# Prevention of Noise-Induced Acceleration of Age-Related Hearing Loss

> **NIH VA I01** · VETERANS HEALTH ADMINISTRATION · 2020 · —

## Abstract

The proposed studies test mechanism-based, clinically relevant interventions to meet the challenges of
aging in the Veteran population. The underlying hypothesis is that prior exposure to noise, such as that
which occurs to service members, contributes to the burden of later age-related hearing loss (ARHL)
resulting in an earlier onset and a greater hearing impairment. Studies use the UM-HET4 model and test a
small arms fire (SAF)-like impulse noise, chosen for military relevance and a 8-16 kHz 100 dB noise,
chosen because it has already been shown to accelerate a component of ARHL in the mouse model. Noise
(or sham) is given at 4 months of age to model noise during service as a young adult. Four distinct
components of ARHL are assessed: 1) loss of sensory cells (hair cells) and associated threshold shifts in
auditory brain stem response (ABR), 2) loss of synaptic connections of the auditory nerve (AN) to inner hair
cells (IHCs) and associated changes in ABR dynamic range, 3) loss of AN cell bodies, and 4) a temporal
processing deficit evidenced by reduced Gap Detection. These are tested at 6, 12, 18 and 24 months of
age in Aim 1, comparing mice with and without either of the noise exposures.
 Aim 1: Assess the progression of ARHL in mice receiving noise exposure at 4 months of age
 compared to age-matched littermates without noise overstimulation.
Our goal is to identify mechanism-based treatments to prevent or reduce ARHL and any acceleration and
enhancement from prior noise exposure. Treatments tested can be started in mid-life (9 mos. old in mice) to
model treatment to Veterans. One treatment targets oxidative stress, using a combination of anti-oxidants
(vitamins A, C, E plus magnesium) already shown to reduce noise-induced hearing loss. A second treatment,
rapamycin, has been shown in our preliminary studies to reduce age-related loss of cochlear sensory cells
(outer hair cells). Both rapamycin and ACEMg are already in clinical application or trails for other purposes.
Side-effects of prolonged rapamycin could limit application in veterans. Aims 2b and c therefore test a
potentially safer rapalog and a potentially safer application period, respectively, to see if they retain efficacy.
 Aim 2a: Determine if ACEMg or rapamycin added to diet at 9 mos. of age will decrease ARHL
 and/or reduce noise acceleration / enhancement of ARHL (tested using Aim 1 metrics); Aim 2b:
 Determine if use of everolimus, a more mTORC1 specific rapalog or Aim 2c: a later (14 mos.)
 intermittent (every 2 weeks) application of rapamycin retains efficacy in reducing ARHL.
Aim 3 uses RNA-Seq to identify the functional signaling pathway targets of the rapamycin effect in reducing
ARHL towards the goal of providing a basis for identification or development of safer rapalogs
 Aim 3: Identify age-related changes in cochlear gene expression and the influence of rapamycin
 on ARHL related functional signaling pathways.

## Key facts

- **NIH application ID:** 9971369
- **Project number:** 5I01RX002431-03
- **Recipient organization:** VETERANS HEALTH ADMINISTRATION
- **Principal Investigator:** Richard Altschuler
- **Activity code:** I01 (R01, R21, SBIR, etc.)
- **Funding institute:** VA
- **Fiscal year:** 2020
- **Award amount:** —
- **Award type:** 5
- **Project period:** 2018-07-01 → 2022-06-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9971369

## Citation

> US National Institutes of Health, RePORTER application 9971369, Prevention of Noise-Induced Acceleration of Age-Related Hearing Loss (5I01RX002431-03). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/9971369. Licensed CC0.

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