Literature DB >> 8519334

The control of slow orienting eye movements by tectoreticulospinal neurons in the cat: behavior, discharge patterns and underlying connections.

E Olivier1, A Grantyn, M Chat, A Berthoz.   

Abstract

The activity of tectoreticulospinal neurons (TRSN) during orienting gaze shifts was studied in alert, head-fixed cats by intra-axonal recordings. The scope of the study was to evaluate the role of this class of superior colliculus neurons in the generation of slow eye movements (drifts) which often follow main-sequence saccades and sometimes appear as an independent motor event of orienting. The parameters of such movements are described in the first part of the paper. The organization of underlying pathways in the lower brainstem has been studied by intra-axonal horseradish peroxidase (HRP) tracing. The mean amplitude of postsaccadic drifts (PSD) is 1.21 degrees (SD 0.63), but it can eventually reach 6-8 degrees. PSDs have mean velocity of 14.9 degrees/s (SD 4.28) and mean duration of 104.2 ms (SD 50.8). These two parameters are positively correlated with PSD amplitude. The presence of PSDs is usually associated with an increased neck muscle activity on the side toward which the eyes move. The durations of these two motor events show a reliable positive correlation. PSDs appear to occur when gaze error persists after a saccade and a correction is attempted by means of a slow eye movement and a head turn. The durations of TRSN bursts are, on average, longer than the sum of the lead time and the saccade duration. Bursts associated with combinations of saccades and PSD are significantly longer than those recorded in the absence of PSDs. The probability of occurrence of PSDs is higher when firing of TRSNs continues after saccade termination. Such prolonged discharges usually coincide with a combination of PSDs and phasic activation of the neck electromyogram. The mean firing rate of TRSNs during PSDs is 62% of that during saccade-related portions of the burst and declines to 45% after the end of PSDs. According to its timing and intensity, postsaccadic firing of TRSNs is appropriate as a signal underlying slow, corrective eye movements and later portions of phasic neck muscle contractions during orienting. Intra-axonal HRP labeling showed that visuomotor TRSNs of the X type (n = 3) terminate in the abducens nucleus, with 145-331 boutons terminaux and en passant. Average bouton densities in the nucleus are lower than in the periabducens reticular formation, but higher than in more rostral paramedian pontine reticular formation (PPRF) regions. Terminal fields in the PPRF match the locations of "eye-neck' reticulospinal neurons (RSNs) and exitatory burst neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8519334     DOI: 10.1007/BF00229359

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  45 in total

1.  Overlapping saccades and glissades are produced by fatigue in the saccadic eye movement system.

Authors:  A T Bahill; L Stark
Journal:  Exp Neurol       Date:  1975-07       Impact factor: 5.330

2.  Characteristics of cat's eye saccades in different states of alertness.

Authors:  M Crommelinck; A Roucoux
Journal:  Brain Res       Date:  1976-02-27       Impact factor: 3.252

3.  Superior colliculus neurons mediate the dynamic characteristics of saccades.

Authors:  D M Waitzman; T P Ma; L M Optican; R H Wurtz
Journal:  J Neurophysiol       Date:  1991-11       Impact factor: 2.714

Review 4.  Signal transformations required for the generation of saccadic eye movements.

Authors:  D L Sparks; L E Mays
Journal:  Annu Rev Neurosci       Date:  1990       Impact factor: 12.449

5.  A parametric analysis of human saccades in different experimental paradigms.

Authors:  A C Smit; J A Van Gisbergen; A R Cools
Journal:  Vision Res       Date:  1987       Impact factor: 1.886

6.  Corrective movements following refixation saccades: type and control system analysis.

Authors:  R B Weber; R B Daroff
Journal:  Vision Res       Date:  1972-03       Impact factor: 1.886

7.  Burst activity of identified tecto-reticulo-spinal neurons in the alert cat.

Authors:  A Grantyn; A Berthoz
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

8.  Reticulovestibular organization participating in generation of horizontal fast eye movement.

Authors:  S Sasaki; H Shimazu
Journal:  Ann N Y Acad Sci       Date:  1981       Impact factor: 5.691

9.  Axonal patterns and sites of termination of cat superior colliculus neurons projecting in the tecto-bulbo-spinal tract.

Authors:  A Grantyn; R Grantyn
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

10.  Horizontal eye position-related activity in neck muscles of the alert cat.

Authors:  P P Vidal; A Roucoux; A Berthoz
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

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  11 in total

1.  Modeling LGN responses during free-viewing: a possible role of microscopic eye movements in the refinement of cortical orientation selectivity.

Authors:  M Rucci; G M Edelman; J Wray
Journal:  J Neurosci       Date:  2000-06-15       Impact factor: 6.167

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.  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

4.  Smooth eye movements evoked by electrical stimulation of the cat's superior colliculus.

Authors:  M Missal; P Lefèvre; A Delinte; M Crommelinck; A Roucoux
Journal:  Exp Brain Res       Date:  1996       Impact factor: 1.972

5.  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

6.  Combined eye-head gaze shifts to visual and auditory targets in humans.

Authors:  J E Goldring; M C Dorris; B D Corneil; P A Ballantyne; D P Munoz
Journal:  Exp Brain Res       Date:  1996-09       Impact factor: 1.972

7.  Post-spike facilitation of neck EMG by cat tectoreticulospinal neurones during orienting movements.

Authors:  E Olivier; A Grantyn; T Kitama; A Berthoz
Journal:  J Physiol       Date:  1995-01-15       Impact factor: 5.182

8.  Slow correcting eye movements of head-fixed, trained cats toward stationary targets.

Authors:  M Missal; M Crommelinck; A Roucoux; M F Decostre
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

9.  The fixation area of the cat superior colliculus: effects of electrical stimulation and direct connection with brainstem omnipause neurons.

Authors:  M Paré; D Guitton
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

10.  Gaze shifts evoked by stimulation of the superior colliculus in the head-free cat conform to the motor map but also depend on stimulus strength and fixation activity.

Authors:  M Paré; M Crommelinck; D Guitton
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

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