Literature DB >> 18458891

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

Neeraj J Gandhi1, Ellen J Barton, David L Sparks.   

Abstract

Constant frequency microstimulation of the paramedian pontine reticular formation (PPRF) in head-restrained monkeys evokes a constant velocity eye movement. Since the PPRF receives significant projections from structures that control coordinated eye-head movements, we asked whether stimulation of the pontine reticular formation in the head-unrestrained animal generates a combined eye-head movement or only an eye movement. Microstimulation of most sites yielded a constant-velocity gaze shift executed as a coordinated eye-head movement, although eye-only movements were evoked from some sites. The eye and head contributions to the stimulation-evoked movements varied across stimulation sites and were drastically different from the lawful relationship observed for visually-guided gaze shifts. These results indicate that the microstimulation activated elements that issued movement commands to the extraocular and, for most sites, neck motoneurons. In addition, the stimulation-evoked changes in gaze were similar in the head-restrained and head-unrestrained conditions despite the assortment of eye and head contributions, suggesting that the vestibulo-ocular reflex (VOR) gain must be near unity during the coordinated eye-head movements evoked by stimulation of the PPRF. These findings contrast the attenuation of VOR gain associated with visually-guided gaze shifts and suggest that the vestibulo-ocular pathway processes volitional and PPRF stimulation-evoked gaze shifts differently.

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Year:  2008        PMID: 18458891      PMCID: PMC3655330          DOI: 10.1007/s00221-008-1401-1

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


  68 in total

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Authors:  L Ling; A F Fuchs; J O Phillips; E G Freedman
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2.  Conceptual issues related to the role of the superior colliculus in the control of gaze.

Authors:  D L Sparks
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3.  Contribution of the frontal eye field to gaze shifts in the head-unrestrained monkey: effects of microstimulation.

Authors:  Thomas A Knight; Albert F Fuchs
Journal:  J Neurophysiol       Date:  2006-10-25       Impact factor: 2.714

4.  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

5.  The proprioceptive representation of eye position in monkey primary somatosensory cortex.

Authors:  Xiaolan Wang; Mingsha Zhang; Ian S Cohen; Michael E Goldberg
Journal:  Nat Neurosci       Date:  2007-04-01       Impact factor: 24.884

6.  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

7.  Stimulation of the superior colliculus in the alert cat. II. Eye and head movements evoked when the head is unrestrained.

Authors:  A Roucoux; D Guitton; M Crommelinck
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

8.  Stimulation of the superior colliculus in the alert cat. I. Eye movements and neck EMG activity evoked when the head is restrained.

Authors:  D Guitton; M Crommelinck; A Roucoux
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

9.  A quantitative analysis of generation of saccadic eye movements by burst neurons.

Authors:  J A Van Gisbergen; D A Robinson; S Gielen
Journal:  J Neurophysiol       Date:  1981-03       Impact factor: 2.714

10.  Spinal projections from the lower brain stem in the cat as demonstrated by the horseradish peroxidase technique. I. Origins of the reticulospinal tracts and their funicular trajectories.

Authors:  M Tohyama; K Sakai; D Salvert; M Touret; M Jouvet
Journal:  Brain Res       Date:  1979-09-21       Impact factor: 3.252

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  15 in total

1.  The relative impact of microstimulation parameters on movement generation.

Authors:  Husam A Katnani; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2012-04-25       Impact factor: 2.714

2.  Revealing the kinematics of the oculomotor plant with tertiary eye positions and ocular counterroll.

Authors:  Eliana M Klier; Hui Meng; Dora E Angelaki
Journal:  J Neurophysiol       Date:  2010-11-24       Impact factor: 2.714

3.  Dynamics of primate oculomotor plant revealed by effects of abducens microstimulation.

Authors:  Sean R Anderson; John Porrill; Sokratis Sklavos; Neeraj J Gandhi; David L Sparks; Paul Dean
Journal:  J Neurophysiol       Date:  2009-03-18       Impact factor: 2.714

4.  Stimulation of pontine reticular formation in monkeys with strabismus.

Authors:  Mark M G Walton; Seiji Ono; Michael J Mustari
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-10-29       Impact factor: 4.799

5.  Activity of long-lead burst neurons in pontine reticular formation during head-unrestrained gaze shifts.

Authors:  Mark M G Walton; Edward G Freedman
Journal:  J Neurophysiol       Date:  2013-10-30       Impact factor: 2.714

6.  Cerebellar control of saccade dynamics: contribution of the fastigial oculomotor region.

Authors:  Julie Quinet; Laurent Goffart
Journal:  J Neurophysiol       Date:  2015-03-04       Impact factor: 2.714

Review 7.  Distinct neural circuits for control of movement vs. holding still.

Authors:  Reza Shadmehr
Journal:  J Neurophysiol       Date:  2017-01-04       Impact factor: 2.714

8.  Instantaneous Midbrain Control of Saccade Velocity.

Authors:  Ivan Smalianchuk; Uday K Jagadisan; Neeraj J Gandhi
Journal:  J Neurosci       Date:  2018-10-05       Impact factor: 6.167

9.  Abnormal tuning of saccade-related cells in pontine reticular formation of strabismic monkeys.

Authors:  Mark M G Walton; Michael J Mustari
Journal:  J Neurophysiol       Date:  2015-06-10       Impact factor: 2.714

Review 10.  The vestibular system: multimodal integration and encoding of self-motion for motor control.

Authors:  Kathleen E Cullen
Journal:  Trends Neurosci       Date:  2012-01-12       Impact factor: 13.837

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