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本文引用的文献

1
Sox2 up-regulation and glial cell proliferation following degeneration of spiral ganglion neurons in the adult mouse inner ear.成年小鼠内耳螺旋神经节神经元变性后 Sox2 的上调和神经胶质细胞增殖。
J Assoc Res Otolaryngol. 2011 Apr;12(2):151-71. doi: 10.1007/s10162-010-0244-1.
2
The effect of cochlear-implant-mediated electrical stimulation on spiral ganglion cells in congenitally deaf white cats.人工耳蜗电刺激对先天性耳聋白猫螺旋神经节细胞的影响。
J Assoc Res Otolaryngol. 2010 Dec;11(4):587-603. doi: 10.1007/s10162-010-0234-3. Epub 2010 Sep 4.
3
Neurotrophin therapy and cochlear implantation: translating animal models to human therapy.神经营养因子治疗与人工耳蜗植入:从动物模型到临床治疗的转化。
Exp Neurol. 2010 Nov;226(1):1-5. doi: 10.1016/j.expneurol.2010.07.012. Epub 2010 Jul 21.
4
Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.Diaphanous homolog 3 (DIAPH3)/diaphanous 的活性增加会导致患有听觉神经病的人和果蝇出现听力缺陷。
Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13396-401. doi: 10.1073/pnas.1003027107. Epub 2010 Jul 12.
5
Chronic electrical stimulation does not prevent spiral ganglion cell degeneration in deafened guinea pigs.慢性电刺激并不能预防耳聋豚鼠的螺旋神经节细胞变性。
Hear Res. 2010 Oct 1;269(1-2):169-79. doi: 10.1016/j.heares.2010.06.015. Epub 2010 Jun 25.
6
Effects of localized neurotrophin gene expression on spiral ganglion neuron resprouting in the deafened cochlea.局部神经营养因子基因表达对耳聋耳蜗螺旋神经节神经元再生的影响。
Mol Ther. 2010 Jun;18(6):1111-22. doi: 10.1038/mt.2010.28. Epub 2010 Mar 9.
7
Transgenic BDNF induces nerve fiber regrowth into the auditory epithelium in deaf cochleae.转基因 BDNF 诱导耳聋耳蜗中的神经纤维向听觉上皮生长。
Exp Neurol. 2010 Jun;223(2):464-72. doi: 10.1016/j.expneurol.2010.01.011. Epub 2010 Jan 28.
8
Cochlear implantation in children with auditory neuropathy spectrum disorder.听神经病谱系障碍患儿的人工耳蜗植入。
Ear Hear. 2010 Jun;31(3):325-35. doi: 10.1097/AUD.0b013e3181ce693b.
9
Speech and language outcomes in children with auditory neuropathy/dys-synchrony managed with either cochlear implants or hearing aids.听觉神经病/失同步儿童使用人工耳蜗或助听器管理的言语和语言结果。
Int J Audiol. 2009;48(6):313-20. doi: 10.1080/14992020802665959.
10
Adding insult to injury: cochlear nerve degeneration after "temporary" noise-induced hearing loss.雪上加霜:“暂时性”噪声性听力损失后蜗神经变性
J Neurosci. 2009 Nov 11;29(45):14077-85. doi: 10.1523/JNEUROSCI.2845-09.2009.

受损耳蜗中的神经维护和再生。

Nerve maintenance and regeneration in the damaged cochlea.

机构信息

Kresge Hearing Research Institute, Department of Otolaryngology, The University of Michigan, 1150 W. Medical Center Dr., Ann Arbor, MI 48109-5648, USA.

出版信息

Hear Res. 2011 Nov;281(1-2):56-64. doi: 10.1016/j.heares.2011.04.019. Epub 2011 May 10.

DOI:10.1016/j.heares.2011.04.019
PMID:21596129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3196294/
Abstract

Following the onset of sensorineural hearing loss, degeneration of mechanosensitive hair cells and spiral ganglion cells (SGCs) in humans and animals occurs to variable degrees, with a trend for greater neural degeneration with greater duration of deafness. Emergence of the cochlear implant prosthesis has provided much needed aid to many hearing impaired patients and has become a well-recognized therapy worldwide. However, ongoing peripheral nerve fiber regression and subsequent degeneration of SGC bodies can reduce the neural targets of cochlear implant stimulation and diminish its function. There is increasing interest in bio-engineering approaches that aim to enhance cochlear implant efficacy by preventing SGC body degeneration and/or regenerating peripheral nerve fibers into the deaf sensory epithelium. We review the advancements in maintaining and regenerating nerves in damaged animal cochleae, with an emphasis on the therapeutic capacity of neurotrophic factors delivered to the inner ear after an insult. Additionally, we summarize the histological process of neuronal degeneration in the inner ear and describe different animal models that have been employed to study this mechanism. Research on enhancing the biological infrastructure of the deafened cochlea in order to improve cochlear implant efficacy is of immediate clinical importance.

摘要

在感音神经性听力损失发生后,人类和动物的机械敏感毛细胞和螺旋神经节细胞(SGC)会发生不同程度的变性,随着耳聋时间的延长,神经变性的趋势更大。耳蜗植入假体的出现为许多听力受损的患者提供了急需的帮助,并已成为全球公认的治疗方法。然而,外周神经纤维的持续退化和随后的 SGC 体变性会降低耳蜗植入刺激的神经靶标,从而降低其功能。人们越来越关注生物工程方法,旨在通过防止 SGC 体变性和/或再生外周神经纤维进入失聪感觉上皮来提高耳蜗植入的效果。我们回顾了在受损动物耳蜗中维持和再生神经的进展,重点介绍了内耳损伤后神经生长因子的治疗能力。此外,我们总结了内耳神经元变性的组织学过程,并描述了用于研究这种机制的不同动物模型。为了提高耳蜗植入的效果,增强聋耳蜗的生物学基础的研究具有直接的临床意义。