Literature DB >> 8713453

Responses of neurons of the nucleus of the optic tract and the dorsal terminal nucleus of the accessory optic tract in the awake monkey.

U J Ilg1, K P Hoffmann.   

Abstract

The nucleus of the optic tract (NOT) and the dorsal terminal nucleus of the accessory optic tract (DTN) are essential nuclei for the generation of slow-phase eye movements during horizontal optokinetic nystagmus. We recorded from 101 neurons (all directionally selective) in four NOT/DTN of three trained and behaving rhesus monkeys. Neuronal activity increased when stimuli moved ipsiversively with respect to the recording site and decreased below spontaneous activity when stimuli moved contraversively. While the monkey fixated a small spot, some NOT/DTN neurons did not respond at all to the retinal image slip of a whole-field random dot pattern; others showed a monotonic increase of activity to increasing velocities of that stimulus. The velocity range tested was up to 100 degrees/s. During the execution of optokinetic nystagmus, 39 of 73 cells tested showed a velocity-tuned response with an average optimum at 21 degrees/s retinal image slip. Following saccades during optokinetic nystagmus (quick phases), the NOT/DTN neuronal activity briefly attained the level of spontaneous activity, as predicted from the velocity selectivity during optokinetic nystagmus. Immediately upon cessation of optokinetic stimulation in the preferred direction, NOT/DTN activity returned to the spontaneous level and did not reflect the ongoing optokinetic afternystagmus in darkness. Most NOT/DTN neurons displayed direction selectivity also during smooth pursuit. Twenty-one of 50 cells tested (42%) always responded to the retinal slip of the target (target velocity cells), 16 cells (32%) responded to the retinal slip of the background (background velocity cells), and 13 cells (26%) did not respond at all during smooth pursuit. We conclude from our results that the NOT/DTN is an essential structure for the processing of the direction and speed of retinal image slip. This information is then used for the generation and maintenance of slow eye movements, preferentially during horizontal optokinetic nystagmus but also during pursuit eye movements.

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Year:  1996        PMID: 8713453     DOI: 10.1111/j.1460-9568.1996.tb01170.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  10 in total

1.  Brainstem and cerebellar fMRI-activation during horizontal and vertical optokinetic stimulation.

Authors:  Sandra Bense; Barbara Janusch; Goran Vucurevic; Thomas Bauermann; Peter Schlindwein; Thomas Brandt; Peter Stoeter; Marianne Dieterich
Journal:  Exp Brain Res       Date:  2006-04-25       Impact factor: 1.972

2.  Optogenetic localization and genetic perturbation of saccade-generating neurons in zebrafish.

Authors:  Peter J Schoonheim; Aristides B Arrenberg; Filippo Del Bene; Herwig Baier
Journal:  J Neurosci       Date:  2010-05-19       Impact factor: 6.167

3.  Motion integration for ocular pursuit does not hinder perceptual segregation of moving objects.

Authors:  Zhenlan Jin; Scott N J Watamaniuk; Aarlenne Z Khan; Elena Potapchuk; Stephen J Heinen
Journal:  J Neurosci       Date:  2014-04-23       Impact factor: 6.167

4.  An fMRI study of optokinetic nystagmus and smooth-pursuit eye movements in humans.

Authors:  Christina S Konen; Raimund Kleiser; Rüdiger J Seitz; Frank Bremmer
Journal:  Exp Brain Res       Date:  2005-04-29       Impact factor: 1.972

5.  Responses of primate area MT during the execution of optokinetic nystagmus and afternystagmus.

Authors:  U J Ilg
Journal:  Exp Brain Res       Date:  1997-02       Impact factor: 1.972

6.  Nonvisual complex spike signals in the rabbit cerebellar flocculus.

Authors:  Beerend H J Winkelman; Tim Belton; Minah Suh; Michiel Coesmans; Menno M Morpurgo; John I Simpson
Journal:  J Neurosci       Date:  2014-02-26       Impact factor: 6.167

7.  Elimination of climbing fiber instructive signals during motor learning.

Authors:  Michael C Ke; Cong C Guo; Jennifer L Raymond
Journal:  Nat Neurosci       Date:  2009-08-16       Impact factor: 24.884

8.  Expansion of visual space during optokinetic afternystagmus (OKAN).

Authors:  André Kaminiarz; Bart Krekelberg; Frank Bremmer
Journal:  J Neurophysiol       Date:  2008-02-27       Impact factor: 2.714

9.  Forward models and state estimation in compensatory eye movements.

Authors:  Maarten A Frens; Opher Donchin
Journal:  Front Cell Neurosci       Date:  2009-11-23       Impact factor: 5.505

10.  Spontaneous activity of rat pretectal nuclear complex neurons in vitro.

Authors:  Nora Prochnow; Matthias Schmidt
Journal:  BMC Neurosci       Date:  2004-08-27       Impact factor: 3.288

  10 in total

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