Neurobiology of Aging
Volume 32, Issue 9 , Pages 1716-1724, September 2011

F1 (CBA×C57) mice show superior hearing in old age relative to their parental strains: Hybrid vigor or a new animal model for “Golden Ears”?

  • Robert D. Frisina

      Affiliations

    • Department of Otolaryngology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • Department of Neurobiology & Anatomy and Biomedical Engineering, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • International Center for Hearing & Speech Research – National Technical Institute for Deaf, Rochester Inst. Technology, Rochester, NY 14623, USA
    • Corresponding Author InformationCorresponding author at: Otolaryngology Dept., Univ. Rochester Medical School, 601 Elmwood Avenue, Rochester, NY 14642-8629, USA. Tel.: +1 585 275 8130; fax: +1 585 271 8552.
  • ,
  • Ameet Singh

      Affiliations

    • Department of Otolaryngology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • International Center for Hearing & Speech Research – National Technical Institute for Deaf, Rochester Inst. Technology, Rochester, NY 14623, USA
  • ,
  • Matthew Bak

      Affiliations

    • Department of Otolaryngology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • International Center for Hearing & Speech Research – National Technical Institute for Deaf, Rochester Inst. Technology, Rochester, NY 14623, USA
  • ,
  • Sara Bozorg

      Affiliations

    • Department of Otolaryngology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • International Center for Hearing & Speech Research – National Technical Institute for Deaf, Rochester Inst. Technology, Rochester, NY 14623, USA
  • ,
  • Rahul Seth

      Affiliations

    • Department of Otolaryngology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • International Center for Hearing & Speech Research – National Technical Institute for Deaf, Rochester Inst. Technology, Rochester, NY 14623, USA
  • ,
  • Xiaoxia Zhu

      Affiliations

    • Department of Otolaryngology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    • International Center for Hearing & Speech Research – National Technical Institute for Deaf, Rochester Inst. Technology, Rochester, NY 14623, USA

Received 24 June 2009; received in revised form 17 September 2009; accepted 27 September 2009. published online 30 October 2009.

Abstract 

Age-related hearing loss – presbycusis – is the most common communication problem and third most prevalent chronic medical disorder of the aged. The CBA and C57BL/6 mouse strains are useful for studying features of presbycusis. The CBA loses its hearing slowly, like most humans. Because the C57 develops a rapid, high frequency hearing loss by middle age, it has an “old” ear but a relatively young brain, a model that helps separate peripheral (cochlear) from central (brain) etiologies. This field of sensory neuroscience lacks a good mouse model for the 5–10% of aged humans with normal cochlear sensitivity, but who have trouble perceiving speech in background noise. We hypothesized that F1 (CBA×C57) hybrids would have better hearing than either parental strain. Measurements of peripheral auditory sensitivity supported this hypothesis, however, a rapid decline in the auditory efferent feedback system, did not. Therefore, F1s might be an optimal model for studying cases where the peripheral hearing is quite good in old age; thereby allowing isolation of central auditory changes due to brain neurodegeneration.

Keywords: Presbycusis, Aging, Hearing loss, Deafness, Mouse, Cochlea, Central auditory system, Efferent feedback system, Olivocochlear bundle, Neurophysiology

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 Grant Support: NIH Grant P01 AG09524 from the National Institute on Aging, and NIH Grant P30 DC05409 from the National Institute on Deafness & Communication Disorders.

PII: S0197-4580(09)00315-7

doi:10.1016/j.neurobiolaging.2009.09.009

Neurobiology of Aging
Volume 32, Issue 9 , Pages 1716-1724, September 2011