使用地塞米松洗脱电极阵列的人工耳蜗可减少人工耳蜗植入小鼠模型和人体的异物反应。

Muhammad Taifur Rahman, Brian Mostaert, Peter Eckard, Shakila Mahmuda Fatima, Rachel Scheperle, Ibrahim Razu, Bryce Hunger, Rafal T Olszewski, Shoujun Gu, Cristina Garcia, Nashwaan Ali Khan, Douglas M Bennion, Jacob Oleson, Jonathon R Kirk, Ya Lang Enke, Robert D Gay, Robert J Morell, Keiko Hirose, Michael Hoa, Alexander D Claussen, Marlan R Hansen
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摘要

人工耳蜗植入术(CI)后的炎性异物反应(FBR)会对 CI 效果产生负面影响,包括电极阻抗增加。本研究旨在研究地塞米松洗脱人工耳蜗植入体和局部给药地塞米松(一种强效抗炎糖皮质激素)对小鼠模型和人类受试者植入后耳蜗内异物反应和电阻抗的长期疗效。CX3CR1 +/GFP Thy1 +/YFP(巨噬细胞-神经元双报告因子)小鼠的左耳植入地塞米松洗脱耳蜗植入体(Dex-CI)或标准植入体(Standard-CI),右耳作为未手术对照。另一组双报告小鼠植入了标准 CI 电极阵列,然后在中耳注射地塞米松,以模拟当前的临床实践(Dex-local)。对植入的小鼠进行电刺激,并连续测量电阻抗。给人类受试者植入标准或 Dex-CI 后进行连续阻抗测量。Dex-CI 降低了小鼠模型和人类受试者的电阻抗,并在小鼠模型中延长了炎性 FBR 的持续时间。在小鼠模型中,局部地塞米松对长期降低 FBR 和电极阻抗无效。我们的数据表明,地塞米松洗脱阵列比目前临床上局部应用地塞米松更能有效降低 FBR 和电阻抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cochlear implants with dexamethasone-eluting electrode arrays reduce foreign body response in a murine model of cochlear implantation and human subjects.

The inflammatory foreign body response (FBR) following cochlear implantation (CI) can negatively impact CI outcomes, including increased electrode impedances. This study aims to investigate the long-term efficacy of dexamethasone eluting cochlear implant and locally delivered dexamethasone, a potent anti-inflammatory glucocorticoid on the intracochlear FBR and electrical impedance post-implantation in a murine model and human subjects. The left ears of CX3CR1 +/GFP Thy1 +/YFP (macrophage-neuron dual reporter) mice were implanted with dexamethasone-eluting cochlear implants (Dex-CI) or standard implant (Standard-CI) while the right ear served as unoperated control. Another group of dual reporter mice was implanted with a standard CI electrode array followed by injection of dexamethasone in the middle ear to mimic current clinical practice (Dex-local). Mouse implants were electrically stimulated with serial measurement of electrical impedance. Human subjects were implanted with either standard or Dex-CI followed by serial impedance measurements. Dex-CI reduced electrical impedance in the murine model and human subjects and inflammatory FBR in the murine model for an extended period. Dex-local in the murine model is ineffective for long-term reduction of FBR and electrode impedance. Our data suggest that dexamethasone eluting arrays are more effective than the current clinical practice of locally applied dexamethasone in reducing FBR and electrical impedance.

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