JN Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 75: 1546-1572, 1996;
0022-3077/96 $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 Waitzman, D. M.
Right arrow Articles by Cohen, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Waitzman, D. M.
Right arrow Articles by Cohen, B.

Journal of Neurophysiology, Vol 75, Issue 4 1546-1572, Copyright © 1996 by APS


ARTICLES

Central mesencephalic reticular formation (cMRF) neurons discharging before and during eye movements

D. M. Waitzman, V. L. Silakov and B. Cohen
Department of Neurology, VA Connecticut Healthcare System, Newington, USA.

1. One hundred twenty neurons were recorded in the central mesencephalic reticular formation (cMRF) of four rhesus monkeys, trained to make visually guided and targeted saccadic eye movements. Eye movements were recorded with the head fixed, using electrooculography (EOG) or subconjunctival scleral search coils. Seventy-six percent (92/120) of cells discharged before and during contraversive visually guided or targeted rapid eye movements, and 76% of these (70/92) responded during contraversive spontaneous saccades in the dark. cMRF neurons had large contraversive movement fields and either a high (> 10 spikes/s) or low background level of spontaneous activity in the dark. The optimal movement vectors (i.e., saccades with greatest response) were predominantly horizontal, although many had a vertical component. Cells with optimal movement vectors within +/- 25 degrees of pure vertical were more rostral in the MRF and were excluded from the analysis. 2. A subgroup of cMRF neurons (31 of 92) that discharged before and during visually guided saccades were examined for visual sensitivity. Slightly less than one-half of these cells (42%, 13/31) were visuomotor units, i.e., they responded to visual targets in the absence of eye movement. The other 58% (n = 18) did not discharge during the visual probe trial; they were movement-related cells. 3. Microstimulation (threshold 40-60 microA at 333 Hz) at the sites of many of these cMRF neurons produced contraversive saccadic eye movements at short latency (< 40 ms). The amplitude and direction of the elicited saccades were similar to the optimal movement vector determined from single-unit recording. This suggested that cMRF cells recorded at the same locus of electrical microstimulation participated in the network responsible for the production and control of rapid eye movements. 4. The 92 saccade-related neurons were divided into two groups on the basis of their background discharge rate. Firing rates for both low background (28%, n = 26) and high background (72%, n = 66) cells increased approximately 30 ms before contraversive saccades and reached a peak discharge just before saccade onset. The low background neurons had either no activity or generated a few spikes just before the end of ipsiversive saccades. The steady rate of discharge (> 10 spikes/s) of high background neurons was inhibited from approximately 20 ms before ipsiversive saccades until just before saccade end. 5. Cells were also subdivided on the basis of how their discharge rates fell at the end of saccades. Clipped cells (38%, n = 35) had activity that fell sharply with saccade offset. Partially clipped cells (62%, n = 57) had persistent firing in the 100 ms following the saccade that was > 20% higher than the firing during the 100 ms before the saccade. 6. Latencies between the 90% point on the rising edge of the peak discharge and the start of the saccade were < or = 5.3 ms for eye movement-related cells in two monkeys. Longer latencies (11-19 ms) were found when measured between the 10% point on the rising edge of the peak discharge and saccade onset. These latencies were equal to or shorter than those obtained for eye movement-related burst neurons in the intermediate and deep layers of the superior colliculus analyzed similarly. Delays between the peak discharge and peak eye velocity were 13.6-15.1 ms for the same group of cMRF eye movement-related cells. These were significantly shorter than the delays measured for eye movement neurons in the superior colliculus (SC) of one of the monkeys. These findings suggest that the buildup discharge of cMRF neurons occurs early enough before saccades to contribute to saccade triggering. The peak discharge, however, occurs with or after the burst in the SC, suggesting that this portion of the discharge serves a function other than saccade triggering. 7. The number of spikes in bursts associated with eye movement was correlated with saccade parameters.


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
J. A. Cromer and D. M. Waitzman
Comparison of Saccade-Associated Neuronal Activity in the Primate Central Mesencephalic and Paramedian Pontine Reticular Formations
J Neurophysiol, August 1, 2007; 98(2): 835 - 850.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
S. Ramat, R. J. Leigh, D. S. Zee, and L. M. Optican
What clinical disorders tell us about the neural control of saccadic eye movements
Brain, January 1, 2007; 130(1): 10 - 35.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
J. A. Cromer and D. M. Waitzman
Neurones associated with saccade metrics in the monkey central mesencephalic reticular formation
J. Physiol., February 1, 2006; 570(3): 507 - 523.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
T. Rezaie, D. M. Waitzman, J. L. Seeman, P. L. Kaufman, and M. Sarfarazi
Molecular Cloning and Expression Profiling of Optineurin in the Rhesus Monkey
Invest. Ophthalmol. Vis. Sci., July 1, 2005; 46(7): 2404 - 2410.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. M. G. Walton, D. L. Sparks, and N. J. Gandhi
Simulations of Saccade Curvature by Models That Place Superior Colliculus Upstream From the Local Feedback Loop
J Neurophysiol, April 1, 2005; 93(4): 2354 - 2358.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. D. Crawford, D. B. Tweed, and T. Vilis
Static Ocular Counterroll Is Implemented Through the 3-D Neural Integrator
J Neurophysiol, October 1, 2003; 90(4): 2777 - 2784.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. M. Klier, H. Wang, and J. D. Crawford
Three-Dimensional Eye-Head Coordination Is Implemented Downstream From the Superior Colliculus
J Neurophysiol, May 1, 2003; 89(5): 2839 - 2853.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. Soetedjo, C. R. S. Kaneko, and A. F. Fuchs
Evidence That the Superior Colliculus Participates in the Feedback Control of Saccadic Eye Movements
J Neurophysiol, February 1, 2002; 87(2): 679 - 695.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. M. Waitzman, V. L. Silakov, S. DePalma-Bowles, and A. S. Ayers
Effects of Reversible Inactivation of the Primate Mesencephalic Reticular Formation. I. Hypermetric Goal-Directed Saccades
J Neurophysiol, April 1, 2000; 83(4): 2260 - 2284.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. M. Waitzman, V. L. Silakov, S. DePalma-Bowles, and A. S. Ayers
Effects of Reversible Inactivation of the Primate Mesencephalic Reticular Formation. II. Hypometric Vertical Saccades
J Neurophysiol, April 1, 2000; 83(4): 2285 - 2299.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Takagi, D. S. Zee, and R. J. Tamargo
Effects of Lesions of the Oculomotor Vermis on Eye Movements in Primate: Saccades
J Neurophysiol, October 1, 1998; 80(4): 1911 - 1931.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. R. S. Kaneko and K. Fukushima
Discharge Characteristics of Vestibular Saccade Neurons in Alert Monkeys
J Neurophysiol, February 1, 1998; 79(2): 835 - 847.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Handel and P. W. Glimcher
Response Properties of Saccade-Related Burst Neurons in the Central Mesencephalic Reticular Formation
J Neurophysiol, October 1, 1997; 78(4): 2164 - 2175.
[Abstract] [Full Text] [PDF]




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