Literature DB >> 23076111

Short-term saccadic adaptation in the macaque monkey: a binocular mechanism.

K P Schultz1, C Busettini.   

Abstract

Saccadic eye movements are rapid transfers of gaze between objects of interest. Their duration is too short for the visual system to be able to follow their progress in time. Adaptive mechanisms constantly recalibrate the saccadic responses by detecting how close the landings are to the selected targets. The double-step saccadic paradigm is a common method to simulate alterations in saccadic gain. While the subject is responding to a first target shift, a second shift is introduced in the middle of this movement, which masks it from visual detection. The error in landing introduced by the second shift is interpreted by the brain as an error in the programming of the initial response, with gradual gain changes aimed at compensating the apparent sensorimotor mismatch. A second shift applied dichoptically to only one eye introduces disconjugate landing errors between the two eyes. A monocular adaptive system would independently modify only the gain of the eye exposed to the second shift in order to reestablish binocular alignment. Our results support a binocular mechanism. A version-based saccadic adaptive process detects postsaccadic version errors and generates compensatory conjugate gain alterations. A vergence-based saccadic adaptive process detects postsaccadic disparity errors and generates corrective nonvisual disparity signals that are sent to the vergence system to regain binocularity. This results in striking dynamical similarities between visually driven combined saccade-vergence gaze transfers, where the disparity is given by the visual targets, and the double-step adaptive disconjugate responses, where an adaptive disparity signal is generated internally by the saccadic system.

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Year:  2012        PMID: 23076111      PMCID: PMC3545465          DOI: 10.1152/jn.01013.2011

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  114 in total

1.  Saccadic dysmetria and adaptation after lesions of the cerebellar cortex.

Authors:  S Barash; A Melikyan; A Sivakov; M Zhang; M Glickstein; P Thier
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

2.  Flexibility of saccade adaptation in the monkey: different gain states for saccades in the same direction.

Authors:  S Watanabe; C T Noto; A F Fuchs
Journal:  Exp Brain Res       Date:  2000-01       Impact factor: 1.972

3.  Saccade amplitude disconjugacy induced by aniseikonia: role of monocular depth cues.

Authors:  M Pia Bucci; Z Kapoula; T Eggert
Journal:  Vision Res       Date:  1999-09       Impact factor: 1.886

4.  Relation between the metrics of the presaccadic attention shift and of the saccade before and after saccadic adaptation.

Authors:  J Ditterich; T Eggert; A Straube
Journal:  J Neurophysiol       Date:  2000-10       Impact factor: 2.714

5.  Discharge properties of neurons in the rostral superior colliculus of the monkey during smooth-pursuit eye movements.

Authors:  R J Krauzlis; M A Basso; R H Wurtz
Journal:  J Neurophysiol       Date:  2000-08       Impact factor: 2.714

6.  Conjugate and vergence oscillations during saccades and gaze shifts: implications for integrated control of binocular movement.

Authors:  Pierre A Sylvestre; Henrietta L Galiana; Kathleen E Cullen
Journal:  J Neurophysiol       Date:  2002-01       Impact factor: 2.714

7.  Evidence that the superior colliculus participates in the feedback control of saccadic eye movements.

Authors:  Robijanto Soetedjo; Chris R S Kaneko; Albert F Fuchs
Journal:  J Neurophysiol       Date:  2002-02       Impact factor: 2.714

8.  Extraretinal inputs to neurons in the rostral superior colliculus of the monkey during smooth-pursuit eye movements.

Authors:  R J Krauzlis
Journal:  J Neurophysiol       Date:  2001-11       Impact factor: 2.714

9.  Role of the cerebellar posterior interpositus nucleus in saccades I. Effect of temporary lesions.

Authors:  F R Robinson
Journal:  J Neurophysiol       Date:  2000-09       Impact factor: 2.714

10.  Partial ablations of the flocculus and ventral paraflocculus in monkeys cause linked deficits in smooth pursuit eye movements and adaptive modification of the VOR.

Authors:  H Rambold; A Churchland; Y Selig; L Jasmin; S G Lisberger
Journal:  J Neurophysiol       Date:  2002-02       Impact factor: 2.714

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  6 in total

1.  Vertical and oblique saccade disconjugacy in strabismus.

Authors:  Mark M G Walton; Seiji Ono; Michael Mustari
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-01-13       Impact factor: 4.799

2.  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

3.  Activity of near-response cells during disconjugate saccades in strabismic monkeys.

Authors:  Adam Pallus; Mark M G Walton; Michael Mustari
Journal:  J Neurophysiol       Date:  2018-08-15       Impact factor: 2.714

4.  Cerebellar transcranial direct current stimulation effects on saccade adaptation.

Authors:  Eric Avila; Jos N van der Geest; Sandra Kengne Kamga; M Claire Verhage; Opher Donchin; Maarten A Frens
Journal:  Neural Plast       Date:  2015-03-02       Impact factor: 3.599

5.  Monocular and Binocular Contributions to Oculomotor Plasticity.

Authors:  Guido Maiello; William J Harrison; Peter J Bex
Journal:  Sci Rep       Date:  2016-08-18       Impact factor: 4.379

6.  Perceptual effects of unequal saccadic adaptation produced by a dichoptic step.

Authors:  Anna Kosovicheva; Peter J Bex
Journal:  J Vis       Date:  2020-05-11       Impact factor: 2.240

  6 in total

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