Sun Changling, Wang Xueling, Chen Dongye, Lin Xin, Yu Dehong, Wu Hao
Department of Otolaryngology-Head and Neck Surgery, Xinhua Hospital, Ear Institute, Shanghai Jiaotong University School of Medicine, Shanghai Key Laboratory of Translational Medicine on Ear and Nose diseases, Shanghai 200092, China; Department of Otolaryngology-Head and Neck Surgery, Affiliated Hospital of Jiangnan University, The Fourth People's Hospital of Wuxi City, Wuxi 214062, China.
Department of Otolaryngology-Head and Neck Surgery, Xinhua Hospital, Ear Institute, Shanghai Jiaotong University School of Medicine, Shanghai Key Laboratory of Translational Medicine on Ear and Nose diseases, Shanghai 200092, China.
Neurosci Lett. 2016 Apr 21;619:142-8. doi: 10.1016/j.neulet.2016.03.012. Epub 2016 Mar 10.
Ototoxicity is one of the most important adverse effects of cisplatin chemotherapy. As a common treatment of acute sensorineural hearing loss, systemic administration of steroids was demonstrated ineffective against cisplatin-induced hearing loss (CIHL) in published studies. The current study aimed to evaluate the potential protective effect of dexamethasone (DEX) encapsulated in polyethyleneglycol-coated polylactic acid (PEG-PLA) nanoparticles (DEX-NPs) against cisplatin-induced hearing loss following systemic administration. DEX was fabricated into PEG-PLA nanoparticles using emulsion and evaporation technique as previously reported. DEX or DEX-NPs was administered intraperitoneally to guinea pigs 1h before cisplatin administration. Auditory brainstem response (ABR) threshold shifts were measured at four frequencies (4, 8, 16, and 24kHz) 1 day before and three days after cisplatin injection. Cochlear morphology was examined to evaluate inner ear injury induced by cisplatin exposure. A single dose of DEX-NPs 1h before cisplatin treatment resulted in a significant preservation of the functional and structural properties of the cochlea, which was equivalent to the effect of multidose (3 days) DEX injection. In contrast, no significant protective effect was observed by single dose injection of DEX. The results of histological examination of the cochleae were consistent with the functional measurements. In conclusion, a single dose DEX-NPs significantly attenuated cisplatin ototoxicity in guinea pigs after systemic administration at both histological and functional levels indicating the potential therapeutic benefits of these nanoparticles for enhancing the delivery of DEX in acute sensorineural hearing loss.
耳毒性是顺铂化疗最重要的不良反应之一。作为急性感音神经性听力损失的常见治疗方法,已发表的研究表明,全身应用类固醇对顺铂所致听力损失(CIHL)无效。本研究旨在评估聚乙二醇包被的聚乳酸(PEG-PLA)纳米颗粒(DEX-NPs)包裹的地塞米松(DEX)在全身给药后对顺铂所致听力损失的潜在保护作用。如先前报道,采用乳化蒸发技术将DEX制成PEG-PLA纳米颗粒。在给予顺铂前1小时,将DEX或DEX-NPs腹腔注射给豚鼠。在顺铂注射前1天和注射后3天,测量四个频率(4、8、16和24kHz)的听觉脑干反应(ABR)阈值变化。检查耳蜗形态以评估顺铂暴露所致的内耳损伤。在顺铂治疗前1小时单次给予DEX-NPs可显著保留耳蜗的功能和结构特性,这与多剂量(3天)注射DEX的效果相当。相比之下,单次注射DEX未观察到明显的保护作用。耳蜗组织学检查结果与功能测量结果一致。总之,单次给予DEX-NPs在全身给药后,在组织学和功能水平上均显著减轻了豚鼠的顺铂耳毒性,表明这些纳米颗粒在急性感音神经性听力损失中增强DEX递送方面具有潜在的治疗益处。