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


     


J Neurophysiol 53: 1401-1416, 1985;
0022-3077/85 $5.00
This Article
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 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 Google Scholar
Google Scholar
Right arrow Articles by Alexander, G. E.
Right arrow Articles by DeLong, M. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Alexander, G. E.
Right arrow Articles by DeLong, M. R.

Journal of Neurophysiology, Vol 53, Issue 6 1401-1416, Copyright © 1985 by APS


ARTICLES

Microstimulation of the primate neostriatum. I. Physiological properties of striatal microexcitable zones

G. E. Alexander and M. R. DeLong

Microstimulation was carried out at over 1,250 sites in the putamen in four unanesthetized rhesus monkeys. At numerous sites, microstimulation resulted in movements of individual body parts including leg, arm, and face. Microstimulation-evoked limb movements were invariably contralateral to the stimulating electrode. In nearly all instances, the response at threshold was restricted to or maximal about a single joint. A small percentage of stimulation-evoked axial and orofacial movements were bilateral. The same motor response was frequently evoked over distances of up to 1,200 micron along a single penetration, suggesting that a relatively homogeneous motor-response zone underlies the observed micro-stimulation effects. We have designated these presumptive functional units striatal microexcitable zones (SMZ). The boundaries of adjacent SMZ involved in different movements frequently appeared to overlap. Amplitude, velocity, and acceleration of microstimulation-evoked elbow movements were assessed quantitatively. With increasing stimulus current, each of these parameters increased monotonically until saturation occurred. The spread of intrastriatal microstimulation currents was found to be comparable to that reported for motor cortex. The effective radius of 40-microA putamen microstimulation currents was estimated to be approximately 150 micron. This effectively rules out the possibility of current spread to the internal capsule. Microstimulation effects were abolished by fiber-sparing lesions produced by microinjections of the neurotoxin ibotenic acid. Moreover, chronaxie measurements in putamen (327 +/- 47 microseconds) were significantly higher than for capsular stimulation (150 +/- 32 microseconds). These observations are consistent with the proposal that movements evoked by putamen microstimulation resulted from activation of putamen output neurons. On the other hand, a possible contribution from the antidromic activation of corticostriate afferent terminals or axons cannot be excluded.


This article has been cited by other articles:


Home page
J. Neurosci.Home page
M. Rivlin-Etzion, O. Marmor, G. Saban, B. Rosin, S. N. Haber, E. Vaadia, Y. Prut, and H. Bergman
Low-Pass Filter Properties of Basal Ganglia Cortical Muscle Loops in the Normal and MPTP Primate Model of Parkinsonism
J. Neurosci., January 16, 2008; 28(3): 633 - 649.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. D. Humphries, R. D. Stewart, and K. N. Gurney
A Physiologically Plausible Model of Action Selection and Oscillatory Activity in the Basal Ganglia
J. Neurosci., December 13, 2006; 26(50): 12921 - 12942.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
M. Rodriguez, I. Morales, I. Gomez, S. Gonzalez, T. Gonzalez-Hernandez, and J. L. Gonzalez-Mora
Heterogeneous Dopamine Neurochemistry in the Striatum: The Fountain-Drain Matrix
J. Pharmacol. Exp. Ther., October 1, 2006; 319(1): 31 - 43.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. Courtemanche, N. Fujii, and A. M. Graybiel
Synchronous, Focally Modulated {beta}-Band Oscillations Characterize Local Field Potential Activity in the Striatum of Awake Behaving Monkeys
J. Neurosci., December 17, 2003; 23(37): 11741 - 11752.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Nambu, K. Kaneda, H. Tokuno, and M. Takada
Organization of Corticostriatal Motor Inputs in Monkey Putamen
J Neurophysiol, October 1, 2002; 88(4): 1830 - 1842.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
L. Maillard, K. Ishii, K. Bushara, D. Waldvogel, A. E. Schulman, and M. Hallett
Mapping the basal ganglia: fMRI evidence for somatotopic representation of face, hand, and foot
Neurology, August 8, 2000; 55(3): 377 - 383.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
A. L. Kendall, F. David, G. Rayment, E. M. Torres, L. E. Annett, and S. B. Dunnett
The influence of excitotoxic basal ganglia lesions on motor performance in the common marmoset
Brain, July 1, 2000; 123(7): 1442 - 1458.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
N. Matsumoto, T. Hanakawa, S. Maki, A. M. Graybiel, and M. Kimura
Nigrostriatal Dopamine System in Learning to Perform Sequential Motor Tasks in a Predictive Manner
J Neurophysiol, August 1, 1999; 82(2): 978 - 998.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. E. Kincaid, T. Zheng, and C. J. Wilson
Connectivity and Convergence of Single Corticostriatal Axons
J. Neurosci., June 15, 1998; 18(12): 4722 - 4731.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Merchant, A. Zainos, A. Hernandez, E. Salinas, and R. Romo
Functional Properties of Primate Putamen Neurons During the Categorization of Tactile Stimuli
J Neurophysiol, March 1, 1997; 77(3): 1132 - 1154.
[Abstract] [Full Text] [PDF]




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