Literature DB >> 33139553

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

Julie Quinet1, Kevin Schultz2, Paul J May3,4,5, Paul D Gamlin2.   

Abstract

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.

Entities:  

Keywords:  binocular control; neural recordings; oculomotor; saccades; vergence

Mesh:

Year:  2020        PMID: 33139553      PMCID: PMC7682339          DOI: 10.1073/pnas.2015318117

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  54 in total

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2.  Responses of cells in the midbrain near-response area in monkeys with strabismus.

Authors:  Vallabh E Das
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-06-22       Impact factor: 4.799

Review 3.  Neuronal circuitry controlling the near response.

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4.  Binocular Eye Movements Are Adapted to the Natural Environment.

Authors:  Agostino Gibaldi; Martin S Banks
Journal:  J Neurosci       Date:  2019-02-07       Impact factor: 6.167

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

Authors:  Julie Quinet; Kevin Schultz; Paul J May; Paul D Gamlin
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-02       Impact factor: 11.205

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Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

8.  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

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Journal:  Vision Res       Date:  1978       Impact factor: 1.886

10.  A central mesencephalic reticular formation projection to medial rectus motoneurons supplying singly and multiply innervated extraocular muscle fibers.

Authors:  Martin O Bohlen; Susan Warren; Paul J May
Journal:  J Comp Neurol       Date:  2017-03-14       Impact factor: 3.215

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  10 in total

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

Authors:  Julie Quinet; Kevin Schultz; Paul J May; Paul D Gamlin
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-02       Impact factor: 11.205

2.  Is the central mesencephalic reticular formation a purely horizontal gaze center?

Authors:  Martin O Bohlen; Susan Warren; Paul J May
Journal:  Brain Struct Funct       Date:  2022-07-24       Impact factor: 3.748

3.  Alteration of Degree Centrality in Adolescents With Early Blindness.

Authors:  Zhi Wen; Yan Kang; Yu Zhang; Huaguang Yang; Baojun Xie
Journal:  Front Hum Neurosci       Date:  2022-06-27       Impact factor: 3.473

4.  Stochastic Physiological Gaze-Evoked Nystagmus With Slow Centripetal Drift During Fixational Eye Movements at Small Gaze Eccentricities.

Authors:  Makoto Ozawa; Yasuyuki Suzuki; Taishin Nomura
Journal:  Front Hum Neurosci       Date:  2022-05-12       Impact factor: 3.473

5.  Cerebellar projections to the macaque midbrain tegmentum: Possible near response connections.

Authors:  Martin O Bohlen; Paul D Gamlin; Susan Warren; Paul J May
Journal:  Vis Neurosci       Date:  2021-05-12       Impact factor: 3.241

6.  A Novel Tectal/Pretectal Population of Premotor Lens Accommodation Neurons.

Authors:  Paul J May; Paul D Gamlin; Susan Warren
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-01-03       Impact factor: 4.799

7.  Input and output organization of the mesodiencephalic junction for cerebro-cerebellar communication.

Authors:  Xiaolu Wang; Manuele Novello; Zhenyu Gao; Tom J H Ruigrok; Chris I De Zeeuw
Journal:  J Neurosci Res       Date:  2021-12-01       Impact factor: 4.433

8.  Large-scale cortico-cerebellar computations for horizontal and vertical vergence in humans.

Authors:  Hiroyuki Mitsudo; Naruhito Hironaga; Katsuya Ogata; Shozo Tobimatsu
Journal:  Sci Rep       Date:  2022-07-08       Impact factor: 4.996

9.  A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain.

Authors:  Claire Leyden; Christian Brysch; Aristides B Arrenberg
Journal:  Sci Rep       Date:  2021-06-16       Impact factor: 4.379

10.  Intrinsic bursts facilitate learning of Lévy flight movements in recurrent neural network models.

Authors:  Morihiro Ohta; Toshitake Asabuki; Tomoki Fukai
Journal:  Sci Rep       Date:  2022-03-23       Impact factor: 4.379

  10 in total

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