Neural Control of Eye Movements

Neural Control of Visually Guided Eye Movements

Neuroadaptive Systems ◽

10.1201/b13019-10 ◽

2012 ◽

pp. 111-152 ◽

Cited By ~ 2

Keyword(s):

Eye Movements ◽

Neural Control ◽

Visually Guided

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Saccade, search and orient - the neural control of saccadic eye movements

European Journal of Neuroscience ◽

10.1111/j.1460-9568.2011.07810.x ◽

2011 ◽

Vol 34 (1) ◽

pp. 176-176

Author(s):

Douglas P. Munoz ◽

Brian C. Coe

Keyword(s):

Eye Movements ◽

Neural Control ◽

Saccadic Eye Movements

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The influence of eye muscle surgery on shape and relative orientation of displacement planes: Indirect evidence for neural control of 3D eye movements

Strabismus ◽

10.1076/stra.10.3.199.8124 ◽

2002 ◽

Vol 10 (3) ◽

pp. 199-209 ◽

Cited By ~ 2

Author(s):

J. Bosman ◽

M.P.M. ten Tusscher ◽

I. de Jong ◽

J.S.H. Vles ◽

H. Kingma

Keyword(s):

Eye Movements ◽

Neural Control ◽

Indirect Evidence ◽

Relative Orientation ◽

Eye Muscle ◽

Eye Muscle Surgery

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The Neural Control of Visually Guided Eye Movements

Cognitive Neuroscience of Attention ◽

10.4324/9781410603906-7 ◽

1998 ◽

pp. 13-60

Keyword(s):

Eye Movements ◽

Neural Control ◽

Visually Guided

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Central Positional Nystagmus Simulated by a Mathematical Ocular Motor Model of Otolith-Dependent Modification of Listing's Plane

Journal of Neurophysiology ◽

10.1152/jn.2001.86.4.1546 ◽

2001 ◽

Vol 86 (4) ◽

pp. 1546-1554 ◽

Cited By ~ 30

Author(s):

S. Glasauer ◽

M. Dieterich ◽

Th. Brandt

Keyword(s):

Eye Movements ◽

Neural Control ◽

Position Control ◽

Three Dimensional ◽

Head Tilt ◽

Eye Position ◽

Positional Nystagmus ◽

Listing's Plane ◽

Head Positions ◽

Listing’S Plane

To find an explanation of the mechanisms of central positional nystagmus in neurological patients with posterior fossa lesions, we developed a three-dimensional (3-D) mathematical model to simulate head position-dependent changes in eye position control relative to gravity. This required a model implementation of saccadic burst generation, of the neural velocity to eye position integrator, which includes the experimentally demonstrated leakage in the torsional component, and of otolith-dependent neural control of Listing's plane. The validity of the model was first tested by simulating saccadic eye movements in different head positions. Then the model was used to simulate central positional nystagmus in off-vertical head positions. The model simulated lesions of assumed otolith inputs to the burst generator or the neural integrator, both of which resulted in different types of torsional-vertical nystagmus that only occurred during head tilt in roll plane. The model data qualitatively fit clinical observations of central positional nystagmus. Quantitative comparison with patient data were not possible, since no 3-D analyses of eye movements in various head positions have been reported in the literature on patients with positional nystagmus. The present model, prompted by an open clinical question, proposes a new hypothesis about the generation of pathological nystagmus and about neural control of Listing's plane.

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Neural control of rapid binocular eye movements: Saccade-vergence burst neurons

Proceedings of the National Academy of Sciences ◽

10.1073/pnas.2015318117 ◽

2020 ◽

Vol 117 (46) ◽

pp. 29123-29132 ◽

Cited By ~ 1

Author(s):

Julie Quinet ◽

Kevin Schultz ◽

Paul J. May ◽

Paul D. Gamlin

Keyword(s):

Eye Movements ◽

Neural Control ◽

Three Dimensional ◽

Mesencephalic Reticular Formation ◽

Burst Neurons ◽

Central Mesencephalic Reticular Formation ◽

3D Space ◽

Modeling Studies ◽

Premotor Neurons ◽

Highly Correlated

During normal viewing, we direct our eyes between objects in three-dimensional (3D) space many times a minute. To accurately fixate these objects, which are usually located in different directions and at different distances, we must generate eye movements with appropriate versional and vergence components. These combined saccade-vergence eye movements result in disjunctive saccades with a vergence component that is much faster than that generated during smooth, symmetric vergence eye movements. The neural control of disjunctive saccades is still poorly understood. Recent anatomical studies suggested that the central mesencephalic reticular formation (cMRF), located lateral to the oculomotor nucleus, contains premotor neurons potentially involved in the neural control of these eye movements. We have therefore investigated the role of the cMRF in the control of disjunctive saccades in trained rhesus monkeys. Here, we describe a unique population of cMRF neurons that, during disjunctive saccades, display a burst of spikes that are highly correlated with vergence velocity. Importantly, these neurons show no increase in activity for either conjugate saccades or symmetric vergence. These neurons are termed saccade-vergence burst neurons (SVBNs) to maintain consistency with modeling studies that proposed that such a class of neuron exists to generate the enhanced vergence velocities observed during disjunctive saccades. Our results demonstrate the existence and characteristics of SVBNs whose activity is correlated solely with the vergence component of disjunctive saccades and, based on modeling studies, are critically involved in the generation of the disjunctive saccades required to view objects in our 3D world.

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