Literature DB >> 8006858

Morphological and electrophysiological consequences of unilateral pre- versus postganglionic vestibular lesions in the frog.

A W Kunkel1, N Dieringer.   

Abstract

The combined removal of the labyrinthine sense organs and of the ganglion of Scarpa on one side (postganglionic section) resulted in a degeneration of afferent fibres in the eighth nerve of the frog (Rana temporaria) within 2-4 days. If the eighth nerve was sectioned more peripherally (preganglionic section) and its distal part was removed together with the labyrinthine organs degeneration of afferent fibres was absent or restricted to very few fibres. Electrical stimulation of vestibular afferents in vitro evoked monosynaptic field potentials in the ipsilateral and via commissural fibres di- and polysynaptic field potentials in the contralateral vestibular nuclei. Afferent-evoked field potentials recorded on the intact side of chronic frogs (> or = 60 days) with a pre- or postganglionic lesion and afferent-evoked field potentials recorded on the operated side of chronic frogs with a preganglionic lesion had amplitudes that were very similar to those recorded in control frogs. Commissurally evoked field potentials recorded on the operated side of chronic frogs with pre- or postganglionic lesions were significantly increased (by about 90%) with respect to control amplitudes. In both groups the time-course of this increase was very similar, started between 15 and 30 days and saturated for survival periods longer than 60 days. Unilateral inactivation of vestibular afferents, but not degeneration, is the likely common denominator of the central process leading to the reported neural changes. A reactive supersensitivity of central vestibular neurons on the operated side for glutamate as a possible mechanism is unlikely, since converging afferent and commissural inputs are both glutamatergic and only one of them, the commissural input, was potentiated. Comparison of the time-courses of neural changes in the vestibular nuclei and postural recovery in the same individuals excludes a causal relation between both phenomena.

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Year:  1994        PMID: 8006858     DOI: 10.1007/BF00217383

Source DB:  PubMed          Journal:  J Comp Physiol A            Impact factor:   1.836


  38 in total

1.  Mechanisms of compensation for vestibular deficits in the frog. I. Modification of the excitatory commissural system.

Authors:  N Dieringer; W Precht
Journal:  Exp Brain Res       Date:  1979-07-02       Impact factor: 1.972

2.  Modification of synaptic input following unilateral labyrinthectomy.

Authors:  N Dieringer; W Precht
Journal:  Nature       Date:  1977-09-29       Impact factor: 49.962

3.  Quantification of synaptic density changes in the medial vestibular nucleus of the cat following vestibular neurectomy.

Authors:  J Raymond; L Ez-Zaher; D Demêmes; M Lacour
Journal:  Restor Neurol Neurosci       Date:  1991-01-01       Impact factor: 2.406

4.  Crossed effects on central vestibular neurons in the horizontal canal system of the frog.

Authors:  S Ozawa; W Precht; H Shimazu
Journal:  Exp Brain Res       Date:  1974-02-28       Impact factor: 1.972

5.  A reliable and sensitive method to localize terminal degeneration and lysosomes in the central nervous system.

Authors:  F Gallyas; J R Wolff; H Böttcher; L Zaborszky
Journal:  Stain Technol       Date:  1980-09

6.  Spinal compensation for postural deficits after hemilabyrinthectomy?

Authors:  H Straka; A Kunkel; N Dieringer
Journal:  Neuroreport       Date:  1993-09       Impact factor: 1.837

7.  Short- and long-term modifications of vestibulo-ocular response dynamics following unilateral vestibular nerve lesions in the cat.

Authors:  C Maioli; W Precht; S Ried
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

8.  Increased projection of ascending dorsal root fibers to vestibular nuclei after hemilabyrinthectomy in the frog.

Authors:  N Dieringer; H Künzle; W Precht
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

9.  Changes in compensatory eye movements after unilateral labyrinthectomy in the rabbit.

Authors:  E A Baarsma; H Collewijn
Journal:  Arch Otorhinolaryngol       Date:  1975-12-30

10.  Evidence for N-methyl-D-aspartic acid receptor-mediated modulation of the commissural input to central vestibular neurons of the frog.

Authors:  T Knöpfel
Journal:  Brain Res       Date:  1987-11-24       Impact factor: 3.252

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  6 in total

1.  Functional characteristics of the input-output correlation in the vestibular nuclear complex of the frog.

Authors:  V V Fanardzhyan; L R Manvelyan; V L Zakaryan; A M Nasoyan
Journal:  Neurosci Behav Physiol       Date:  2000 Mar-Apr

2.  The frog vestibular system as a model for lesion-induced plasticity: basic neural principles and implications for posture control.

Authors:  François M Lambert; Hans Straka
Journal:  Front Neurol       Date:  2012-04-03       Impact factor: 4.003

3.  Long-Term Balance Outcomes in Vestibular Ablative Surgeries.

Authors:  Fakih Cihat Eravcı; Metin Yılmaz; Ebru Şansal; Nagihan Gülhan; Recep Karamert; Hakan Tutar; Mehmet Birol Uğur
Journal:  Turk Arch Otorhinolaryngol       Date:  2021-03-26

4.  Surgical techniques and functional evaluation for vestibular lesions in the mouse: unilateral labyrinthectomy (UL) and unilateral vestibular neurectomy (UVN).

Authors:  François Simon; David Pericat; Cassandre Djian; Desdemona Fricker; Françoise Denoyelle; Mathieu Beraneck
Journal:  J Neurol       Date:  2020-06-17       Impact factor: 4.849

Review 5.  How Does the Central Nervous System for Posture and Locomotion Cope With Damage-Induced Neural Asymmetry?

Authors:  Didier Le Ray; Mathias Guayasamin
Journal:  Front Syst Neurosci       Date:  2022-03-03

6.  Acute consequences of a unilateral VIIIth nerve transection on vestibulo-ocular and optokinetic reflexes in Xenopus laevis tadpoles.

Authors:  Parthena Soupiadou; Clayton Gordy; Michael Forsthofer; Rosario Sanchez-Gonzalez; Hans Straka
Journal:  J Neurol       Date:  2020-09-11       Impact factor: 4.849

  6 in total

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