Short-term NAD+ supplementation prevents hearing loss in mouse models of Cockayne syndrome

Research output: Contribution to journalJournal articleResearchpeer-review

  • Mustafa N Okur
  • Beatrice Mao
  • Risako Kimura
  • Scott Haraczy
  • Tracy Fitzgerald
  • Kamren Edwards-Hollingsworth
  • Jane Tian
  • Wasif Osmani
  • Deborah L Croteau
  • Matthew W Kelley
  • Bohr, Vilhelm

Age-related hearing loss (ARHL) is one of the most common disorders affecting elderly individuals. There is an urgent need for effective preventive measures for ARHL because none are currently available. Cockayne syndrome (CS) is a premature aging disease that presents with progressive hearing loss at a young age, but is otherwise similar to ARHL. There are two human genetic complementation groups of CS, A and B. While the clinical phenotypes in patients are similar, the proteins have very diverse functions, and insight into their convergence is of great interest. Here, we use mouse models for CS (CSA-/- and CSB m/m ) that recapitulate the hearing loss in human CS patients. We previously showed that NAD+, a key metabolite with various essential functions, is reduced in CS and associated with multiple CS phenotypes. In this study, we report that NAD+ levels are reduced in the cochlea of CSB m/m mice and that short-term treatment (10 days) with the NAD+ precursor nicotinamide riboside (NR), prevents hearing loss, restores outer hair cell loss, and improves cochlear health in CSB m/m mice. Similar, but more modest effects were observed in CSA-/- mice. Remarkably, we observed a reduction in synaptic ribbon counts in the presynaptic zones of inner hair cells in both CSA -/- and CSB m/m mice, pointing to a converging mechanism for cochlear defects in CS. Ribbon synapses facilitate rapid and sustained synaptic transmission over long periods of time. Ribeye, a core protein of synaptic ribbons, possesses an NAD(H) binding pocket which regulates its activity. Intriguingly, NAD+ supplementation rescues reduced synaptic ribbon formation in both CSA -/- and CSB m/m mutant cochleae. These findings provide valuable insight into the mechanism of CS- and ARHL-associated hearing loss, and suggest a possible intervention.

Original languageEnglish
Article number1
Journalnpj Aging and Mechanisms of Disease
Volume6
Number of pages10
ISSN2056-3973
DOIs
Publication statusPublished - Jan 2020

ID: 257866420