Literature DB >> 14985893

Electrical stimulation of rhesus monkey nucleus reticularis gigantocellularis. I. Characteristics of evoked head movements.

Stephan Quessy1, Edward G Freedman.   

Abstract

The nucleus reticularis gigantocellularis (NRG) receives monosynaptic input from the superior colliculus (SC) and projects directly to neck motor neuron pools. Neurons in NRG are well situated to play a critical role in transforming SC signals into head movement commands. A previous study of movements evoked by NRG stimulation in the primate reported a variety of ipsilateral and contralateral head movements with horizontal, vertical and torsional components. In addition to head movements, it was reported that NRG stimulation could evoke movements of the pinnae, face, upper torso, and co-contraction of neck muscles. In this report, the role of the rhesus monkey NRG in head movement control was investigated using electrical stimulation of the rostral portion of the NRG. The goal was to characterize head movements evoked by NRG stimulation, describe the effects of altering stimulation parameters, and assess the relative movements of the eyes and head. Results indicate that electrical stimulation in the rostral portion of the NRG of the primate can consistently evoke ipsilateral head rotations in the horizontal plane. Head movement amplitude and peak velocity depend upon stimulation parameters (primarily frequency and duration of stimulation trains). During stimulation-induced head movements the eyes counter-rotate (presumably a result of the vestibulo-ocular reflex: VOR). At 46 stimulation sites from two subjects the average gain of this counter-rotation was -0.38 (+/-0.18). After the end of the stimulation train the head generally continued to move. During this epoch, after electrical stimulation ceased, VOR gain remained at this reduced level. In addition, VOR gain was similarly low when electrical stimulation was carried out during active fixation of a visual target. These data extend existing descriptions of head movements evoked by electrical stimulation of the NRG, and add to the understanding of the role of this structure in producing head movements.

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Year:  2004        PMID: 14985893     DOI: 10.1007/s00221-003-1787-8

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


  47 in total

1.  Coordination of the eyes and head: movement kinematics.

Authors:  E G Freedman; D L Sparks
Journal:  Exp Brain Res       Date:  2000-03       Impact factor: 1.972

2.  Interactions between eye and head control signals can account for movement kinematics.

Authors:  E G Freedman
Journal:  Biol Cybern       Date:  2001-06       Impact factor: 2.086

3.  The superior colliculus encodes gaze commands in retinal coordinates.

Authors:  E M Klier; H Wang; J D Crawford
Journal:  Nat Neurosci       Date:  2001-06       Impact factor: 24.884

4.  Activity of cells in the deeper layers of the superior colliculus of the rhesus monkey: evidence for a gaze displacement command.

Authors:  E G Freedman; D L Sparks
Journal:  J Neurophysiol       Date:  1997-09       Impact factor: 2.714

5.  Combined eye-head gaze shifts in the primate. I. Metrics.

Authors:  R D Tomlinson; P S Bahra
Journal:  J Neurophysiol       Date:  1986-12       Impact factor: 2.714

6.  Geometric adjustments to account for eye eccentricity in processing horizontal and vertical eye and head movement data.

Authors:  W P Huebner; W H Paloski; M F Reschke; J J Bloomberg
Journal:  J Vestib Res       Date:  1995 Jul-Aug       Impact factor: 2.435

7.  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

8.  Gaze-related activity of putative inhibitory burst neurons in the head-free cat.

Authors:  K E Cullen; D Guitton; C G Rey; W Jiang
Journal:  J Neurophysiol       Date:  1993-12       Impact factor: 2.714

9.  Projections of the superior colliculus to the supraspinal nucleus and the cervical spinal cord gray of the cat.

Authors:  M F Huerta; J K Harting
Journal:  Brain Res       Date:  1982-06-24       Impact factor: 3.252

10.  Patterns of projection and braching of reticulospinal neurons.

Authors:  B W Peterson; R A Maunz; N G Pitts; R G Mackel
Journal:  Exp Brain Res       Date:  1975-10-24       Impact factor: 1.972

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  29 in total

1.  Electrical stimulation of rhesus monkey nucleus reticularis gigantocellularis. II. Effects on metrics and kinematics of ongoing gaze shifts to visual targets.

Authors:  Edward G Freedman; Stephan Quessy
Journal:  Exp Brain Res       Date:  2004-02-21       Impact factor: 1.972

2.  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

3.  Overlapping gaze shifts reveal timing of an eye-head gate.

Authors:  Brian S Oommen; John S Stahl
Journal:  Exp Brain Res       Date:  2005-07-21       Impact factor: 1.972

4.  Bilateral actions of the reticulospinal tract on arm and shoulder muscles in the monkey: stimulus triggered averaging.

Authors:  Adam G Davidson; John A Buford
Journal:  Exp Brain Res       Date:  2006-02-28       Impact factor: 1.972

5.  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

6.  Effect of reversible inactivation of superior colliculus on head movements.

Authors:  Mark M G Walton; Bernard Bechara; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2008-02-27       Impact factor: 2.714

7.  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

8.  Eye-head coupling tendencies in stationary and moving subjects.

Authors:  Zachary C Thumser; John S Stahl
Journal:  Exp Brain Res       Date:  2009-04-26       Impact factor: 1.972

9.  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

10.  Eye-head coordination in moderately affected Huntington's Disease patients: do head movements facilitate gaze shifts?

Authors:  W Becker; R Jürgens; J Kassubek; D Ecker; B Kramer; B Landwehrmeyer
Journal:  Exp Brain Res       Date:  2008-09-20       Impact factor: 1.972

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