Literature DB >> 12037180

Evidence against a moving hill in the superior colliculus during saccadic eye movements in the monkey.

Robijanto Soetedjo1, Chris R S Kaneko, Albert F Fuchs.   

Abstract

Saccadic eye movements of different sizes and directions are represented in an orderly topographic map across the intermediate and deep layers of the superior colliculus (SC), where large saccades are encoded caudally and small saccades rostrally. Based on experiments in the cat, it has been suggested that saccades are initiated by a hill of activity at the caudal site appropriate for a particular saccade. As the saccade evolves and the remaining distance to the target, the motor error, decreases, the hill moves rostrally across successive SC sites responsible for saccades of increasingly smaller amplitudes. When the hill reaches the "fixation zone" in the rostral SC, the saccade is terminated. A moving hill of activity has also been posited for the monkey, in which it is supposed to be transported via so-called build-up neurons (BUNs), which have a prelude of activity that culminates in a burst for saccades. However, several studies using a variety of approaches have yet to provide conclusive evidence for or against a moving hill. The moving hill scenario predicts that during a large saccade the burst of a BUN in the rostral SC will be delayed until the motor error remaining in the evolving saccade is equal to the saccadic amplitude for which that BUN discharges best, i.e., its optimal amplitude. Therefore a plot of the burst lead preceding the "optimal" motor error against the time of occurrence of the optimal motor error should have a slope of zero. A slope of -1 indicates no moving hill. For our 20 BUNs, we used three measures of burst timing: the leads to the onset, peak, and center of the burst. The average slopes of these relations were -1.09, -0.79, and -0.58, respectively. For individual BUNs, the slopes of all three relations always differed significantly from zero. Although the peak and center leads fall between -1 and 0, a hill of activity moving rostrally at a rate indicated by either of these slopes would arrive at the fixation zone much too late to terminate the saccade at the appropriate time. Calculating our same three timing measures from averaged data leads us to the same conclusion. Thus our data do not support the moving hill model. However, we argue in the DISCUSSION that the constant lead of the burst onset relative to saccade onset (approximately 27 ms) suggests that the BUNs may help to trigger the saccade.

Mesh:

Year:  2002        PMID: 12037180     DOI: 10.1152/jn.2002.87.6.2778

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  16 in total

1.  Distractor modulation of saccade trajectories: spatial separation and symmetry effects.

Authors:  Eugene McSorley; Patrick Haggard; Robin Walker
Journal:  Exp Brain Res       Date:  2004-01-15       Impact factor: 1.972

2.  Evidence for gaze feedback to the cat superior colliculus: discharges reflect gaze trajectory perturbations.

Authors:  Satoshi Matsuo; André Bergeron; Daniel Guitton
Journal:  J Neurosci       Date:  2004-03-17       Impact factor: 6.167

3.  Behavior of the oculomotor vermis for five different types of saccade.

Authors:  Yoshiko Kojima; Robijanto Soetedjo; Albert F Fuchs
Journal:  J Neurophysiol       Date:  2010-10-20       Impact factor: 2.714

4.  Discharge of monkey nucleus reticularis tegmenti pontis neurons changes during saccade adaptation.

Authors:  N Takeichi; C R S Kaneko; A F Fuchs
Journal:  J Neurophysiol       Date:  2005-05-25       Impact factor: 2.714

5.  Saccade-related, long-lead burst neurons in the monkey rostral pons.

Authors:  Chris R S Kaneko
Journal:  J Neurophysiol       Date:  2005-10-19       Impact factor: 2.714

6.  The effects of a task-irrelevant visual event on spatial working memory.

Authors:  Stefan Van der Stigchel; Hannke Merten; Martun Meeter; Jan Theeuwes
Journal:  Psychon Bull Rev       Date:  2007-12

7.  Temporal characteristics of neurons in the central mesencephalic reticular formation of head unrestrained monkeys.

Authors:  Jay S Pathmanathan; Jason A Cromer; Kathleen E Cullen; David M Waitzman
Journal:  Exp Brain Res       Date:  2005-11-15       Impact factor: 1.972

8.  Modeling eye-head gaze shifts in multiple contexts without motor planning.

Authors:  Iman Haji-Abolhassani; Daniel Guitton; Henrietta L Galiana
Journal:  J Neurophysiol       Date:  2016-07-20       Impact factor: 2.714

9.  Changes in simple spike activity of some Purkinje cells in the oculomotor vermis during saccade adaptation are appropriate to participate in motor learning.

Authors:  Yoshiko Kojima; Robijanto Soetedjo; Albert F Fuchs
Journal:  J Neurosci       Date:  2010-03-10       Impact factor: 6.167

10.  Firing patterns in superior colliculus of head-unrestrained monkey during normal and perturbed gaze saccades reveal short-latency feedback and a sluggish rostral shift in activity.

Authors:  Woo Young Choi; Daniel Guitton
Journal:  J Neurosci       Date:  2009-06-03       Impact factor: 6.167

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