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Published on: March 16, 2018
Protective effect of trimetazidine on amikacin-induced ototoxicity in rats
Fadlullah Aksoy1, Remzi Dogan1, Orhan Ozturan1
1Bezmialem Vakif University, Department of Otorhinolaryngology, Fatih, Istanbul, Turkey.
Objective:
Aminoglycoside antibiotics are known to have ototoxic effects and may induce sensorineural hearing loss. This study investigated the protective effect of trimetazidine, which has antioxidant and cytoprotective properties, against amikacin ototoxicity.
Methods:
Thirty-two male rats were divided into four groups - amikacin, amikacin + trimetazidine, trimetazidine, and control groups. Trimetazidine, 10 mg/kg per day, was given for 14 days by oral gavage. Amikacin, 600 mg/kg per day, was also given for 14 days, by the intramuscular route. Distortion product otoacoustic emission (DPOAE) and auditory brainstem response (ABR) tests were applied to the rats for hearing assessment. At the termination of the study, the biochemical parameters were calculated to evaluate the oxidative status.
Results:
The DPOAE values of the amikacin group were significantly lower on the 7th and 14th days than those of the trimetazidine + amikacin group and there was an increase in the ABR thresholds. The ABR thresholds for the amikacin group on the 7th and 14th days were significantly higher than the levels on the first day of the study, while there was no significant increase in those values in the trimetazidine + amikacin group. The total oxidant status (TOS) and oxidant status index (OSI) values of the amikacin group were significantly higher than those of the trimetazidine + amikacin group. The total antioxidant status (TAS) values of the amikacin group were lower than those of the trimetazidine + amikacin group.
Conclusions:
The audiologic tests and biochemical parameters investigated in this study both point to the protective effect of trimetazidine against amikacin-induced ototoxicity.
Insights
Trimetazidine protects against amikacin-induced ototoxicity. This study shows trimetazidine preserves hearing function and reduces oxidative stress caused by amikacin in rats.
Area of Science:
- Ototoxicity and audiology research.
- Pharmacology of antibiotic-induced hearing loss.
Background:
- Aminoglycoside antibiotics, like amikacin, can cause hearing loss.
- Trimetazidine possesses antioxidant and cytoprotective properties.
Purpose of the Study:
- To investigate the protective effects of trimetazidine against amikacin-induced ototoxicity.
- To assess the impact of trimetazidine on hearing function and oxidative stress markers.
Main Methods:
- Thirty-two male rats were divided into four groups: amikacin, amikacin + trimetazidine, trimetazidine, and control.
- Animals received daily oral trimetazidine (10 mg/kg) or intramuscular amikacin (600 mg/kg) for 14 days.
- Hearing was assessed using distortion product otoacoustic emissions (DPOAE) and auditory brainstem response (ABR); biochemical parameters evaluated oxidative status.
Main Results:
- Amikacin significantly reduced DPOAE values and increased ABR thresholds compared to the control and trimetazidine + amikacin groups.
- Oxidative stress markers (TOS, OSI) were elevated in the amikacin group, while antioxidant status (TAS) was reduced.
- Trimetazidine administration mitigated amikacin's negative effects on hearing and oxidative balance.
Conclusions:
- Trimetazidine demonstrates a protective effect against amikacin-induced ototoxicity.
- The findings suggest trimetazidine's antioxidant properties play a role in preventing aminoglycoside-induced hearing damage.
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