. Watts, D. N. Loupe, C. Drews-Botsch, and N. J. Newman
Ophthalmologic features of Parkinson's disease
Neurology, January 27, 2004; 62(2): 177 - 180.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.