Literature DB >> 11960798

Contribution of the superior colliculus and the mesencephalic reticular formation to gaze control.

David M Waitzman1, Jay Pathmanathan, Rachel Presnell, Amanda Ayers, Stacy DePalma.   

Abstract

Converging lines of evidence support a role for the intermediate and deep layers of the superior colliculus (SC) and the mesencephalic reticular formation (MRF) in the control of combined head and eye movements (i.e., gaze). Recent microstimulation, single-cell recording, and lesion experiments are reviewed in which monkeys are free to move their heads. Cells in the SC discharge in advance of combined head and eye movements and most likely provide a gaze error signal to downstream structures. In contrast, the neurons in the MRF are of at least two types. Eye cells have features that are similar to neurons in the rostral portion of the SC, but fire before the onset of horizontal eye movments. A second group of MRF neurons begin to fire after the onset of the gaze shift and are most closely associated with movements of the head. The peak discharge of these late-onset MRF neurons occurs near the peak head velocity. Stimulation in the rostral SC generates eye movements with fixed amplitude and direction. A similar response is noted after stimulation of the more dorsal portion of the caudal MRF. Stimulation in the caudal portion of the SC produces combined head and eye movements of fixed amplitude. Electrical activation of the more ventral portions of the caudal MRF generates goal-directed and centering eye movements. Temporary inactivation of the SC with the GABA agonist muscimol generated hypometria and curved trajectories of contralateral eye movements. Inactivation of the caudal MRF produced contralateral hypermetria and ipsilateral hypometria of saccades. Release of the monkey's head demonstrated a profound contralateral head tilt. Taken together, these data suggest that the gaze signal generated in the SC is filtered by neurons in the MRF to generate a feedback signal of eye motor error. The head signal found in the MRF could cancel a portion of the gaze signal coming from the SC in the form of head velocity feedback.

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Year:  2002        PMID: 11960798     DOI: 10.1111/j.1749-6632.2002.tb02813.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  7 in total

1.  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

2.  Anatomical evidence for interconnections between the central mesencephalic reticular formation and cervical spinal cord in the cat and macaque.

Authors:  Susan Warren; David M Waitzman; Paul J May
Journal:  Anat Rec (Hoboken)       Date:  2008-02       Impact factor: 2.064

3.  Temporal characteristics of neurons in the central mesencephalic reticular formation of head unrestrained monkeys.

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

4.  Connectivity of the goldfish optic tectum with the mesencephalic and rhombencephalic reticular formation.

Authors:  M P Pérez-Pérez; M A Luque; L Herrero; P A Nunez-Abades; B Torres
Journal:  Exp Brain Res       Date:  2003-05-14       Impact factor: 1.972

5.  Saccade trajectories evoked by sequential and colliding stimulation of the monkey superior colliculus.

Authors:  Christopher T Noto; James W Gnadt
Journal:  Brain Res       Date:  2009-07-29       Impact factor: 3.252

6.  Delineation of motoneuron subgroups supplying individual eye muscles in the human oculomotor nucleus.

Authors:  Emmanuel Che Ngwa; Christina Zeeh; Ahmed Messoudi; Jean A Büttner-Ennever; Anja K E Horn
Journal:  Front Neuroanat       Date:  2014-02-12       Impact factor: 3.856

7.  Organization of the inputs and outputs of the mouse superior colliculus.

Authors:  Nora L Benavidez; Michael S Bienkowski; Muye Zhu; Luis H Garcia; Marina Fayzullina; Lei Gao; Ian Bowman; Lin Gou; Neda Khanjani; Kaelan R Cotter; Laura Korobkova; Marlene Becerra; Chunru Cao; Monica Y Song; Bin Zhang; Seita Yamashita; Amanda J Tugangui; Brian Zingg; Kasey Rose; Darrick Lo; Nicholas N Foster; Tyler Boesen; Hyun-Seung Mun; Sarvia Aquino; Ian R Wickersham; Giorgio A Ascoli; Houri Hintiryan; Hong-Wei Dong
Journal:  Nat Commun       Date:  2021-06-28       Impact factor: 14.919

  7 in total

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