Literature DB >> 12686582

Smooth-pursuit eye-movement-related neuronal activity in macaque nucleus reticularis tegmenti pontis.

David A Suzuki1, Tetsuto Yamada, Robert D Yee.   

Abstract

Neuronal responses that were observed during smooth-pursuit eye movements were recorded from cells in rostral portions of the nucleus reticularis tegmenti pontis (rNRTP). The responses were categorized as smooth-pursuit eye velocity (78%) or eye acceleration (22%). A separate population of rNRTP cells encoded static eye position. The sensitivity to pursuit eye velocity averaged 0.81 spikes/s per degrees /s, whereas the average sensitivity to pursuit eye acceleration was 0.20 spikes/s per degrees /s(2). Of the eye-velocity cells with horizontal preferences for pursuit responses, 56% were optimally responsive to contraversive smooth-pursuit eye movements and 44% preferred ipsiversive pursuit. For cells with vertical pursuit preferences, 61% preferred upward pursuit and 39% preferred downward pursuit. The direction selectivity was broad with 50% of the maximal response amplitude observed for directions of smooth pursuit up to +/-85 degrees away from the optimal direction. The activities of some rNRTP cells were linearly related to eye position with an average sensitivity of 2.1 spikes/s per deg. In some cells, the magnitude of the response during smooth-pursuit eye movements was affected by the position of the eyes even though these cells did not encode eye position. On average, pursuit centered to one side of screen center elicited a response that was 73% of the response amplitude obtained with tracking centered at screen center. For pursuit centered on the opposite side, the average response was 127% of the response obtained at screen center. The results provide a neuronal rationale for the slow, pursuit-like eye movements evoked with rNRTP microstimulation and for the deficits in smooth-pursuit eye movements observed with ibotenic acid injection into rNRTP. More globally, the results support the notion of a frontal and supplementary eye field-rNRTP-cerebellum pathway involved with controlling smooth-pursuit eye movements.

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Year:  2003        PMID: 12686582     DOI: 10.1152/jn.00117.2002

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


  14 in total

1.  Visual error signals from the pretectal nucleus of the optic tract guide motor learning for smooth pursuit.

Authors:  Seiji Ono; Michael J Mustari
Journal:  J Neurophysiol       Date:  2010-05       Impact factor: 2.714

2.  Specific vermal complex spike responses build up during the course of smooth-pursuit adaptation, paralleling the decrease of performance error.

Authors:  Suryadeep Dash; Nicolas Catz; Peter Wilhelm Dicke; Peter Thier
Journal:  Exp Brain Res       Date:  2010-06-24       Impact factor: 1.972

3.  A model that integrates eye velocity commands to keep track of smooth eye displacements.

Authors:  Gunnar Blohm; Lance M Optican; Philippe Lefèvre
Journal:  J Comput Neurosci       Date:  2006-04-22       Impact factor: 1.621

4.  Gaze pursuit responses in nucleus reticularis tegmenti pontis of head-unrestrained macaques.

Authors:  David A Suzuki; Kathleen F Betelak; Robert D Yee
Journal:  J Neurophysiol       Date:  2008-11-05       Impact factor: 2.714

5.  A theory of the dual pathways for smooth pursuit based on dynamic gain control.

Authors:  Ulrich Nuding; Seiji Ono; Michael J Mustari; Ulrich Büttner; Stefan Glasauer
Journal:  J Neurophysiol       Date:  2008-04-02       Impact factor: 2.714

6.  The response of MSTd neurons to perturbations in target motion during ongoing smooth-pursuit eye movements.

Authors:  Seiji Ono; Lukas Brostek; Ulrich Nuding; Stefan Glasauer; Ulrich Büttner; Michael J Mustari
Journal:  J Neurophysiol       Date:  2009-11-18       Impact factor: 2.714

7.  A mechanism for decision rule discrimination by supplementary eye field neurons.

Authors:  Supriya Ray; Stephen J Heinen
Journal:  Exp Brain Res       Date:  2014-11-05       Impact factor: 1.972

8.  Short-term saccadic adaptation in the macaque monkey: a binocular mechanism.

Authors:  K P Schultz; C Busettini
Journal:  J Neurophysiol       Date:  2012-10-17       Impact factor: 2.714

9.  Learning the trajectory of a moving visual target and evolution of its tracking in the monkey.

Authors:  Clara Bourrelly; Julie Quinet; Patrick Cavanagh; Laurent Goffart
Journal:  J Neurophysiol       Date:  2016-09-28       Impact factor: 2.714

10.  Lesions of the cerebellar nodulus and uvula impair downward pursuit.

Authors:  Mark F Walker; Jing Tian; Xiaoyan Shan; Rafael J Tamargo; Howard Ying; David S Zee
Journal:  J Neurophysiol       Date:  2008-07-23       Impact factor: 2.714

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