Anniko M, Takada A, Schacht J
Am J Otolaryngol. 1982 Nov-Dec;3(6):422-33. doi: 10.1016/s0196-0709(82)80020-3.
The ototoxic potentials of netilmicin and gentamicin were compared in three models: the standard in-vivo animal model (guinea pig), organ culture of the embryonic inner ear (mouse), and perilymphatic perfusions (guinea pig). Toxicity was assessed by light and electron microscopy of hair cells or by measurement of cochlear microphonic potentials. In vivo, netilmicin did not have any significant morphologic effect on hair cells under conditions (dose X duration) where gentamicin caused excessive hair cell loss. In organ culture, concentrations of netilmicin had to be at least tenfold higher than those of gentamicin in order to produce comparable damage. In direct applications of the drugs to the cochlea by perilymphatic perfusion, similar effects on cochlear microphonics were seen when netilmicin concentrations were more than threefold higher than those of gentamicin. It is suggested that netilmicin ototoxicity observed in vivo is low because of lesser penetration into the inner ear and lower intrinsic toxicity.
标准体内动物模型(豚鼠)、胚胎内耳器官培养(小鼠)和外淋巴灌注(豚鼠)。通过毛细胞的光学和电子显微镜检查或通过测量耳蜗微音器电位来评估毒性。在体内,在庆大霉素导致大量毛细胞损失的条件(剂量×持续时间)下,奈替米星对毛细胞没有任何显著的形态学影响。在器官培养中,奈替米星的浓度必须比庆大霉素至少高10倍才能产生相当的损伤。在通过外淋巴灌注将药物直接应用于耳蜗时,当奈替米星浓度比庆大霉素高3倍以上时,观察到对耳蜗微音器有类似的影响。有人认为,体内观察到的奈替米星耳毒性较低是因为其向内耳的渗透较少且内在毒性较低。