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


     


J Neurophysiol 66: 1605-1623, 1991;
0022-3077/91 $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 Guitton, D.
Right arrow Articles by Munoz, D. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Guitton, D.
Right arrow Articles by Munoz, D. P.

Journal of Neurophysiology, Vol 66, Issue 5 1605-1623, Copyright © 1991 by APS


ARTICLES

Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. I. Identification, localization, and effects of behavior on sensory responses

D. Guitton and D. P. Munoz
Montreal Neurological Institute, Quebec, Canada.

1. The input-output connectivity, in cat, of tectoreticular (TRNs) and tectoreticulospinal (TRSNs) neurons [together called TR(S)Ns] suggests a role for these cells in the sensorimotor transformations necessary for controlling orienting behavior. Multimodal sensory information converges directly onto these tectal neurons, and they project to several brain stem and spinal cord centers involved in the control of eye- and head-orienting movements. In this and the following two papers, we describe the sensorimotor discharges of antidromically identified TR(S)Ns. Here we describe the process of localizing and identifying them, characteristics of both their antidromic and sensory responses, and effects of behavioral context on these responses. 2. In 13 alert, chronically prepared cats, a total of 293 neurons were antidromically identified from either the predorsal bundle (PDB) immediately rostral to abducens nucleus or the ventromedial funiculus of the spinal cord at the level of the first cervical vertebra (C1). The cell bodies of all identified TR(S)Ns were confined to the intermediate and deep laminae of the superior colliculus (SC). The antidromic nature of the action potential evoked by stimulating either the PDB or C1 was verified by the use of a number of established criteria, including collision testing. 3. The mean antidromic latency from the PDB (TRNs + TRSNs) was 0.84 +/- 0.59 (SD) ms (n = 217). The conduction velocities of all cells activated by PDB stimulation ranged from 4 to 40 m/s. The mean latency from C1 (TRSNs) was 1.03 +/- 0.52 ms (SD) (n = 64), whereas conduction velocities ranged from 14 to 80 m/s. 4. One hundred thirty-eight TR(S)Ns were studied long enough to yield significant data regarding their involvement in visuomotor-orienting behavior. Ninety-eight percent (130/133) of the TR(S)Ns tested for visual responses could be induced to discharge action potentials in response to some form of visual stimulation. The other three neurons remained silent, even in response to the most provocative stimuli. These silent neurons nevertheless were shown to be depolarized by visual stimuli. TR(S)Ns were occasionally tested for auditory and somatosensory responses and some were multimodal. 5. TR(S)Ns had visual receptive fields that conformed to the retinotopic map of the visual field that is represented within the SC. Cells found in the lateral SC had receptive fields located in the lower visual field, whereas neurons that were situated medially had receptive fields in the upper visual field. Cells found in the rostral SC had small fields that included a representation of the area centralis.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
R. A. Marino, C. K. Rodgers, R. Levy, and D. P. Munoz
Spatial Relationships of Visuomotor Transformations in the Superior Colliculus Map
J Neurophysiol, November 1, 2008; 100(5): 2564 - 2576.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. R. Sinha and C. F. Moss
Vocal Premotor Activity in the Superior Colliculus
J. Neurosci., January 3, 2007; 27(1): 98 - 110.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. E. Cullen, M. Huterer, D. A. Braidwood, and P. A. Sylvestre
Time Course of Vestibuloocular Reflex Suppression During Gaze Shifts
J Neurophysiol, December 1, 2004; 92(6): 3408 - 3422.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. P. Doubell, I. Skaliora, J. Baron, and A. J. King
Functional Connectivity between the Superficial and Deeper Layers of the Superior Colliculus: An Anatomical Substrate for Sensorimotor Integration
J. Neurosci., July 23, 2003; 23(16): 6596 - 6607.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
Y. Saito and T. Isa
Local Excitatory Network and NMDA Receptor Activation Generate a Synchronous and Bursting Command from the Superior Colliculus
J. Neurosci., July 2, 2003; 23(13): 5854 - 5864.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Bergeron and D. Guitton
In Multiple-Step Gaze Shifts: Omnipause (OPNs) and Collicular Fixation Neurons Encode Gaze Position Error; OPNs Gate Saccades
J Neurophysiol, October 1, 2002; 88(4): 1726 - 1742.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. L. Keller, R. M. McPeek, and T. Salz
Evidence Against Direct Connections to PPRF EBNs From SC in the Monkey
J Neurophysiol, September 1, 2000; 84(3): 1303 - 1313.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
Y. Izawa, Y. Sugiuchi, and Y. Shinoda
Neural Organization From the Superior Colliculus to Motoneurons in the Horizontal Oculomotor System of the Cat
J Neurophysiol, June 1, 1999; 81(6): 2597 - 2611.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. T. Wallace, M. A. Meredith, and B. E. Stein
Multisensory Integration in the Superior Colliculus of the Alert Cat
J Neurophysiol, August 1, 1998; 80(2): 1006 - 1010.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Pare and D. Guitton
Brain Stem Omnipause Neurons and the Control of CombinedEye-Head Gaze Saccades in the Alert Cat
J Neurophysiol, June 1, 1998; 79(6): 3060 - 3076.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. E. Cullen and D. Guitton
Analysis of Primate IBN Spike Trains Using System Identification Techniques. III. Relationship to Motor Error During Head-Fixed Saccades and Head-Free Gaze Shifts
J Neurophysiol, December 1, 1997; 78(6): 3307 - 3322.
[Abstract] [Full Text] [PDF]




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