Literature DB >> 8951429

Direct effects of intraperilymphatic reactive oxygen species generation on cochlear function.

W J Clerici1, L Yang.   

Abstract

Reactive oxygen species (ROS) generation may play a role in ototoxicity, however, the specific effects of ROS generation upon cochlear function are unstudied. Therefore, guinea pig cochleas were instilled with artificial perilymph (AP), H2O2, or confirmed generating systems for the superoxide anion (O2-) or the hydroxyl radical (OH.), or with an ROS system plus its respective scavenger -catalase (CAT), superoxide dismutase (SOD) or deferoxamine (DEF). O2- generating system instillation led to significantly greater mean high frequency compound action potential (CAP) threshold shifts at 10 and 120 min post infusion than seen in AP control or SOD/O2- groups. H2O2 group CAP threshold shifts were significantly greater than control and CAT/H2O2 group values at 10 (16-30 kHz), and 120 min (above 12 kHz). OH generating system instillation led to significantly greater CAP threshold shifts at 10 (12-30 kHz) and 120 min (above 6 kHz) than seen in control or DEF/OH groups. No significant CAP differences were found between controls and scavenger/ROS groups. Mean 1.0 microV cochlear microphonic isopotential curve shift values did not systematically differ among groups. The rapid degradation of high frequency CAP threshold sensitivity seen here may provide insight into the portion of cochlear dysfunction which is ROS-mediated following noise, radiation or chemical exposures.

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Year:  1996        PMID: 8951429     DOI: 10.1016/s0378-5955(96)00126-8

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


  24 in total

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Journal:  J Neurosci       Date:  2010-03-03       Impact factor: 6.167

2.  Vitamins A, C, and E and selenium in the treatment of idiopathic sudden sensorineural hearing loss.

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Journal:  Eur Arch Otorhinolaryngol       Date:  2014-02-12       Impact factor: 2.503

3.  Damage and threshold shift resulting from cochlear exposure to paraquat-generated superoxide.

Authors:  Eric C Bielefeld; Bo Hua Hu; Kelly Carney Harris; Donald Henderson
Journal:  Hear Res       Date:  2005-09       Impact factor: 3.208

4.  Adenosine and the auditory system.

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Journal:  Curr Neuropharmacol       Date:  2009-09       Impact factor: 7.363

5.  Selective vulnerability of the cochlear Basal turn to acrylonitrile and noise.

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Review 6.  A comprehensive study of oxidative stress in sudden hearing loss.

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Journal:  Eur Arch Otorhinolaryngol       Date:  2016-09-10       Impact factor: 2.503

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Journal:  Eur Arch Otorhinolaryngol       Date:  2004-05-28       Impact factor: 2.503

Review 8.  Cisplatin ototoxicity and protection: clinical and experimental studies.

Authors:  Leonard P Rybak; Debashree Mukherjea; Sarvesh Jajoo; Vickram Ramkumar
Journal:  Tohoku J Exp Med       Date:  2009-11       Impact factor: 1.848

9.  Assessment of nutrient supplement to reduce gentamicin-induced ototoxicity.

Authors:  C G Le Prell; C Ojano-Dirain; E W Rudnick; M A Nelson; S J DeRemer; D M Prieskorn; J M Miller
Journal:  J Assoc Res Otolaryngol       Date:  2014-03-04

Review 10.  siRNA-mediated knock-down of NOX3: therapy for hearing loss?

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Journal:  Cell Mol Life Sci       Date:  2012-05-05       Impact factor: 9.261

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