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Age-related cochlear hair cell loss is enhanced in mice lacking copper/zinc superoxide dismutase

  • SUNY Buffalo
  • Teva Pharmaceutical Industries Ltd.

Research output: Contribution to journalArticlepeer-review

167 Scopus citations

Abstract

Age-related hearing loss in humans and many strains of mice is associated with a base-to-apex gradient of cochlear hair cell loss. To determine if copper/zinc superoxide dismutase (Cu/Zn SOD) deficiency influences age-related cochlear pathology, we compared hair cell losses in cochleas obtained from 2-, 7-, and 17- to 19-month-old wild type (WT) mice with normal levels of Cu/Zn SOD and mutant knockout (KO) mice with a targeted deletion of Sod1, the gene that codes for Cu/Zn SOD. WT and KO mice exhibited similar patterns of hair cell loss with age, i.e., a baso-apical progression of hair cell loss, with greater loss of outer hair cells than inner hair cells. Within each age group, the magnitude of loss was much greater in KO mice compared to WT mice. The results indicate that Cu/Zn SOD deficiency potentiates cochlear hair cell degeneration, presumably through metabolic pathways involving the superoxide radical. Copyright (C) 1999 Elsevier Science Inc.

Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalNeurobiology of Aging
Volume20
Issue number1
DOIs
StatePublished - 1999

Keywords

  • Age-related hearing loss
  • Antioxidant enzymes
  • Cochlea
  • Genes
  • Knock-out mice
  • presbycusis
  • Reactive oxygen species
  • Superoxide dismutase

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