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Aminoglycoside-induced ototoxicity.
- Source :
-
Current pharmaceutical design [Curr Pharm Des] 2007; Vol. 13 (1), pp. 119-26. - Publication Year :
- 2007
-
Abstract
- It has long been known that the major irreversible toxicity of aminoglycosides is ototoxicity. Among them, streptomycin and gentamicin are primarily vestibulotoxic, whereas amikacin, neomycin, dihydrosterptomycin, and kanamicin are primarily cochleotoxic. Cochlear damage can produce permanent hearing loss, and damage to the vestibular apparatus results in dizziness, ataxia, and/or nystagmus. Aminoglycosides appear to generate free radicals within the inner ear, with subsequent permanent damage to sensory cells and neurons, resulting in permanent hearing loss. Two mutations in the mitochondrial 12S ribosomal RNA gene have been previously reported to predispose carriers to aminoglycoside-induced ototoxicity. As aminoglycosides are indispensable agents both in the treatment of infections and Meniere's disease, a great effort has been made to develop strategies to prevent aminoglycoside ototoxicity. Anti-free radical agents, such as salicylate, have been shown to attenuate the ototoxic effects of aminoglycosides. In this paper, incidence, predisposition, mechanism, and prevention of aminoglycoside-induced ototoxicity is discussed in the light of literature data.
- Subjects :
- Aminoglycosides administration & dosage
Aminoglycosides toxicity
Animals
Anti-Bacterial Agents toxicity
Dose-Response Relationship, Drug
Drug Administration Schedule
Genetic Predisposition to Disease
Genetic Testing
Hair Cells, Auditory drug effects
Hearing Disorders genetics
Hearing Disorders prevention & control
Humans
Incidence
Meniere Disease drug therapy
Mutation
RNA genetics
RNA, Mitochondrial
RNA, Ribosomal genetics
Risk Assessment
Risk Factors
Aminoglycosides adverse effects
Anti-Bacterial Agents adverse effects
Cochlea drug effects
Hearing Disorders chemically induced
Vestibule, Labyrinth drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-4286
- Volume :
- 13
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Current pharmaceutical design
- Publication Type :
- Academic Journal
- Accession number :
- 17266591
- Full Text :
- https://doi.org/10.2174/138161207779313731