4.5 Article

Age-related central gain with degraded neural synchrony in the auditory brainstem of mice and humans

Journal

NEUROBIOLOGY OF AGING
Volume 115, Issue -, Pages 50-59

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2022.03.014

Keywords

Aging; Central gain; Auditory nerve; Auditory midbrain; Neural synchrony

Funding

  1. National Institute on Deafness and Other Communication Disorders (NIDCD) of the National Institutes of Health (NIH) [R01 DC 014467, R01 DC 017619, P50 DC 0 0 0422, K18 DC018517, T32 DC 014435]
  2. SFARI Pilot Award [649452]
  3. South Carolina Clinical and Translational Research (SCTR) Institute with an academic home at the Medical University of South Carolina
  4. NIH
  5. NCRR [UL1 RR 029882]
  6. National Center for Research Resources, NIH [C06 RR 014516]

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Aging is associated with increased central gain in the auditory midbrain, but without improvements in inter-trial synchrony. Older mice and humans show greater deficits in AN response amplitudes compared to midbrain responses. These results suggest that persistent decreases in synchrony may contribute to auditory processing deficits in older individuals.
Aging is associated with auditory nerve (AN) functional deficits and decreased inhibition in the central auditory system, amplifying central responses in a process referred to here as central gain. Although central gain increases response amplitudes, central gain may not restore disrupted response timing. In this translational study, we measured responses putatively generated by the AN and auditory midbrain in younger and older mice and humans. We hypothesized that older mice and humans exhibit increased central gain without an improvement in inter-trial synchrony in the midbrain. Our data demonstrated greater age-related deficits in AN response amplitudes than auditory midbrain response amplitudes, as shown by significant interactions between inferred neural generator and age group, indicating increased central gain in auditory midbrain. However, synchrony decreases with age in both the AN and midbrain responses. These results reveal age-related increases in central gain without concomitant improvements in synchrony, consistent with those predictions based on decreases in inhibition. Persistent decreases in synchrony may contribute to auditory processing deficits in older mice and humans. Published by Elsevier Inc.

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