Literature DB >> 3559999

Mossy fibres sending retinal-slip, eye, and head velocity signals to the flocculus of the monkey.

H Noda.   

Abstract

Discharges of mossy fibres were recorded from the cerebellar flocculus of monkeys trained to fixate a small visual target and to track the target when it moved slowly. The experimental paradigms used were designed to study neural responses to retinal-slip velocity, eye velocity, or head velocity, individually or in combination. Among 485 mossy-fibre units recorded from the flocculus, sixty-four units (or 13%) responded to movement of the visual stimulus in the horizontal plane. Two distinct groups of visual mossy fibres were found: they were designated 'visual units' (thirty-nine/sixty-four units or 61%) and 'visuomotor units' (twenty-five/sixty-four units or 39%). The visual units responded exclusively to the retinal-slip velocity. Stationary fixation was necessary for clear cyclic modulation of activity. Their responses declined when the retinal-slip velocity was reduced by eye movements in the same direction. The responses of the visual units were directionally selective and lagged behind the occurrence of 'turnabouts' (changes in direction of stimulus movement) and their peak discharges also lagged the occurrence of peak velocity. Each visual unit had a limited range of velocity sensitivity; in some units the range covered the velocity range of smooth-pursuit eye movements. The visuomotor units had visual receptive fields in the peripheral retina (outside of the central 10 deg); they received also oculomotor and vestibular signals. When the head was stationary, the visuomotor units responded to the target velocity (or visual stimulus velocity) which is the algebraic sum of the retinal-slip velocity and the eye velocity. Their responses reflected the retinal-slip velocity during stationary fixation and the eye velocity during smooth-pursuit eye movements. The responses to stimulus movements were, therefore, almost identical regardless of whether the eyes remained stationary or moved with the stimulus. In response to sinusoidal stimulus movements, the responses of the visuomotor units frequently preceded the stimulus velocity, and the phase lead relative to the velocity curve increased when the frequency of sinusoidal movements was increased. This reflected a relatively constant lead of neural discharges (circa 125 ms) during various frequencies. When the head was moved, the responses of the visuomotor units were dominated by the head velocity, and discharges in response either to the retinal-slip velocity or to the eye velocity (both in the direction opposite to the head velocity) were occluded.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1986        PMID: 3559999      PMCID: PMC1182884          DOI: 10.1113/jphysiol.1986.sp016240

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  28 in total

1.  Visual tracking and the primate flocculus.

Authors:  F A Miles; J H Fuller
Journal:  Science       Date:  1975-09-19       Impact factor: 47.728

2.  Afferents to the vestibulo-cerebellum and the origin of the visual climbing fibers in the rabbit.

Authors:  K Alley; R Baker; J I Simpson
Journal:  Brain Res       Date:  1975-11-21       Impact factor: 3.252

3.  Direct accessory optic projections to the vestibulo-cerebellum: a possible channel for oculomotor control systems.

Authors:  S E Brauth
Journal:  Exp Brain Res       Date:  1977-05-23       Impact factor: 1.972

4.  Climbing fiber activation of Purkinje cells in the flocculus by impulses transferred through the visual pathway.

Authors:  K Maekawa; J I Simpson
Journal:  Brain Res       Date:  1972-04-14       Impact factor: 3.252

5.  Neuronal activity in the vestibular nuclei of the alert monkey during vestibular and optokinetic stimulation.

Authors:  W Waespe; V Henn
Journal:  Exp Brain Res       Date:  1977-04-21       Impact factor: 1.972

6.  Vestibular nucleus units in alert monkeys are also influenced by moving visual fields.

Authors:  V Henn; L R Young; C Finley
Journal:  Brain Res       Date:  1974-05-10       Impact factor: 3.252

7.  Single unit firing patterns in the vestibular nuclei related to voluntary eye movements and passive body rotation in conscious monkeys.

Authors:  F A Miles
Journal:  Brain Res       Date:  1974-05-17       Impact factor: 3.252

8.  Role of primate flocculus during rapid behavioral modification of vestibuloocular reflex. II. Mossy fiber firing patterns during horizontal head rotation and eye movement.

Authors:  S G Lisberger; A F Fuchs
Journal:  J Neurophysiol       Date:  1978-05       Impact factor: 2.714

9.  Role of primate flocculus during rapid behavioral modification of vestibuloocular reflex. I. Purkinje cell activity during visually guided horizontal smooth-pursuit eye movements and passive head rotation.

Authors:  S G Lisberger; A F Fuchs
Journal:  J Neurophysiol       Date:  1978-05       Impact factor: 2.714

10.  Afferents to the flocculus of the cerebellum in the rhesus macaque as revealed by retrograde transport of horseradish peroxidase.

Authors:  T Langer; A F Fuchs; C A Scudder; M C Chubb
Journal:  J Comp Neurol       Date:  1985-05-01       Impact factor: 3.215

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  13 in total

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Authors:  G R Barnes; P T Asselman
Journal:  J Physiol       Date:  1991-08       Impact factor: 5.182

2.  A 'tachometer' feedback model of smooth pursuit eye movements.

Authors:  D L Ringach
Journal:  Biol Cybern       Date:  1995-11       Impact factor: 2.086

3.  Golgi cells operate as state-specific temporal filters at the input stage of the cerebellar cortex.

Authors:  Shane A Heine; Stephen M Highstein; Pablo M Blazquez
Journal:  J Neurosci       Date:  2010-12-15       Impact factor: 6.167

4.  Diverse precerebellar neurons share similar intrinsic excitability.

Authors:  Kristine E Kolkman; Lauren E McElvain; Sascha du Lac
Journal:  J Neurosci       Date:  2011-11-16       Impact factor: 6.167

5.  Neuronal activity in the flocculus of the alert monkey during sinusoidal optokinetic stimulation.

Authors:  G Markert; U Büttner; A Straube; R Boyle
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

6.  Factors affecting the predictability of pseudo-random motion stimuli in the pursuit reflex of man.

Authors:  G R Barnes; C J Ruddock
Journal:  J Physiol       Date:  1989-01       Impact factor: 5.182

7.  Volitional control of anticipatory ocular pursuit responses under stabilised image conditions in humans.

Authors:  G Barnes; S Goodbody; S Collins
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

Review 8.  Internal models of eye movement in the floccular complex of the monkey cerebellum.

Authors:  S G Lisberger
Journal:  Neuroscience       Date:  2009-03-29       Impact factor: 3.590

9.  Gating of neural error signals during motor learning.

Authors:  Rhea R Kimpo; Jacob M Rinaldi; Christina K Kim; Hannah L Payne; Jennifer L Raymond
Journal:  Elife       Date:  2014-04-22       Impact factor: 8.713

10.  Principles of operation of a cerebellar learning circuit.

Authors:  David J Herzfeld; Nathan J Hall; Marios Tringides; Stephen G Lisberger
Journal:  Elife       Date:  2020-04-30       Impact factor: 8.140

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