Literature DB >> 7897487

Use of interrupted saccade paradigm to study spatial and temporal dynamics of saccadic burst cells in superior colliculus in monkey.

E L Keller1, J A Edelman.   

Abstract

1. We recorded the spatial and temporal dynamics of saccade-related burst neurons (SRBNs) found in the intermediate layers of the superior colliculus (SC) in the alert, behaving monkey. These burst cells are normally the first neurons recorded during radially directed microelectrode penetrations of the SC after the electrode has left the more dorsally situated visual layers. They have spatially delimited movement fields whose centers describe the well-studied motor map of the SC. They have a rather sharp, saccade-locked burst of activity that peaks just before saccade onset and then declines steeply during the saccade. Many of these cells, when recorded during saccade trials, also have an early, transient visual response and an irregular prelude of presaccadic activity. 2. Because saccadic eye movements normally have very stereotyped durations and velocity trajectories that vary systematically with saccade size, it has been difficult in the past to establish quantitatively whether the activity of SRBNs temporally codes dynamic saccadic control signals, e.g., dynamic motor error or eye velocity, where dynamic motor error is defined as a signal proportional to the instantaneous difference between desired final eye position and the actual eye position during a saccade. It has also not been unequivocally established whether SRBNs participate in an organized spatial shift of ensemble activity in the intermediate layers of the SC during saccadic eye movements. 3. To address these issues, we studied the activity of SRBNs using an interrupted saccade paradigm. Saccades were interrupted with pulsatile electrical stimulation through a microelectrode implanted in the omnipauser region of the brain stem while recordings were made simultaneously from single SRBNs in the SC. 4. Shortly after the beginning of the stimulation (which was electronically triggered at saccade onset), the eyes decelerated rapidly and stopped completely. When the high-frequency (typically 300-400 pulses per second) stimulation was terminated (average duration 12 ms), the eye movement was reinitiated and a resumed saccade was made accurately to the location of the target. 5. When we recorded from SRBNs in the more caudal colliculus, which were active for large saccades, cell discharge was powerfully and rapidly suppressed by the stimulation (average latency = 3.8 ms). Activity in the same cells started again just before the onset of the resumed saccade and continued during this saccade even though it has a much smaller amplitude than would normally be associated with significant discharge for caudal SC cells.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7897487     DOI: 10.1152/jn.1994.72.6.2754

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


  25 in total

1.  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

2.  TMS perturbs saccade trajectories and unmasks an internal feedback controller for saccades.

Authors:  Minnan Xu-Wilson; Jing Tian; Reza Shadmehr; David S Zee
Journal:  J Neurosci       Date:  2011-08-10       Impact factor: 6.167

3.  Simulations of saccade curvature by models that place superior colliculus upstream from the local feedback loop.

Authors:  Mark M G Walton; David L Sparks; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2004-12-22       Impact factor: 2.714

4.  Spatial characteristics of neurons in the central mesencephalic reticular formation (cMRF) of head-unrestrained monkeys.

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

5.  Properties of saccades generated as a choice response.

Authors:  Kyoung-Min Lee; Edward L Keller; Stephen J Heinen
Journal:  Exp Brain Res       Date:  2004-12-10       Impact factor: 1.972

6.  Incomplete suppression of distractor-related activity in the frontal eye field results in curved saccades.

Authors:  Robert M McPeek
Journal:  J Neurophysiol       Date:  2006-08-02       Impact factor: 2.714

7.  Membrane channel properties of premotor excitatory burst neurons may underlie saccade slowing after lesions of omnipause neurons.

Authors:  Kenichiro Miura; Lance M Optican
Journal:  J Comput Neurosci       Date:  2006-02-20       Impact factor: 1.621

8.  Dissociation of eye and head components of gaze shifts by stimulation of the omnipause neuron region.

Authors:  Neeraj J Gandhi; David L Sparks
Journal:  J Neurophysiol       Date:  2007-05-09       Impact factor: 2.714

9.  Inhibition of voluntary saccadic eye movement commands by abrupt visual onsets.

Authors:  Jay A Edelman; Kitty Z Xu
Journal:  J Neurophysiol       Date:  2008-11-19       Impact factor: 2.714

10.  Changes in the response rate and response variability of area V4 neurons during the preparation of saccadic eye movements.

Authors:  Nicholas A Steinmetz; Tirin Moore
Journal:  J Neurophysiol       Date:  2009-12-16       Impact factor: 2.714

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