Literature DB >> 2358040

Nature of optokinetic response and zonal organization of climbing fiber afferents in the vestibulocerebellum of the pigmented rabbit. I. The flocculus.

M Kusunoki1, M Kano, M S Kano, K Maekawa.   

Abstract

In pigmented rabbits anesthetized with N2O (70%) and halothane (2-4%), Purkinje cells were extracellularly recorded in the flocculus. A large central visual field (60 degrees x 60 degrees) was used to optokinetically stimulate either the ipsi- or contralateral eye, and the direction and velocity selectivities of complex spike responses were examined. For optokinetic stimulation (OKS) delivered to the ipsilateral eye (n = 129), the preferred direction was forward (F, n = 57) or upward (U, n = 37), while the remaining cells (n = 35) showed no response (N). For OKS delivered to the contralateral eye (n = 107), the preferred direction was backward (B, n = 11), downward (D, n = 42) or upward (U, n = 2), and the rest (n = 52) showed N. Cells tested with both eyes (n = 89) fell into five categories based on the preferred direction to ipsi- and contralateral OKS: (1) ipsi-F and contra-B (F/B type, n = 9), (2) ipsi-F but contra-N (F/N type, n = 28), (3) ipsi-U and contra-D (U/D type, n = 13), (4) ipsi-U but contra-N (U/N type, n = 17), and (5) ipsi-N but contra-D (N/D type, n = 22). The optimum velocity was within 0.1-2.0 degrees/s for all cells. On the average, the best response was obtained at 0.2-0.5 degrees/s stimulation. All ipsi-F cells responded to electrical stimulation of the optic tract (OT), while most cells preferring ipsi-U, contra-B and contra-D directions did not respond. No characteristic feature was found in cells innervated with collateralized climbing fiber branches to the nodulus. In the flocculus, cells preferring horizontal orientation (H cells, preferring ipsi-F and/or contra-B directions) were localized in a narrow dorsoventral zone (less than 1.0 mm) along the caudal border of the rostral one third, while those preferring the vertical orientation (V cells, preferring ipsi-U and/or contra-D directions) were in two distinct narrow zones located rostral and caudal to the H cell zone. H and V cells were intermingled in the central portion of the ventral flocculus. These four zones are in good agreement with previously defined H, anterior V, posterior V and R zones, respectively. The results indicate that the subdivision of the flocculus which controls horizontal (vertical) eye movements receives information regarding movements of the visual surround in the horizontal (vertical) orientation through visual climbing fiber afferents, thus being organized in olivo-cortico-nuclear functional units for control of eye movements.

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Year:  1990        PMID: 2358040     DOI: 10.1007/bf00228151

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  40 in total

1.  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

2.  Impulse discharges from flocculus Purkinje cells of alert rabbits during visual stimulation combined with horizontal head rotation.

Authors:  B Ghelarducci; M Ito; N Yagi
Journal:  Brain Res       Date:  1975-04-04       Impact factor: 3.252

3.  Spatial organization of visual messages of the rabbit's cerebellar flocculus. I. Typology of inferior olive neurons of the dorsal cap of Kooy.

Authors:  C S Leonard; J I Simpson; W Graf
Journal:  J Neurophysiol       Date:  1988-12       Impact factor: 2.714

4.  The projection of the "vestibulocerebellum" onto the vestibular nuclei in the cat.

Authors:  P Angaut; A Brodal
Journal:  Arch Ital Biol       Date:  1967-11       Impact factor: 1.000

5.  Specific patterns of neuronal connexions involved in the control of the rabbit's vestibulo-ocular reflexes by the cerebellar flocculus.

Authors:  M Ito; N Nisimaru; M Yamamoto
Journal:  J Physiol       Date:  1977-03       Impact factor: 5.182

6.  Effects of vestibulocerebellar lesions upon dynamic characteristics and adaptation of vestibulo-ocular and optokinetic responses in pigmented rabbits.

Authors:  S Nagao
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

7.  Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells.

Authors:  M Ito; M Sakurai; P Tongroach
Journal:  J Physiol       Date:  1982-03       Impact factor: 5.182

8.  Eye velocity responsiveness and its proprioceptive component in the floccular Purkinje cells of the alert pigmented rabbit.

Authors:  Y Miyashita
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

9.  Bilateral visual inputs to the dorsal cap of inferior olive: differential localization and inhibitory interactions.

Authors:  T Takeda; K Maekawa
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

10.  Topographical representation in rabbit cerebellar flocculus for various afferent inputs from the brainstem investigated by means of retrograde axonal transport of horseradish peroxidase.

Authors:  M Yamamoto
Journal:  Neurosci Lett       Date:  1979-04       Impact factor: 3.046

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  10 in total

1.  Purkinje cells in the vestibulocerebellum of the pigeon respond best to either translational or rotational wholefield visual motion.

Authors:  D R Wylie; B J Frost
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

2.  Directional organization of eye movement and visual signals in the floccular lobe of the monkey cerebellum.

Authors:  R J Krauzlis; S G Lisberger
Journal:  Exp Brain Res       Date:  1996-05       Impact factor: 1.972

3.  Crossing zones in the vestibulocerebellum: a commentary.

Authors:  John I Simpson
Journal:  Cerebellum       Date:  2011-09       Impact factor: 3.847

4.  Nature of optokinetic response and zonal organization of climbing fiber afferents in the vestibulocerebellum of the pigmented rabbit. II. The nodulus.

Authors:  M Kano; M S Kano; M Kusunoki; K Maekawa
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

5.  Cerebellar encoding of multiple candidate error cues in the service of motor learning.

Authors:  Christine C Guo; Michael C Ke; Jennifer L Raymond
Journal:  J Neurosci       Date:  2014-07-23       Impact factor: 6.167

6.  Optokinetic response of simple spikes of Purkinje cells in the cerebellar flocculus and nodulus of the pigmented rabbit.

Authors:  M Kano; M S Kano; K Maekawa
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

7.  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

8.  Receptive field organization of climbing fiber afferents responding to optokinetic stimulation in the cerebellar nodulus and flocculus of the pigmented rabbit.

Authors:  M S Kano; M Kano; K Maekawa
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

9.  Optokinetic response of cells in the nucleus reticularis tegmenti pontis of the pigmented rabbit.

Authors:  M Kano; K Iino; K Maekawa; M S Kano
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

10.  Processing of visual signals related to self-motion in the cerebellum of pigeons.

Authors:  Douglas R Wylie
Journal:  Front Behav Neurosci       Date:  2013-02-12       Impact factor: 3.558

  10 in total

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