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Updated: May 14, 2026

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model
Published on: September 7, 2013
Modulation of melanogenesis and antioxidant defense system in melanocytes by amikacin
Dorota Wrześniok1, Artur Beberok, Michał Otręba
1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University of Silesia, Jagiellońska 4, PL 41-200 Sosnowiec, Poland.
Abstract:
Amikacin is principally used to treat infections caused by microorganisms resistant to other aminoglycosides. Ototoxicity is one of the side effects of amikacin, but the causative mechanism of damage to the ear has not been fully established. Thus, the aim of this work was to examine the impact of amikacin on the melanogenesis and antioxidant defense system in cultured human normal melanocytes (HEMa-LP). Amikacin induced the concentration - dependent loss in melanocytes viability. The value of EC50 was determined to be ~7.5 mM. The analyzed antibiotic inhibited melanin biosynthesis in concentration-dependent manner. Increasing the amikacin concentration also resulted in a decrease in cellular tyrosinase activity. To study the antioxidant defense system in melanocytes, the activities of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) in cells exposed to amikacin were determined. Significant changes in cellular antioxidant enzymes activities were observed. Modulation of melanogenesis and the antioxidant status of melanocytes resulting from the use of amikacin in vitro may explain a potential role of melanin and melanocytes in the mechanisms of aminoglycosides ototoxic effects in vivo.
Insights
Amikacin antibiotic use may harm hearing by affecting melanin production and antioxidant defenses in melanocytes, potentially explaining ototoxicity. Further research is needed to understand these mechanisms.
Area of Science:
- Cell Biology
- Pharmacology
- Toxicology
Background:
- Amikacin is an important antibiotic for treating resistant infections.
- Ototoxicity is a known side effect of amikacin, but its mechanism is unclear.
Purpose of the Study:
- To investigate amikacin's effects on melanogenesis and antioxidant defense in human melanocytes.
- To explore the potential role of melanocytes in amikacin-induced ototoxicity.
Main Methods:
- Cultured human normal melanocytes (HEMa-LP) were exposed to varying concentrations of amikacin.
- Cell viability, melanin biosynthesis, tyrosinase activity, and antioxidant enzyme activities (SOD, CAT, GPx) were measured.
Main Results:
- Amikacin reduced melanocyte viability in a dose-dependent manner (EC50 ~7.5 mM).
- Melanin production and tyrosinase activity were inhibited by amikacin.
- Activities of cellular antioxidant enzymes superoxide dismutase, catalase, and glutathione peroxidase were significantly altered.
Conclusions:
- Amikacin impacts melanogenesis and antioxidant status in melanocytes.
- These findings suggest melanocytes and melanin may play a role in the ototoxic effects of aminoglycosides like amikacin.
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