Department of Otolaryngology, Kresge Hearing Research Institute, University of Michigan, Ann Arbor, Michigan 48109-5616, USA.
Anat Rec (Hoboken). 2012 Nov;295(11):1837-50. doi: 10.1002/ar.22578. Epub 2012 Oct 8.
This review introduces the pathology of aminoglycoside antibiotic and the cisplatin chemotherapy classes of drugs, discusses oxidative stress in the inner ear as a primary trigger for cell damage, and delineates the ensuing cell death pathways. Among potentially ototoxic (damaging the inner ear) therapeutics, the platinum-based anticancer drugs and the aminoglycoside antibiotics are of critical clinical importance. Both drugs cause sensorineural hearing loss in patients, a side effect that can be reproduced in experimental animals. Hearing loss is reflected primarily in damage to outer hair cells, beginning in the basal turn of the cochlea. In addition, aminoglycosides might affect the vestibular system while cisplatin seems to have a much lower likelihood to do so. Finally, based on an understanding the mechanisms of ototoxicity pharmaceutical ways of protection of the cochlea are presented.
本文介绍了氨基糖苷类抗生素和铂类化疗药物的病理学,讨论了内耳氧化应激作为细胞损伤的主要触发因素,并描述了随后的细胞死亡途径。在潜在的耳毒性(损害内耳)治疗药物中,铂类抗癌药物和氨基糖苷类抗生素具有重要的临床意义。这两种药物都会导致患者出现感音神经性听力损失,这种副作用在实验动物中可以重现。听力损失主要反映在外毛细胞的损伤上,始于耳蜗的基底转。此外,氨基糖苷类药物可能会影响前庭系统,而顺铂似乎不太可能产生这种影响。最后,基于对耳毒性机制的理解,本文提出了保护耳蜗的药物方法。