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

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 Insomnia01:19

Management of Insomnia

The sleep cycle, an integral part of human health, consists of several stages with distinct characteristics and functions. It begins with a transition from wakefulness to sleep, known as the light sleep phase, followed by the restorative deep sleep phase, essential for physical recovery and growth. The cycle concludes with the Rapid Eye Movement (REM) phase, characterized by high brain activity and vivid dreaming. Insomnia, a prevalent sleep disorder, involves difficulty falling asleep, staying...
Sedatives and Hypnotics Drugs: Miscellaneous Agents01:17

Sedatives and Hypnotics Drugs: Miscellaneous Agents

Sedatives and hypnotics encompass a wide range of substances, each with its unique mechanism of action, uses, and potential adverse effects.
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 Response01:15

Chronopharmacokinetics: Circadian Rhythms and Influence on Drug Response

Circadian rhythms are cyclic changes that are crucial in plasma drug concentrations. Various standard circadian parameters, including core body temperature, heart rate, and other cardiovascular factors, directly impact disease states and the therapeutic response to drug therapy.
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: Overview01:23

Sedatives and Hypnotics: Overview

Sedatives are drugs that alleviate anxiety, while hypnotics induce sleep. Both classes of medication suppress neuronal activity, leading to a calming effect for sedatives and facilitating sleep for hypnotics.
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 Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...
Therapeutic Drug Monitoring: Overview and Classification01:16

Therapeutic Drug Monitoring: Overview and Classification

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood at designated intervals to ensure the drug concentration stays within a therapeutic range. This monitoring is crucial for optimizing individual dosage regimens, enhancing therapeutic efficacy, and minimizing drug-related toxicity. TDM is vital for drugs with narrow therapeutic windows, significant variability in pharmacokinetics, and a clear correlation between plasma levels and...