Henley C M, Schacht J
Kresge Hearing Research Institute, University of Michigan, Ann Arbor.
Audiology. 1988;27(3):137-46. doi: 10.3109/00206098809081584.
This review critically evaluates the literature on aminoglycoside pharmacokinetics in order to answer the question how fluid and tissue levels of the drugs relate to the development of ototoxic and nephrotoxic side effects. We will summarize the evidence that: (1) aminoglycosides do not accumulate in inner-ear fluids; (2) aminoglycoside levels in fluids do not correlate with the ototoxic potential of a drug, and (3) selective toxicity cannot be explained by selective tissue penetration of the drugs. We suggest that studies of drug disposition at the cellular level after chronic aminoglycoside treatment be conducted to establish whether a cell-specific uptake contributes to the selective toxicity of the aminoglycoside antibiotics. A sequence of biochemical events that may lead to the development of toxicity at the molecular level is briefly described.
本综述对氨基糖苷类药物的药代动力学文献进行了批判性评估,以回答药物的体液和组织水平与耳毒性和肾毒性副作用的发生之间有何关系这一问题。我们将总结以下证据:(1)氨基糖苷类药物不会在内耳液中蓄积;(2)体液中的氨基糖苷类药物水平与药物的耳毒性潜力无关;(3)选择性毒性无法用药物的选择性组织渗透来解释。我们建议开展慢性氨基糖苷类药物治疗后细胞水平的药物处置研究,以确定细胞特异性摄取是否导致了氨基糖苷类抗生素的选择性毒性。本文还简要描述了一系列可能在分子水平导致毒性发生的生化事件。