Related Experiment Video
Updated: Jul 12, 2026

12:21
The Mouse Round-window Approach for Ototoxic Agent Delivery: A Rapid and Reliable Technique for Inducing Cochlear Cell Degeneration
Published on: November 26, 2015
Aging does not alter phosphoinositide hydrolysis in the rat cochlear lateral wall
1Department of Otolaryngology, School of Medicine, Keio University, Tokyo, Japan.
Auris, Nasus, Larynx
|March 17, 1999
Summary
Aging does not affect the inositol trisphosphate (InsP3) second messenger system in the cochlear lateral wall. This system, crucial for hearing, shows no age-related changes in purinergic receptor-mediated InsP release in rats.
Area of Science:
- Otolaryngology
- Neuroscience
- Cell Biology
Background:
- The inositol 1,4,5-trisphosphate (InsP3) second messenger system is linked to purinergic P2y receptors in the cochlea.
- Cochlear lateral wall tissues maintain endolymph ionic balance.
- Aging impacts endolymphatic potential and signal transduction, with decreased inositol in sensory epithelia.
Purpose of the Study:
- To compare purinergic receptor-mediated inositol phosphate (InsP) release in the cochlear lateral wall of young and aged rats.
- To investigate the effect of aging on the InsP second messenger system in the cochlear lateral wall.
Main Methods:
- Comparison of InsP release in young (3-month-old) and aged (24-month-old) Fischer-344 rats.
- Measurement of mnyo-[3H]inositol incorporation into phosphoinositide lipids.
- Assessment of purinergic receptor-mediated InsP release.
Main Results:
- No significant differences were observed in mnyo-[3H]inositol incorporation into phosphoinositide lipids between young and aged rats.
- Purinergic receptor-mediated release of inositol phosphates (InsPs) remained unchanged in the cochlear lateral wall of aged rats compared to young rats.
Conclusions:
- The inositol trisphosphate (InsP3) second messenger system in the cochlear lateral wall is not affected by aging.
- This finding contrasts with previous observations in the cochlear sensory epithelium, suggesting age-related resilience in the lateral wall's signaling pathways.

