Related Experiment Video
Updated: Sep 24, 2025

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
Tetrandrine Prevents Neomycin-Induced Ototoxicity by Promoting Steroid Biosynthesis
Qilei Zhang1, Yunhao Wu2, Yan Yu1
1The Affiliated Zhangjiagang Hospital of Soochow University, Zhangjiagang, China.
Abstract:
Aminoglycoside antibiotics are widely used for the treatment of serious acute infections, life-threatening sepsis, and tuberculosis, but all aminoglycosides cause side effects, especially irreversible ototoxicity. The mechanisms underlying the ototoxicity of aminoglycosides need further investigation, and there are no effective drugs in the clinic. Here we showed that tetrandrine (TET), a bioactive bisbenzylisoquinoline alkaloid derived from Stephania tetrandra, ameliorated neomycin-induced cochlear hair cell injury. In both in vitro and in vivo experiments we found that TET administration significantly improved auditory function and reduced hair cell damage after neomycin exposure. In addition, we observed that TET could significantly decrease oxidative stress and apoptosis in hair cells after neomycin exposure. Finally, RNA-seq analysis suggested that TET protected against neomycin-induced ototoxicity mainly by promoting steroid biosynthesis. Collectively, our results provide pharmacological evidence showing that TET may be a promising agent in preventing aminoglycosides-induced ototoxicity.
Insights
Tetrandrine (TET) may prevent hearing loss caused by aminoglycoside antibiotics. This study found TET administration improved auditory function and reduced hair cell damage in models of neomycin-induced ototoxicity.
Area of Science:
- Pharmacology
- Ototoxicity Research
- Drug Discovery
Background:
- Aminoglycoside antibiotics are crucial for treating severe infections but cause irreversible ototoxicity.
- Current treatments lack effective strategies to prevent or mitigate aminoglycoside-induced ototoxicity.
Purpose of the Study:
- To investigate the protective effects of tetrandrine (TET) against neomycin-induced ototoxicity.
- To elucidate the underlying mechanisms of TET's protective action.
Main Methods:
- In vitro and in vivo experiments using neomycin-induced ototoxicity models.
- Assessment of auditory function and cochlear hair cell damage.
- Analysis of oxidative stress, apoptosis, and gene expression (RNA-seq).
Main Results:
- TET administration significantly improved auditory function and reduced hair cell injury.
- TET decreased oxidative stress and apoptosis in cochlear hair cells.
- RNA-seq analysis indicated TET promotes steroid biosynthesis, a potential protective pathway.
Conclusions:
- Tetrandrine shows promise as a therapeutic agent to prevent aminoglycoside-induced ototoxicity.
- TET's protective effects may be mediated by promoting steroid biosynthesis and reducing cellular stress and apoptosis.
More Related Videos
09:06Cochlear Implant Surgery and Electrically-evoked Auditory Brainstem Response Recordings in C57BL/6 Mice
Published on: January 9, 2019
11:00Methods to Inhibit Bacterial Pyomelanin Production and Determine the Corresponding Increase in Sensitivity to Oxidative Stress
Published on: August 31, 2015
Related Concept Videos
Drugs that Stabilize Microtubules
Drugs that Destabilize Microtubules
Drugs Affecting Neurotransmitter Synthesis
Desensitization and Tachyphylaxis
Combined Effects of Drugs: Synergism
Such synergistic combinations...
Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists