Literature DB >> 3583934

Strial dysfunction in mice with cochleo-saccular abnormalities.

K P Steel, C Barkway, G R Bock.   

Abstract

Most viable dominant spotting (Wv/Wv) mutant mice, which show cochleo-saccular degeneration, were found to have an endocochlear potential (EP) around zero together with a structurally abnormal stria vascularis. Inner hair cells were well preserved, but outer hair cells in the basal half of the cochlea were degenerating, possibly as a result of primary strial dysfunction. Thresholds for the detection of a compound action potential were raised to around 100 dB SPL in the mutants with no EP, and there was little if any cochlear microphonic at the round window. Of the 20 Wv/Wv mice studied, five partially escaped the effects of the mutation and had measurable positive potentials (15-86 mV) in scala media in the basal turn; responses in these animals were intermediate between control responses and those of mutants with no EP. These findings confirm that the pathological processes in this mutant, with cochleo-saccular abnormalities, are fundamentally different from the pathological processes in animals with neuroepithelial abnormalities reported previously [see Steel and Bock (1983) Arch. Otolaryngol. 109, 22-29, for references].

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Year:  1987        PMID: 3583934     DOI: 10.1016/0378-5955(87)90022-0

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  22 in total

1.  Heritability and segregation analysis of deafness in U.S. Dalmatians.

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2.  Endocochlear potential generation is associated with intercellular communication in the stria vascularis: structural analysis in the viable dominant spotting mouse mutant.

Authors:  L Carlisle; K Steel; A Forge
Journal:  Cell Tissue Res       Date:  1990-11       Impact factor: 5.249

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4.  Adaptation of Cochlear Amplification to Low Endocochlear Potential.

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Journal:  Biophys J       Date:  2019-03-30       Impact factor: 4.033

5.  Auditory brainstem response thresholds in a mouse mutant with selective outer hair cell loss.

Authors:  A Schrott; K Stephan; H Spoendlin
Journal:  Eur Arch Otorhinolaryngol       Date:  1990       Impact factor: 2.503

6.  Hearing dysfunction in heterozygous Mitf(Mi-wh) /+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome.

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Review 7.  Application of Mouse Models to Research in Hearing and Balance.

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Journal:  J Assoc Res Otolaryngol       Date:  2016-10-17

8.  A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment.

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Review 9.  Mechanisms and genes in human strial presbycusis from animal models.

Authors:  Kevin K Ohlemiller
Journal:  Brain Res       Date:  2009-03-12       Impact factor: 3.252

10.  Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall.

Authors:  Ying-Peng Liu; Hong-Bo Zhao
Journal:  Cell Tissue Res       Date:  2008-06-26       Impact factor: 5.249

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