Related Experiment Video
Updated: Jun 1, 2026

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
Drug-mediated ototoxicity and tinnitus: alleviation with melatonin
R J Reiter1, D-X Tan, A Korkmaz
1Department of Cellular and Structural Biology, The University of Texas Health Science Center, San Antonio, TX 78229, USA. reiter@uthscsa.edu
Abstract:
This review evaluates the published basic science and clinical reports related to the role of melatonin in reducing the side effects of aminoglycosides and the cancer chemotherapeutic agent cisplatin, in the cochlea and vestibule of the inner ear. A thorough search of the literature was performed using available databases for the purpose of uncovering articles applicable to the current review. Cochlear function was most frequently evaluated by measuring otoacoustic emissions and their distortion products after animals were treated with cytotoxic drugs alone or in combination with melatonin. Vestibular damage due to aminoglycosides was evaluated by estimating hair cell loss in explanted utricles of newborn rats. Tinnitus was assessed in patients who received melatonin using a visual analogue scale or the Tinnitus Handicap Inventory. Compared to a mixture of antioxidants which included tocopherol, ascorbate, glutathione and N-acetyl-cysteine, melatonin, also a documented antioxidant, was estimated to be up to 150 times more effective in limiting the cochlear side effects, evaluated using otoacoustic emission distortion products, of gentamicin, tobramycin and cisplatin. In a dose-response manner, melatonin also reduced vestibular hair cell loss due to gentamicin treatment in explanted utricles of newborn rats. Finally, melatonin (3 mg daily) limited subjective tinnitus in patients. These findings suggest the potential use of melatonin to combat the ototoxicity of aminoglycosides and cancer chemotherapeutic agents. Additional studies at both the experimental and clinical levels should be performed to further document the actions of melatonin at the cochlear and vestibular levels to further clarify the protective mechanisms of action of this ubiquitously-acting molecule. Melatonin's low cost and minimal toxicity profile supports its use to protect the inner ear from drug-mediated damage.
Insights
Melatonin, a potent antioxidant, significantly reduces inner ear damage caused by ototoxic drugs like aminoglycosides and cisplatin. This molecule shows promise in preventing hearing loss and tinnitus, with minimal toxicity.
Area of Science:
- Ototoxicity research
- Inner ear drug side effects
- Melatonin pharmacology
Background:
- Aminoglycosides and cisplatin cause cochlear and vestibular damage.
- Ototoxicity leads to hearing loss, tinnitus, and balance disorders.
- Melatonin is a known antioxidant with potential protective properties.
Purpose of the Study:
- To review the role of melatonin in mitigating aminoglycoside and cisplatin ototoxicity.
- To evaluate melatonin's efficacy in protecting the cochlea and vestibule.
- To assess melatonin's impact on drug-induced tinnitus.
Main Methods:
- Literature review of basic science and clinical studies.
- Evaluation of cochlear function using otoacoustic emissions.
- Assessment of vestibular damage via hair cell loss in rat utricles.
- Tinnitus assessment in patients using validated scales.
Main Results:
- Melatonin was up to 150 times more effective than other antioxidants in preventing cochlear damage from gentamicin, tobramycin, and cisplatin.
- Melatonin demonstrated a dose-dependent reduction in vestibular hair cell loss induced by gentamicin.
- A daily dose of 3 mg melatonin effectively reduced subjective tinnitus in patients.
Conclusions:
- Melatonin shows significant potential for preventing drug-induced ototoxicity.
- Further experimental and clinical studies are warranted to elucidate melatonin's protective mechanisms.
- Melatonin's low cost and safety profile make it a viable option for inner ear protection.
Related Concept Videos
Management of Insomnia
Sedatives and Hypnotics Drugs: Miscellaneous Agents
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Chronopharmacokinetics: Circadian Rhythms and Influence on Drug Response
The time of drug administration is an important factor to consider, as it can influence the toxic dose of a drug. For example, a study conducted by Prins et al. in 1997 examined the effects of the timing of...
Sedatives and Hypnotics: Overview
Sedative-hypnotics are categorized into barbiturates, benzodiazepines (BZDs), and non-benzodiazepines or Z-drugs. These drugs work by suppressing central nervous system activity, and this suppression is dose-dependent. Older sedative medications, like barbiturates, follow a linear curve in...
Drug Toxicity: Dose-Dependent Reactions
Therapeutic Drug Monitoring: Overview and Classification

