Literature DB >> 15492889

Posture, head stability, and orientation recovery during vestibular regeneration in pigeons.

J David Dickman1, Insook Lim.   

Abstract

Compensatory behavior such as oculomotor, gaze, and postural responses that occur during movement largely depend upon a functioning vestibular system. In the present study, the initial loss and subsequent recovery of postural and head stability in pigeons undergoing vestibular regeneration were examined. Adult pigeons were trained to manipulate a straight run chamber to peck an illuminated key for fluid reward. Six behavioral measures assessing performance, posture, and head stability were quantified. These included run latency, steps (walking), path negotiation (lane changes), gaze saccades, head bobs, and head shakes. Once normative values were obtained for four birds, complete lesion of all receptor cells and denervation of the epithelia in the vestibular endorgans were produced using a single intralabyrinthine application of streptomycin sulfate. Each bird was then tested at specific times during regeneration and the same behavioral measures examined. At 7 days post-streptomycin treatment (PST), all birds exhibited severe postural and head instability, with tremors, head shakes, staggering, and circling predominating. No normal trial runs, walking, gaze saccades, or head bobs were present. Many of these dysfunctions persisted through 3-4 weeks PST. Gradually, tremor and head shakes diminished and were replaced with an increasing number of normal head bobs during steps and gaze saccades. Beginning at 4 weeks PST, but largely inaccurate, was the observed initiation of directed steps, less staggering, and some successful path negotiation. As regeneration progressed, spatial orientation and navigation ability increased and, by 49 days PST, most trials were successful. By 70 days PST, all birds had recovered to pretreatment levels. Thus, it was observed that ataxia must subside, coincident with normalized head and postural stability prior to the recovery of spatial orientation and path navigation recovery. Parallels in recovery were drawn to hair cell regeneration and afferent responsiveness, as inferred from present results and those in other investigations.

Entities:  

Keywords:  NASA Discipline Neuroscience; Non-NASA Center

Mesh:

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Year:  2004        PMID: 15492889      PMCID: PMC2504555          DOI: 10.1007/s10162-004-4047-0

Source DB:  PubMed          Journal:  J Assoc Res Otolaryngol        ISSN: 1438-7573


  59 in total

1.  Hair cell and supporting cell density and distribution in the normal and regenerating posterior crista ampullaris of the pigeon.

Authors:  G A Kevetter; K R Blumberg; M J Correia
Journal:  Int J Dev Neurosci       Date:  2000-12       Impact factor: 2.457

2.  Hair cell recovery in mitotically blocked cultures of the bullfrog saccule.

Authors:  R A Baird; M D Burton; A Lysakowski; D S Fashena; R A Naeger
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

3.  Three-dimensional organization of vestibular related eye movements to rotational motion in pigeons.

Authors:  J D Dickman; M Beyer; B J Hess
Journal:  Vision Res       Date:  2000       Impact factor: 1.886

4.  Functional recovery of anterior semicircular canal afferents following hair cell regeneration in birds.

Authors:  Richard Boyle; Stephen M Highstein; John P Carey; Jinping Xu
Journal:  J Assoc Res Otolaryngol       Date:  2002-06

5.  Hippocampal spatial representations require vestibular input.

Authors:  Robert W Stackman; Ann S Clark; Jeffrey S Taube
Journal:  Hippocampus       Date:  2002       Impact factor: 3.899

6.  Afferent innervation patterns of the saccule in pigeons.

Authors:  M Zakir; D Huss; J D Dickman
Journal:  J Neurophysiol       Date:  2003-01       Impact factor: 2.714

7.  Three-dimensional organization of vestibular-related eye movements to off-vertical axis rotation and linear translation in pigeons.

Authors:  J D Dickman; D E Angelaki
Journal:  Exp Brain Res       Date:  1999-12       Impact factor: 1.972

8.  Rats with lesions of the vestibular system require a visual landmark for spatial navigation.

Authors:  Robert W Stackman; Aaron M Herbert
Journal:  Behav Brain Res       Date:  2002-01-07       Impact factor: 3.332

9.  Visual influences on the development and recovery of the vestibuloocular reflex in the chicken.

Authors:  C T Goode; D L Maney; E W Rubel; A F Fuchs
Journal:  J Neurophysiol       Date:  2001-03       Impact factor: 2.714

10.  Inputs from regularly and irregularly discharging vestibular nerve afferents to secondary neurons in squirrel monkey vestibular nuclei. III. Correlation with vestibulospinal and vestibuloocular output pathways.

Authors:  R Boyle; J M Goldberg; S M Highstein
Journal:  J Neurophysiol       Date:  1992-08       Impact factor: 2.714

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  4 in total

1.  Regeneration of vestibular horizontal semicircular canal afferents in pigeons.

Authors:  Asim Haque; Mridha Zakir; J David Dickman
Journal:  J Neurophysiol       Date:  2009-06-10       Impact factor: 2.714

Review 2.  Development and regeneration of vestibular hair cells in mammals.

Authors:  Joseph C Burns; Jennifer S Stone
Journal:  Semin Cell Dev Biol       Date:  2016-11-15       Impact factor: 7.727

Review 3.  A brief history of hair cell regeneration research and speculations on the future.

Authors:  Edwin W Rubel; Stephanie A Furrer; Jennifer S Stone
Journal:  Hear Res       Date:  2013-01-12       Impact factor: 3.208

4.  Partial Aminoglycoside Lesions in Vestibular Epithelia Reveal Broad Sensory Dysfunction Associated with Modest Hair Cell Loss and Afferent Calyx Retraction.

Authors:  David R Sultemeier; Larry F Hoffman
Journal:  Front Cell Neurosci       Date:  2017-10-27       Impact factor: 5.505

  4 in total

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