Sound Pharmaceuticals, Inc 4010 Stone Way N., Suite 120, Seattle, WA 98103, USA.
Sound Pharmaceuticals, Inc 4010 Stone Way N., Suite 120, Seattle, WA 98103, USA.
J Cyst Fibros. 2021 Mar;20(2):271-277. doi: 10.1016/j.jcf.2020.02.014. Epub 2020 Mar 5.
Cystic fibrosis patients are often adminstered tobramycin to treat pulmonary infections. Unfortunately, a common side effect is hearing loss, which can fluctuate. Ebselen has known anti-inflammatory properties and could reduce the incidence and severity of tobramycin-induced hearing loss.
In vitro: neonatal cochlear cultures were treated with tobramycin or cotreated with tobramycin and ebselen for 3 days. In vivo: adult mice were injected with tobramycin or tobramycin and ebselen for 14 days. ABRs were collected in a repeated measures design until 56 days after treatments. ABR threshold shifts were analyzed and a novel cochleotoxic criteria applied to determine the incidence of ototoxicity. Cochlear immunohistology was analyzed for IHC and OHC loss.
Tobramycin leads to significant IHC and OHC loss in cochlear explant cultures. Ebselen co-treatment at 1:20 concentrations resulted in significant otoprotection. Tobramycin leads to significant ABR threshold shifts that are ameliorated by ebselen co-treatment. Hearing loss did not correlate with significant IHC or OHC loss.
This mouse model of tobramycin-induced ototoxicity is clinically relevant in that it results in an incidence and severity of hearing loss recently documented in clinic. The in vitro experiments show that tobramycin kills hair cells and that ebselen co-treatment can attenuate this ototoxicity. The in vivo model shows tobramycin-induced hearing loss is ameliorated by ebselen co-treatment, but this is not explained by concomitant hair cell loss. These preclinical data support the testing of ebselen in CF patients receiving tobramycin treatment.
囊性纤维化患者常接受妥布霉素治疗肺部感染。不幸的是,常见的副作用是听力损失,且这种损失可能波动。艾地苯醌具有已知的抗炎特性,可降低妥布霉素引起的听力损失的发生率和严重程度。
体外:用妥布霉素或妥布霉素和艾地苯醌共同处理新生耳蜗培养物 3 天。体内:用妥布霉素或妥布霉素和艾地苯醌给成年小鼠注射 14 天。采用重复测量设计收集 ABR,直至治疗后 56 天。分析 ABR 阈值变化,并应用新的耳蜗毒性标准来确定耳毒性的发生率。对耳蜗免疫组织化学进行分析,以检测 IHC 和 OHC 的损失。
妥布霉素导致耳蜗离体培养物中的 IHC 和 OHC 显著丢失。以 1:20 浓度共同给予艾地苯醌可显著发挥耳保护作用。妥布霉素导致明显的 ABR 阈值变化,而艾地苯醌共同处理可改善这些变化。听力损失与 IHC 或 OHC 的显著丢失无关。
该妥布霉素诱导的耳毒性小鼠模型在临床上具有相关性,因为它导致了最近在临床中记录到的听力损失的发生率和严重程度。体外实验表明,妥布霉素可杀死毛细胞,而艾地苯醌共同处理可减轻这种耳毒性。体内模型表明,艾地苯醌共同处理可改善妥布霉素引起的听力损失,但这不能用伴随的毛细胞损失来解释。这些临床前数据支持在接受妥布霉素治疗的 CF 患者中测试艾地苯醌。