Literature DB >> 10085355

Action of the brain stem saccade generator during horizontal gaze shifts. I. Discharge patterns of omnidirectional pause neurons.

J O Phillips1, L Ling, A F Fuchs.   

Abstract

Omnidirectional pause neurons (OPNs) pause for the duration of a saccade in all directions because they are part of the neural mechanism that controls saccade duration. In the natural situation, however, large saccades are accompanied by head movements to produce rapid gaze shifts. To determine whether OPNs are part of the mechanism that controls the whole gaze shift rather than the eye saccade alone, we monitored the activity of 44 OPNs that paused for rightward and leftward gaze shifts but otherwise discharged at relatively constant average rates. Pause duration was well correlated with the duration of either eye or gaze movement but poorly correlated with the duration of head movement. The time of pause onset was aligned tightly with the onset of either eye or gaze movement but only loosely aligned with the onset of head movement. These data suggest that the OPN pause does not encode the duration of head movement. Further, the end of the OPN pause was often better aligned with the end of the eye movement than with the end of the gaze movement for individual gaze shifts. For most gaze shifts, the eye component ended with an immediate counterrotation owing to the vestibuloocular reflex (VOR), and gaze ended at variable times thereafter. In those gaze shifts where eye counterrotation was delayed, the end of the pause also was delayed. Taken together, these data suggest that the end of the pause influences the onset of eye counterrotation, not the end of the gaze shift. We suggest that OPN neurons act to control only that portion of the gaze movement that is commanded by the eye burst generator. This command is expressed by driving the saccadic eye movement directly and also by suppressing VOR eye counterrotation. Because gaze end is less well correlated with pause end and often occurs well after counterrotation onset, we conclude that elements of the burst generator typically are not active till gaze end, and that gaze end is determined by another mechanism independent of the OPNs.

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Year:  1999        PMID: 10085355     DOI: 10.1152/jn.1999.81.3.1284

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


  7 in total

1.  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

2.  Gaze displacement and inter-segmental coordination during large whole body voluntary rotations.

Authors:  Dimitri Anastasopoulos; Nausica Ziavra; Mark Hollands; Adolfo Bronstein
Journal:  Exp Brain Res       Date:  2008-11-12       Impact factor: 1.972

3.  Target modality determines eye-head coordination in nonhuman primates: implications for gaze control.

Authors:  Luis C Populin; Abigail Z Rajala
Journal:  J Neurophysiol       Date:  2011-07-27       Impact factor: 2.714

4.  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

5.  Spatial updating depends on gaze direction even after loss of vision.

Authors:  Johanna Reuschel; Frank Rösler; Denise Y P Henriques; Katja Fiehler
Journal:  J Neurosci       Date:  2012-02-15       Impact factor: 6.167

6.  Contribution of the frontal eye field to gaze shifts in the head-unrestrained rhesus monkey: neuronal activity.

Authors:  T A Knight
Journal:  Neuroscience       Date:  2012-09-01       Impact factor: 3.590

7.  Visual fixation as equilibrium: evidence from superior colliculus inactivation.

Authors:  Laurent Goffart; Ziad M Hafed; Richard J Krauzlis
Journal:  J Neurosci       Date:  2012-08-01       Impact factor: 6.167

  7 in total

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