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脑源性神经营养因子治疗不能改善鸽子毛细胞再生后的功能恢复。

Brain-derived neurotrophic factor treatment does not improve functional recovery after hair cell regeneration in the pigeon.

作者信息

Radeloff A, Smolders J W Th

机构信息

Physiologisches Institut II, Zentrum der Hals-Nasen-Ohrenheilkunde, Frankfurt am Main, Germany.

出版信息

Acta Otolaryngol. 2006 May;126(5):452-9. doi: 10.1080/00016480500437344.

Abstract

CONCLUSIONS

Brain-derived neurotrophic factor (BDNF) supply to the inner ear does not improve the time course or the extent of functional recovery after hair cell regeneration. Specifically it does not improve the residual threshold elevation observed after the completion of spontaneous recovery.

OBJECTIVE

The avian inner ear is capable of hair cell regeneration and substantial functional recovery, but residual hearing deficits remain. We investigated whether functional recovery can be improved by intracochlear application of BDNF, which plays an important role in auditory ontogenesis and maintenance during adult life.

METHODS

Hair cells in adult pigeons were destroyed by local application of gentamicin. After 3 days either BDNF or control solution was administered to the scala tympani by implanted osmotic minipumps for 8 weeks. Auditory brain stem responses (ABR) to tone pips were used to assess recovery of hearing thresholds in both groups.

RESULTS

The application of gentamicin caused a frequency-dependent hearing loss that ranged from 24.8 dB SPL at low frequencies to 66.2 dB SPL at high frequencies. After day 10 substantial recovery was observed, but a significant threshold shift remained. The time course of recovery in the control and BDNF-treated groups was similar, without significant residual threshold differences in any frequency range.

摘要

结论

向内耳提供脑源性神经营养因子(BDNF)并不能改善毛细胞再生后功能恢复的时间进程或程度。具体而言,它不能改善自发恢复完成后观察到的残余阈值升高。

目的

鸟类内耳能够进行毛细胞再生和显著的功能恢复,但仍存在残余听力缺陷。我们研究了通过在耳蜗内应用BDNF是否可以改善功能恢复,BDNF在听觉发育和成年期维持中起重要作用。

方法

通过局部应用庆大霉素破坏成年鸽子的毛细胞。3天后,通过植入的渗透微型泵向鼓阶给予BDNF或对照溶液,持续8周。使用对短纯音的听觉脑干反应(ABR)评估两组的听力阈值恢复情况。

结果

庆大霉素的应用导致了频率依赖性听力损失,低频范围为24.8 dB SPL,高频范围为66.2 dB SPL。在第10天后观察到显著恢复,但仍存在明显的阈值偏移。对照组和BDNF治疗组的恢复时间进程相似,在任何频率范围内均无显著的残余阈值差异。

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