Literature DB >> 8600121

Development of endocochlear potential and its negative component in mouse cochlea.

M Sadanaga1, T Morimitsu.   

Abstract

The chronological developmental processes of endocochlear potential (EP) and negative endocochlear potential (-EP) were investigated as a function of age from birth in the basal and second cochlear turns in normal ICR-strain mice. The EP of the basal turn developed between 5 and 17 days after birth (DAB). The -EP of the basal turn attained to its mature level on 11 DAB and it increased its absolute value further between 12 and 16 DAB and then, recovered to its mature level again on 20 DAB. The developmental processes of EP and -EP of the second turn followed similar courses to those of the basal turn although they were several millivolts different on each day in detail. The results suggest that the developmental processes of the +EP and the -EP are different. The time of reaching minimum -EP during anoxia were measured and the rate of EP decline were calculated on each animal. The rate of EP decline increased rapidly on 10 DAB, almost coinciding the day which EP began to increase abruptly. Although the rate of EP decline is influenced by several processes, this result showed one of the possibility that the sensitivity of the stria vascularis to hypoxia may develop parallel to the development of the EP.

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Mesh:

Year:  1995        PMID: 8600121     DOI: 10.1016/0378-5955(95)00133-x

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


  33 in total

1.  Molecular characterization of anion exchangers in the cochlea.

Authors:  U Zimmermann; I Köpschall; K Rohbock; G J Bosman; H P Zenner; M Knipper
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2.  Otoacoustic emissions without somatic motility: can stereocilia mechanics drive the mammalian cochlea?

Authors:  M C Liberman; Jian Zuo; J J Guinan
Journal:  J Acoust Soc Am       Date:  2004-09       Impact factor: 1.840

3.  ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.

Authors:  Oscar Diaz-Horta; Clemer Abad; Levent Sennaroglu; Joseph Foster; Alexandra DeSmidt; Guney Bademci; Suna Tokgoz-Yilmaz; Duygu Duman; F Basak Cengiz; M'hamed Grati; Suat Fitoz; Xue Z Liu; Amjad Farooq; Faiqa Imtiaz; Benjamin B Currall; Cynthia Casson Morton; Michiru Nishita; Yasuhiro Minami; Zhongmin Lu; Katherina Walz; Mustafa Tekin
Journal:  Proc Natl Acad Sci U S A       Date:  2016-05-09       Impact factor: 11.205

4.  Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction.

Authors:  Taku Ito; Xiangming Li; Kiyoto Kurima; Byung Yoon Choi; Philine Wangemann; Andrew J Griffith
Journal:  Neurobiol Dis       Date:  2014-02-19       Impact factor: 5.996

5.  Spontaneous activations follow a common developmental course across primary sensory areas in mouse neocortex.

Authors:  Charles G Frye; Jason N MacLean
Journal:  J Neurophysiol       Date:  2016-05-04       Impact factor: 2.714

Review 6.  Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.

Authors:  Emilie Hoang Dinh; Shoeb Ahmad; Qing Chang; Wenxue Tang; Benjamin Stong; Xi Lin
Journal:  Brain Res       Date:  2009-02-20       Impact factor: 3.252

7.  Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.

Authors:  Martine Cohen-Salmon; Thomas Ott; Vincent Michel; Jean Pierre Hardelin; Isabelle Perfettini; Michel Eybalin; Tao Wu; Daniel C Marcus; Philine Wangemann; Klaus Willecke; Christine Petit
Journal:  Curr Biol       Date:  2002-07-09       Impact factor: 10.834

8.  Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.

Authors:  Ruchira Singh; Philine Wangemann
Journal:  Am J Physiol Renal Physiol       Date:  2007-10-24

9.  The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.

Authors:  Melanie Schütz; Pietro Scimemi; Paromita Majumder; Romolo Daniele De Siati; Giulia Crispino; Laura Rodriguez; Mario Bortolozzi; Rosamaria Santarelli; Anke Seydel; Stephan Sonntag; Neil Ingham; Karen P Steel; Klaus Willecke; Fabio Mammano
Journal:  Hum Mol Genet       Date:  2010-09-21       Impact factor: 6.150

10.  Age-related auditory pathology in the CBA/J mouse.

Authors:  Su-Hua Sha; Ariane Kanicki; Gary Dootz; Andra E Talaska; Karin Halsey; David Dolan; Richard Altschuler; Jochen Schacht
Journal:  Hear Res       Date:  2008-06-07       Impact factor: 3.208

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