Urolithin A prevents age-related hearing loss in C57BL/6J mice likely by inducing mitophagy

Exp Gerontol. 2024 Nov:197:112589. doi: 10.1016/j.exger.2024.112589. Epub 2024 Sep 24.

Abstract

Mitochondrial dysfunction with aging is associated with the development of age-related hearing loss. Mitophagy is a cardinal mechanism to maintain a healthy mitochondrial population through the turnover of damaged mitochondria. Declining mitophagy with age causes a buildup of damaged mitochondria, leading to sensory organ dysfunction. The effect of Urolithin A (UA), a mitophagy inducer, was investigated on age-related hearing loss in a mouse model. C57BL/6J mice were treated with UA from 6 to 10 months of age. UA attenuated an auditory brainstem responses (ABR) threshold shift at 8, 16, and 32 kHz frequencies, and improved mitochondrial DNA integrity and ATP production in the cochlea and auditory cortex. The mRNA levels of mitophagy-related genes and protein levels of PINK1, Parkin, BNIP3, and LC3B increased in the cochlea and auditory cortex. The expression of mitophagosomes and mitophagolysosomes in the cochlea, spiral ganglion, auditory cortex, and inferior colliculus increased, together with the expression of Parkin and BNIP3 in the cochlea, spiral ganglion, auditory cortex, and inferior colliculus. These results indicate that UA counteracted mitophagy decline in the auditory system and prevented age-related hearing loss. UA can be used as a potential agent to prevent age-related hearing loss.

Keywords: Age-related hearing loss; Mitochondria; Mitophagy; Urolithin A.

MeSH terms

  • Aging
  • Animals
  • Auditory Cortex / drug effects
  • Auditory Cortex / metabolism
  • Cochlea / drug effects
  • Cochlea / metabolism
  • Cochlea / pathology
  • Coumarins* / pharmacology
  • DNA, Mitochondrial / metabolism
  • Disease Models, Animal
  • Evoked Potentials, Auditory, Brain Stem* / drug effects
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mitophagy* / drug effects
  • Presbycusis* / metabolism
  • Presbycusis* / pathology
  • Presbycusis* / prevention & control
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • 3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one
  • BNip3 protein, mouse
  • Coumarins
  • DNA, Mitochondrial
  • Membrane Proteins
  • Mitochondrial Proteins
  • parkin protein
  • PTEN-induced putative kinase
  • Ubiquitin-Protein Ligases