McCormick G C, Weinberg E, Szot R J, Schwartz E
Toxicol Appl Pharmacol. 1985 Mar 15;77(3):479-89. doi: 10.1016/0041-008x(85)90188-7.
Netilmicin, a semisynthetic aminoglycoside antibiotic, is less ototoxic in a variety of species than other aminoglycosides currently in therapeutic use. In this study, mixed-breed cats (four/group) were given daily sc injections of netilmicin (20, 40, and 80 mg/kg), gentamicin (20 and 40 mg/kg), or tobramycin (20, 40, and 80 mg/kg) for up to 30 weeks or until ototoxicity was observed. The animals were examined throughout the study for effects on cochlear and vestibular function. Hematologic, serum chemical, and drug-serum (24-hr postdose) assays were performed at approximate monthly intervals during the dosing period. The cochleae, kidneys, and liver were examined microscopically. The mean number of dose days required to produce vestibulotoxic effects, demonstrated by impaired righting reflex or locomotor ataxia, was from 41 to 61 in cats dosed with tobramycin (40 and 80 mg/kg) or gentamicin. No vestibular dysfunction was observed in any of the netilmicin 20-mg/kg-dosed cats, in two cats each of the tobramycin 20-mg/kg and netilmicin 40-mg/kg groups, and in one netilmicin 80-mg/kg-dosed animal. Histologic examination of the cochleae revealed degeneration of the hair cells and supporting sensory structures in the majority of cats dosed with gentamicin at 20 and 40 mg/kg and tobramycin at 40 and 80 mg/kg. Less than 50% of the tissues from cats of the tobramycin 20-mg/kg and netilmicin 40- and 80-mg/kg-dosed groups had similar degenerative cochlear changes. No cochlear damage was noted in any of the cats given netilmicin at 20 mg/kg. Results of the clinical laboratory determinations were generally unremarkable. Proximal tubular degeneration was the principal finding observed in the kidneys of the animals. Under the conditions of this study, at least a twofold (vestibular) to fourfold (cochlear) relative safety margin for ototoxicity was established in favor of netilmicin over tobramycin and gentamicin.
奈替米星是一种半合成氨基糖苷类抗生素,与目前治疗中使用的其他氨基糖苷类药物相比,在多种物种中其耳毒性较小。在本研究中,对杂种猫(每组4只)每日皮下注射奈替米星(20、40和80mg/kg)、庆大霉素(20和40mg/kg)或妥布霉素(20、40和80mg/kg),持续30周或直至观察到耳毒性。在整个研究过程中对动物进行检查,以观察对耳蜗和前庭功能的影响。在给药期间,大约每月进行一次血液学、血清化学和药物血清(给药后24小时)检测。对耳蜗、肾脏和肝脏进行显微镜检查。给予妥布霉素(40和80mg/kg)或庆大霉素的猫产生前庭毒性作用(表现为翻正反射受损或运动性共济失调)所需的平均给药天数为41至61天。在任何接受20mg/kg奈替米星给药的猫、妥布霉素20mg/kg组和奈替米星40mg/kg组的每两只猫以及一只接受80mg/kg奈替米星给药的动物中均未观察到前庭功能障碍。对耳蜗的组织学检查显示,大多数接受20和40mg/kg庆大霉素以及40和80mg/kg妥布霉素给药的猫的毛细胞和支持感觉结构发生退化。妥布霉素20mg/kg组以及奈替米星40和80mg/kg给药组的猫中,不到50%的组织有类似的耳蜗退化变化。在任何接受20mg/kg奈替米星给药的猫中均未发现耳蜗损伤。临床实验室检测结果一般无明显异常。近端肾小管变性是在动物肾脏中观察到的主要发现。在本研究条件下,相对于妥布霉素和庆大霉素,奈替米星在耳毒性方面建立了至少两倍(前庭)至四倍(耳蜗)的相对安全 margin。