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


     


J Neurophysiol 74: 73-95, 1995;
0022-3077/95 $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 Isa, T.
Right arrow Articles by Naito, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Isa, T.
Right arrow Articles by Naito, K.

Journal of Neurophysiology, Vol 74, Issue 1 73-95, Copyright © 1995 by APS


ARTICLES

Activity of neurons in the medial pontomedullary reticular formation during orienting movements in alert head-free cats

T. Isa and K. Naito
Department of Neurophysiology, Faculty of Medicine, University of Tokyo, Japan.

1. Single unit activities of 236 neurons were recorded in the medial pontomedullary reticular formation during visually triggered orienting gaze shifts in 10 alert cats under head-free conditions using movable tungsten-needle electrodes attached to the skull. The activities were analyzed mainly in relation to the head movement that was triggered by presentation of a light-emitting diode (LED) in one of eight directions separated radially by 45 deg after fixation of the center LED. Of these, 120 neurons were recorded in the pontine reticular formation, chiefly in the nucleus reticularis pontis caudalis, and the remaining 116 were in the medullary reticular formation, chiefly in the nucleus reticularis gigantocellularis. Activities of 65 pontine and 65 medullary neurons were modulated in relation to the dynamic phase of orienting movements ("orienting-related neurons"). Activities of the remaining neurons were modulated either irregularly or not at all during orienting movement ("irregular or no-response neurons"). Input from the contralateral superior colliculus and cerebral cortex and projections to the spinal cord were also investigated. 2. Among the orienting-related neurons, 62 pontine and 55 medullary neurons showed increases in activity preceding the onset of eye and head movement by 0-155 ms ("pretype"). Three pontine and 10 medullary neurons showed increases in activity only after the onset of movement ("posttype"). Of the pretype neurons, 61 pontine and 51 medullary neurons showed directional preference of activity ("directional" neurons). One pontine and four medullary neurons were classified as "omnidirectional" because these neurons increased activity preceding movements in all directions tested, and no directional preference was apparent. 3. In the pretype-directional cells, the average firing frequency during bursts was correlated with amplitude and angular velocity of head movements. Activities of the directional neurons during movements in the eight different directions could be well fitted with cosine functions in the majority of cases. The preferred directions of most pontine neurons and of about half the medullary neurons, as determined by first-degree sinusoidal regression analysis, were distributed around the ipsiversive horizontal axis. However, there were also a considerable number of neurons whose preferred directions were upward, downward, contraversive, or oblique in the medulla. 4. Among the directional cells preferring ipsiversive horizontal movements, 11 pontine neurons showed activity, the onset of which was locked to visual stimuli with latencies of 40-70 ms, in addition to phasic discharges locked to the onset of movement. This "stimulus-locked activity" was sometimes modulated depending on the attentional state of the animal.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
N. J. Gandhi and D. L. Sparks
Dissociation of Eye and Head Components of Gaze Shifts by Stimulation of the Omnipause Neuron Region
J Neurophysiol, July 1, 2007; 98(1): 360 - 373.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. D. Corneil, E. Olivier, and D. P. Munoz
Neck Muscle Responses to Stimulation of Monkey Superior Colliculus. I. Topography and Manipulation of Stimulation Parameters
J Neurophysiol, October 1, 2002; 88(4): 1980 - 1999.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. D. Corneil, E. Olivier, and D. P. Munoz
Neck Muscle Responses to Stimulation of Monkey Superior Colliculus. II. Gaze Shift Initiation and Volitional Head Movements
J Neurophysiol, October 1, 2002; 88(4): 2000 - 2018.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. D. Corneil, E. Olivier, F. J. R. Richmond, G. E. Loeb, and D. P. Munoz
Neck Muscles in the Rhesus Monkey. II. Electromyographic Patterns of Activation Underlying Postures and Movements
J Neurophysiol, October 1, 2001; 86(4): 1729 - 1749.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. K. Moschovakis, T. Kitama, Y. Dalezios, J. Petit, A. M. Brandi, and A. A. Grantyn
An Anatomical Substrate for the Spatiotemporal Transformation
J. Neurosci., December 1, 1998; 18(23): 10219 - 10229.
[Abstract] [Full Text] [PDF]




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