Literature DB >> 8884385

Development of vestibular and auditory function: effects of hypothyroidism and thyroxine replacement therapy on nystagmus and auditory evoked potentials in the pigmented rat.

G Meza1, D Acuña, C Escobar.   

Abstract

The functional development of semicircular canals and some brainstem structures of the auditory system was followed in parallel with time in control and propylthiouracyl-induced hypothyroid pigmented rats by respective recording of postrotatory nystagmus response and auditory evoked brainstem potentials, with the aim of discovering the timing of permanent alterations of these responses in congenital hypothyroidism. A group of hypothyroid rats which under went thyroxine-replacement therapy from postnatal day 12 onward was also included in our studies to corroborate the involvement of thyroid hormones in these effects. Postrotatory nystagmus and auditory evoked responses were absent in congenital hypothyroid rats. In the thyroxine-replaced group postrotatory nystagmus values showed no differences from the control group from postnatal day 28 onward. Auditory evoked potentials in thyroxine-replaced animals could not be elicited at 30 dB, but by increasing the intensity of stimulus to 70 dB, values of latencies of the four waves composing the response were indistinguishable from controls from postnatal day 39 and thereafter. These results show that hypothyroidism affects both semicircular canal and auditory function, the latter more severely than the former, but that these effects can be prevented when thyroxine replacement treatment is started in early stages of postnatal development.

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Year:  1996        PMID: 8884385     DOI: 10.1016/0736-5748(95)00100-x

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  5 in total

1.  Thyroid hormone receptor alpha1 is a critical regulator for the expression of ion channels during final differentiation of outer hair cells.

Authors:  Harald Winter; Claudia Braig; Ulrike Zimmermann; Jutta Engel; Karin Rohbock; Marlies Knipper
Journal:  Histochem Cell Biol       Date:  2007-05-23       Impact factor: 4.304

2.  Complete activation of thyroid hormone receptor β by T3 is essential for normal cochlear function and morphology in mice.

Authors:  Claus-Peter Richter; Adrian Münscher; Danielle Santana Machado; Fredric E Wondisford; Tania M Ortiga-Carvalho
Journal:  Cell Physiol Biochem       Date:  2011-12-15

3.  TBL1Y: a new gene involved in syndromic hearing loss.

Authors:  Mariateresa Di Stazio; Chiara Collesi; Diego Vozzi; Wei Liu; Mike Myers; Anna Morgan; Pio Adamo D Adamo; Giorgia Girotto; Elisa Rubinato; Mauro Giacca; Paolo Gasparini
Journal:  Eur J Hum Genet       Date:  2018-10-19       Impact factor: 4.246

4.  The role of thyroid and parathyroid metabolism disorders in the etiology of sudden onset dizziness.

Authors:  Ugur Lok; Sinan Hatipoglu; Umut Gulacti; Abdullah Arpaci; Nurettin Aktas; Tayfun Borta
Journal:  Med Sci Monit       Date:  2014-12-16

5.  Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.

Authors:  I Jill Karolyi; Gary A Dootz; Karin Halsey; Lisa Beyer; Frank J Probst; Kenneth R Johnson; Albert F Parlow; Yehoash Raphael; David F Dolan; Sally A Camper
Journal:  Mamm Genome       Date:  2007-09-22       Impact factor: 3.224

  5 in total

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