Literature DB >> 12657453

Hypothyroidism prevents developmental neuronal loss during auditory organ development.

Joaquin Rueda1, Jorge J Prieto, Raquel Cantos, María L Sala, Jaime A Merchán.   

Abstract

The deficit of thyroid hormone leads to several structural and physiological modifications in the auditory receptor: the outer hair cells present an immature morphology, abnormal persistence of the afferent dendrites and incomplete development of the efferent terminals. The aim of this work was to perform a quantitative and morphometric study of the spiral ganglion neurons in control and hypothyroid animals. The cochleae from both experimental groups were processed in order to obtain plastic sections. In control animals the size of the neurons increased throughout development and was larger in the basal than in the apical portion of the cochlea. In hypothyroid animals, the cell death that takes place normally during development did not occur, and there was no differentiation into types I and II neurons. The size of the neurons also increased with development in treated animals, but they were smaller than in control animals, and in this case the neurons in the apex were larger than in the base. This study shows that hypothyroidism alters the normal development of the spiral ganglion neurons.

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Year:  2003        PMID: 12657453     DOI: 10.1016/s0168-0102(03)00009-9

Source DB:  PubMed          Journal:  Neurosci Res        ISSN: 0168-0102            Impact factor:   3.304


  7 in total

1.  Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.

Authors:  Mirna Mustapha; Qing Fang; Tzy-Wen Gong; David F Dolan; Yehoash Raphael; Sally A Camper; R Keith Duncan
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

2.  Thyroid hormone is required for pruning, functioning and long-term maintenance of afferent inner hair cell synapses.

Authors:  Srividya Sundaresan; Jee-Hyun Kong; Qing Fang; Felipe T Salles; Felix Wangsawihardja; Anthony J Ricci; Mirna Mustapha
Journal:  Eur J Neurosci       Date:  2015-10-28       Impact factor: 3.386

3.  Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression.

Authors:  Philine Wangemann; Hyoung-Mi Kim; Sara Billings; Kazuhiro Nakaya; Xiangming Li; Ruchira Singh; David S Sharlin; Douglas Forrest; Daniel C Marcus; Peying Fong
Journal:  Am J Physiol Renal Physiol       Date:  2009-08-19

4.  Thyroid hormone is required for the pruning of afferent type II spiral ganglion neurons in the mouse cochlea.

Authors:  S Sundaresan; S Balasubbu; M Mustapha
Journal:  Neuroscience       Date:  2015-11-18       Impact factor: 3.590

5.  Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking pendrin expression.

Authors:  Hyoung-Mi Kim; Philine Wangemann
Journal:  PLoS One       Date:  2010-11-17       Impact factor: 3.240

6.  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

7.  A lack of immune system genes causes loss in high frequency hearing but does not disrupt cochlear synapse maturation in mice.

Authors:  Melissa A Calton; Dasom Lee; Srividya Sundaresan; Diana Mendus; Rose Leu; Felix Wangsawihardja; Kenneth R Johnson; Mirna Mustapha
Journal:  PLoS One       Date:  2014-05-07       Impact factor: 3.240

  7 in total

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