Literature DB >> 1765799

Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. III. Spatiotemporal characteristics of phasic motor discharges.

D P Munoz1, D Guitton, D Pélisson.   

Abstract

1. In this paper we describe the movement-related discharges of tectoreticular and tectoreticulospinal neurons [together called TR (S) Ns] that were recorded in the superior colliculus (SC) of alert cats trained to generate orienting movements in various behavioral situations; the cats' heads were either completely unrestrained (head free) or immobilized (head fixed). TR (S) Ns are organized into a retinotopically coded motor map. These cells can be divided into two groups, fixation TR (S) Ns [f TR (S) Ns] and orientation TR (S) Ns [oTR(S)Ns], depending on whether they are located, respectively, within or outside the zero (or area centralis) representation of the motor map in the rostral SC. 2. oTR(S)Ns discharged phasic motor bursts immediately before the onset of gaze shifts in both the head-free and head-fixed conditions. Ninety-five percent of the oTR(S)Ns tested (62/65) increased their rate of discharge before a visually triggered gaze shift, the amplitude and direction of which matched the cell's preferred movement vector. For movements along the optimal direction, each cell produced a burst discharge for gaze shifts of all amplitudes equal to or greater than the optimum. Hence, oTR(S)Ns had no distal limit to their movement fields. The timing of the burst relative to the onset of the gaze shift, however, depended on gaze shift amplitude: each TR(S)N reached its peak discharge when the instantaneous position of the visual axis relative to the target (i.e., instantaneous gaze motor error) matched the cell's optimal vector, regardless of the overall amplitude of the movement. 3. The intensity of the movement-related burst discharge depended on the behavioral context. For the same vector, the movement-related increase in firing was greatest for visually triggered movements and less pronounced when the cat oriented to a predicted target, a condition in which only 76% of the cells tested (35/46) increased their discharge rate. The weakest movement-related discharges were associated with spontaneous gaze shifts. 4. For some oTR(S)Ns, the average firing frequency in the movement-related burst was correlated to the peak velocity of the movement trajectory in both head-fixed and head-free conditions. Typically, when the head was unrestrained, the correlation to peak gaze velocity was better than that to either peak eye or head velocity alone. 5. Gaze shifts triggered by a high-frequency train of collicular microstimulation had greater peak velocities than comparable amplitude movements elicited by a low-frequency train of stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1765799     DOI: 10.1152/jn.1991.66.5.1642

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


  47 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.  Kinematics and eye-head coordination of gaze shifts evoked from different sites in the superior colliculus of the cat.

Authors:  Alain Guillaume; Denis Pélisson
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

3.  Eye position modulates the electromyographic responses of neck muscles to electrical stimulation of the superior colliculus in the alert cat.

Authors:  K Hadjidimitrakis; A K Moschovakis; Y Dalezios; A Grantyn
Journal:  Exp Brain Res       Date:  2006-11-08       Impact factor: 1.972

4.  Role of the primate superior colliculus in the control of head movements.

Authors:  Mark M G Walton; Bernard Bechara; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2007-06-20       Impact factor: 2.714

5.  Effect of reversible inactivation of superior colliculus on head movements.

Authors:  Mark M G Walton; Bernard Bechara; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2008-02-27       Impact factor: 2.714

6.  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

7.  The feedback circuit connecting the central mesencephalic reticular formation and the superior colliculus in the macaque monkey: tectal connections.

Authors:  Lan Zhou; Susan Warren; Paul J May
Journal:  Exp Brain Res       Date:  2008-06-14       Impact factor: 1.972

8.  Coordination of eye and head components of movements evoked by stimulation of the paramedian pontine reticular formation.

Authors:  Neeraj J Gandhi; Ellen J Barton; David L Sparks
Journal:  Exp Brain Res       Date:  2008-05-06       Impact factor: 1.972

9.  A bilateral model integrating vergence and the vestibulo-ocular reflex.

Authors:  A C Cova; H L Galiana
Journal:  Exp Brain Res       Date:  1996       Impact factor: 1.972

10.  An anatomical substrate for the spatiotemporal transformation.

Authors:  A K Moschovakis; T Kitama; Y Dalezios; J Petit; A M Brandi; A A Grantyn
Journal:  J Neurosci       Date:  1998-12-01       Impact factor: 6.167

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