Ototoxicity of kanamycin sulfate in adult rats and its underlying mechanisms.
- Author:
Zhi-Cun ZHANG
1
;
Hong-Meng YU
;
Quan LIU
;
Jie TIAN
;
Tian-Feng WANG
;
Chui-Jin LAI
;
Xiao-Ya ZHOU
Author Information
1. Department of Otolaryngology and Central Laboratory, Fudan University, Shanghai 200031, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Cochlea;
drug effects;
pathology;
Evoked Potentials, Auditory, Brain Stem;
drug effects;
Hair Cells, Auditory, Outer;
cytology;
drug effects;
pathology;
Hearing Loss;
chemically induced;
physiopathology;
Kanamycin;
toxicity;
Male;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Spiral Ganglion;
pathology;
physiology;
ultrastructure
- From:
Acta Physiologica Sinica
2011;63(2):171-176
- CountryChina
- Language:Chinese
-
Abstract:
The aim of the present study was to assess the ototoxicity of kanamycin sulfate (KM) in adult rats and its underlying mechanism. Forty male Sprague-Dawley rats (6-7 weeks old) were randomly divided into the experimental group and the control group. The animals in the experimental group were injected subcutaneously with KM (500 mg/kg per day) for two weeks, and the control group received equal volume of normal saline. To assess the ototoxicity of KM, the auditory brainstem response (ABR) was recorded to monitor the changes in hearing thresholds, and the density of spiral ganglion cells (SGCs) and morphology of cochlea were observed using surface preparations and frozen sections of cochlea. The results showed that the hearing threshold of rats in the experimental group was elevated by more than 60 dB across all the frequencies two weeks after the first administration of KM. And in the experimental group, the density of SGCs became lower, and organ of Corti suffered loss of hair cells. The loss of outer hair cells (OHCs) was more severe than that of inner hair cells (IHCs), correlated with the density decrease of SGCs. We conclude that the ototoxicity of KM in the adult rats was apparent and the underlying mechanism is associated with the loss of SGCs and hair cells.
