Kanamycin induces free radicals formation in melanocytes: An important factor for aminoglycosides ototoxicity

Dorota Wrześniok1, Jakub Rok1, Artur Beberok1

  • 1Department of Pharmaceutical Chemistry, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia in Katowice, Sosnowiec, Poland.

Insights

Kanamycin antibiotic causes oxidative stress and melanin loss in dark melanocytes, contributing to hearing loss. This study investigated the role of melanin in kanamycin-induced ototoxicity.

Area of Science:

  • Ototoxicity
  • Melanocyte Biology
  • Free Radical Chemistry

Background:

  • Aminoglycoside antibiotics like kanamycin can cause ototoxicity, a hearing impairment.
  • Melanin, a pigment found in skin, hair, eyes, and the inner ear, may influence this side effect.
  • Previous studies showed kanamycin disrupts light-pigmented melanocytes; this study examines dark melanocytes.

Purpose of the Study:

  • To investigate the role of melanization in kanamycin-induced ototoxicity.
  • To determine if kanamycin affects dark-pigmented melanocytes (HEMn-DP) and melanin content.

Main Methods:

  • In vitro study using dark-pigmented melanocytes (HEMn-DP).
  • Spectrophotometric measurements and electron paramagnetic resonance (EPR) spectroscopy.
  • Assessed cell viability, antioxidant enzyme activity, free radical production, and melanin content.

Main Results:

  • Kanamycin induced a concentration-dependent loss of melanocyte viability (IC50 = 5.0 mM).
  • Observed modulation of antioxidant enzymes, increased free radical production, and decreased melanin content.
  • Confirmed kanamycin generates oxidative stress in melanocytes.

Conclusions:

  • Kanamycin-induced oxidative stress and free radical production contribute to impaired antioxidant defense and reduced melanin in melanocytes.
  • Melanin content in melanocytes may play a role in the mechanism of kanamycin-induced hearing impairment.

Related Concept Videos

Radical Formation: Abstraction00:47

Radical Formation: Abstraction

The electron of an atom can be abstracted from a compound by a relatively unstable radical to generate a new radical of relatively greater stability. For example, an initiator which forms radicals by homolysis can abstract a suitable species like a hydrogen atom or a halogen atom from a compound to generate a new radical. This ability of radicals to propagate by abstraction is a crucial feature of radical chain reactions.
Even though homolysis produces radicals, it is different from radical...
4.4K
Radical Formation: Elimination00:51

Radical Formation: Elimination

Another method of radical formation is the elimination process. It is the opposite of the addition route and is driven by the instability of the radical. For example, as depicted in Figure 1, dibenzoyl peroxide yields a pair of unstable radicals upon homolysis. Given its instability, this radical spontaneously undergoes elimination via a C–C bond cleavage to form a relatively more stable phenyl radical. The mechanism involves cleavage of the bond between the α and β positions with respect...
2.4K
Radical Formation: Overview01:03

Radical Formation: Overview

A bond can be broken either by heterolytic bond cleavage to form ions or homolytic bond cleavage to yield radicals. A fishhook arrow is used to represent the motion of a single electron in homolytic bond cleavage. There are two main sources from which radicals can be formed:
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
2.7K
Radical Formation: Homolysis00:54

Radical Formation: Homolysis

A bond is formed between two atoms by sharing two electrons. When this bond is broken by supplying sufficient energy, either two electrons can be taken up by one atom forming ions by the cleavage called heterolysis, or the two electrons are shared by two atoms, with one each creating radicals by the cleavage called homolysis.
4.5K
Radical Formation: Addition00:47

Radical Formation: Addition

Radicals can be formed by adding a radical to a spin-paired molecule. This is typically observed with unsaturated species, where the addition of a radical across the π bond leads to the production of a new radical by dissolving the π bond. For example, the addition of a Br radical to an alkene yields a carbon-centered radical.
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...
2.3K
Estimation of k and VD of Aminoglycosides01:20

Estimation of k and VD of Aminoglycosides

Aminoglycosides are a class of antibiotics used to treat various bacterial infections. Clinicians must determine the elimination rate constant (k) and volume of distribution (VD) to optimize therapeutic efficacy and minimize toxicity. The k value represents the rate at which the drug is removed from the body, and the VD reflects the degree to which the drug distributes into body tissues. Accurately estimating these parameters allows healthcare professionals to tailor drug dosing to individual...
244