Literature DB >> 6335102

Single unit activity in the nucleus of the basal optic root (nBOR) during optokinetic, vestibular and visuo-vestibular stimulations in the alert pigeon (Columbia livia).

H Gioanni, J Rey, J Villalobos, A Dalbera.   

Abstract

Extracellular recordings were performed in the nucleus of the basal optic root (nBOR) of alert pigeons during optokinetic nystagmus (OKN), vestibulo-ocular reflex (VOR) and combined visuo-vestibular stimulation. Cell identification was assessed either by histological control or by electrophysiological testing (antidromic response to vestibulo-cerebellar or oculomotor complex stimulation). 1) OKN was induced in 8 directions by a binocular stimulation. During the fast phase of OKN, optokinetic after nystagmus (OKAN) or reversed OKAN, most cells showed an inhibition which varied in magnitude independent of the direction of stimulation. A few cells however showed a phasic discharge for some OKN directions. 2) During the slow phase of OKN induced by a binocular stimulation, cells displayed either a tonic activation or a more or less strong inhibition according to the direction of the OKN. Cells were classified in 4 groups, according to their degree of directional specificity. The best OKN direction (slow phase) for maximal cell activation was upwards and naso-upwards, and next to best, naso-temporal and downwards. Maximal cell inhibition occurred during downward, and for some cells during upward, directions. 3) During OKN induced by stimulating the eye contralateral to the recorded nBOR, cell responses resembled those obtained during binocular stimulation, but, during ipsilaterally induced OKN, the cells lost their directional specificity. As a result of binocular integration, neuronal activation seems to originate from contralateral input whereas cell inhibition would mainly come from ipsilateral input. 4) During sinusoidal optokinetic stimulation induced in the temporo downward-naso upward axis, cells showed a more or less marked modulation (according to their directional selectivity) that was closely in phase with the stimulation velocity, and therefore probably with retinal slip. 5) nBOR cells appeared generally unaffected during both the slow phase and the fast phase of the VOR. However, some cells showed a slight but irregular modulation which might imply a weak vestibular input. During visuo-vestibular stimulation, the response resembled that obtained with sinusoidal optokinetic stimulation but the fast phase inhibition was often strengthened in the downwards direction (fast phase).

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Year:  1984        PMID: 6335102     DOI: 10.1007/bf00231131

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


  29 in total

1.  Some visual and other connections to the cerebellum of the pigeon.

Authors:  P G Clarke
Journal:  J Comp Neurol       Date:  1977-08-01       Impact factor: 3.215

2.  Specific projection of displaced retinal ganglion cells upon the accessory optic system in the pigeon (Columbia livia).

Authors:  J H Karten; K V Fite; N Brecha
Journal:  Proc Natl Acad Sci U S A       Date:  1977-04       Impact factor: 11.205

3.  Receptive fields in the accessory optic system of the rabbit.

Authors:  R E Walley
Journal:  Exp Neurol       Date:  1967-01       Impact factor: 5.330

4.  Efferent projections of the visual Wulst upon the nucleus of the basal optic root in the pigeon.

Authors:  J P Rio; J Villalobos; D Miceli; J Repérant
Journal:  Brain Res       Date:  1983-07-18       Impact factor: 3.252

5.  The accessory optic system in the newt, Triturus cristatus: unitary response properties from the basal optic neuropil.

Authors:  G Manteuffel
Journal:  Brain Behav Evol       Date:  1982       Impact factor: 1.808

6.  Electrophysiology of medial terminal nucleus of accessory optic system in the cat.

Authors:  K L Grasse; M S Cynader
Journal:  J Neurophysiol       Date:  1982-08       Impact factor: 2.714

7.  The vestibular nuclei in the domestic hen (Gallus domesticus).

Authors:  J E Wold
Journal:  Exp Brain Res       Date:  1979-01-15       Impact factor: 1.972

8.  Unit activity in accessory optic system in alert monkeys.

Authors:  G Westheimer; S M Blair
Journal:  Invest Ophthalmol       Date:  1974-07

9.  Optokinetic nystagmus in the pigeon (Columba livia). III. Role of the nucleus ectomamillaris (nEM): interactions in the accessory optic system (AOS).

Authors:  H Gioanni; J Villalobos; J Rey; A Dalbera
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

10.  A quantitative analysis of the direction-specific response of Neurons in the cat's nucleus of the optic tract.

Authors:  K P Hoffmann; A Schoppmann
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

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  10 in total

1.  Unilateral pretectal microinjections of SR 95,531, a GABA A antagonist: effects on directional asymmetry of frog monocular OKN.

Authors:  Y H Yücel; B Jardon; N Bonaventure
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

2.  Role of the nucleus geniculatus lateralis ventralis (GLv) in the optokinetic reflex: a lesion study in the pigeon.

Authors:  H Gioanni; A Palacios; A Sansonetti; F Varela
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  The visual response properties of neurons in the nucleus of the basal optic root of the pigeon: a quantitative analysis.

Authors:  D R Wylie; B J Frost
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

4.  Stabilizing gaze reflexes in the pigeon (Columba livia). I. Horizontal and vertical optokinetic eye (OKN) and head (OCR) reflexes.

Authors:  H Gioanni
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

5.  A putative suprachiasmatic nucleus of birds responds to visual motion.

Authors:  J Wallman; C J Saldanha; R Silver
Journal:  J Comp Physiol A       Date:  1994-03       Impact factor: 1.836

6.  Effects on the chicken monocular OKN of unilateral microinjections of GABAA antagonist into the mesencephalic structures responsible for OKN.

Authors:  N Bonaventure; M S Kim; B Jardon
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

7.  Functional activity in the accessory optic system during visual, vestibular and visual-vestibular stimulation in the pigeon.

Authors:  L Telford; B J Frost
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

Review 8.  Visual-Cerebellar Pathways and Their Roles in the Control of Avian Flight.

Authors:  Douglas R Wylie; Cristián Gutiérrez-Ibáñez; Andrea H Gaede; Douglas L Altshuler; Andrew N Iwaniuk
Journal:  Front Neurosci       Date:  2018-04-09       Impact factor: 4.677

9.  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

Review 10.  Integrating brain, behavior, and phylogeny to understand the evolution of sensory systems in birds.

Authors:  Douglas R Wylie; Cristian Gutiérrez-Ibáñez; Andrew N Iwaniuk
Journal:  Front Neurosci       Date:  2015-08-11       Impact factor: 4.677

  10 in total

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