JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 89: 2528-2537, 2003. First published January 15, 2003; doi:10.1152/jn.01055.2002
0022-3077/03 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
89/5/2528    most recent
01055.2002v1
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 ISI 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 ISI Web of Science (18)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lee, I. H.
Right arrow Articles by Assad, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lee, I. H.
Right arrow Articles by Assad, J. A.

J Neurophysiol (May 1, 2003). 10.1152/jn.01055.2002
Submitted on Submitted 21 November 2002; accepted in final form 14 January 2003

Putaminal Activity for Simple Reactions or Self-Timed Movements

Irwin H. Lee and John A. Assad

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115

Lee, Irwin H. and John A. Assad. Putaminal Activity for Simple Reactions or Self-Timed Movements. J. Neurophysiol. 89: 2528-2537, 2003. To examine the role of basal ganglia-cortical circuits in movement initiation, we trained monkeys to make the same arm movements in two ways---in immediate reaction to a randomly timed external cue (cued movements) and also following a variable delay without an explicit initiation signal (self-timed movements). The two movement types were interleaved and balanced in overall timing to allow a direct comparison of activity before and during the movement. Posterior putaminal neurons generally had phasic, movement-related discharges that were comparable for cued and self-timed movements. On cued movements, neuronal activity increased sharply following cue onset. However, for self-timed movements, there was a slow build-up in activity that preceded the phasic discharge. This slow build-up was time-locked to movement and restricted to a narrow time window hundreds of milliseconds before movement. The difference in premovement activity between cued and self-timed trials was present before the earliest cue-onset times and was not related to any differences in the overall time-to-move between the two types of trials. These features suggest that activity evolving in the basal ganglia-cortical circuitry may drive the initiation of movements by increasing until an activity threshold is exceeded. The activity may increase abruptly in response to an external cue or gradually when the timing of movements is determined by the animals themselves rather than an external cue. In this view, small changes in activity that occur in advance of the much larger perimovement neuronal activity may be an important determinant of when movement occurs. In support of this hypothesis, we found that even for cued movements, faster reaction times were associated with slightly higher levels of activity hundreds of milliseconds before movement.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
M. A. Lebedev, J. E. O'Doherty, and M. A. L. Nicolelis
Decoding of Temporal Intervals From Cortical Ensemble Activity
J Neurophysiol, January 1, 2008; 99(1): 166 - 186.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Tanaka
Cognitive Signals in the Primate Motor Thalamus Predict Saccade Timing
J. Neurosci., October 31, 2007; 27(44): 12109 - 12118.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. H. Snyder, A. R. Dickinson, and J. L. Calton
Preparatory Delay Activity in the Monkey Parietal Reach Region Predicts Reach Reaction Times
J. Neurosci., October 4, 2006; 26(40): 10091 - 10099.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
I. H. Lee, A. R. Seitz, and J. A. Assad
Activity of Tonically Active Neurons in the Monkey Putamen During Initiation and Withholding of Movement
J Neurophysiol, April 1, 2006; 95(4): 2391 - 2403.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. Leblois, T. Boraud, W. Meissner, H. Bergman, and D. Hansel
Competition between feedback loops underlies normal and pathological dynamics in the basal ganglia.
J. Neurosci., March 29, 2006; 26(13): 3567 - 3583.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
G. Maimon and J. A. Assad
Parietal Area 5 and the Initiation of Self-Timed Movements versus Simple Reactions
J. Neurosci., March 1, 2006; 26(9): 2487 - 2498.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
K. R. Bailey and R. G. Mair
The Role of Striatum in Initiation and Execution of Learned Action Sequences in Rats
J. Neurosci., January 18, 2006; 26(3): 1016 - 1025.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. Amirnovin, Z. M. Williams, G. R. Cosgrove, and E. N. Eskandar
Visually Guided Movements Suppress Subthalamic Oscillations in Parkinson's Disease Patients
J. Neurosci., December 15, 2004; 24(50): 11302 - 11306.
[Abstract] [Full Text] [PDF]




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