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局部 GDNF 给药对内耳聋豚鼠的治疗后影响。

Post-treatment effects of local GDNF administration to the inner ears of deafened guinea pigs.

机构信息

Center for Hearing and Communication Research and Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Neurotrauma. 2010 Sep;27(9):1745-51. doi: 10.1089/neu.2009.1218.

Abstract

For patients with profound hearing loss, a cochlear implant is the only treatment available today. The function of a cochlear implant depends in part on the function and survival of spiral ganglion neurons. Following deafferentation, glial cell-derived neurotrophic factor (GDNF) is known to affect spiral ganglion neuron survival. The purpose of this study was to assess delayed GDNF treatment after deafening, the effects of cessation of GDNF treatment, and the effects of subsequent antioxidants on responsiveness and survival of the spiral ganglion neurons. Three-week deafened (by local neomycin administration) guinea pigs were implanted in the scala tympani with a combined cochlear implant electrode and cannula. GDNF (1 μg/mL) or artificial perilymph was then delivered for 4 weeks, following which the animals received systemic ascorbic acid  +  Trolox or saline for an additional 4 weeks. Thresholds for electrically-evoked auditory brain stem responses (eABRs) were significantly elevated at 3 weeks with deafness, stabilized with GDNF, and showed no change with GDNF cessation and treatment with antioxidants or saline. The populations of spiral ganglion neurons were reduced with deafness (by 40% at 3 weeks and 70% at 11 weeks), and rescued from cell death by GDNF with no further reduction at 8 weeks following 4 weeks of cessation of GDNF treatment equally in both the antioxidant- and saline-treated groups. Local growth factor treatment of the deaf ear may prevent deterioration in electrical responsiveness and rescue auditory nerve cells from death; these effects outlast the period of treatment, and may enhance the benefits of cochlear implant therapy for the deaf.

摘要

对于深度听力损失的患者,目前唯一可用的治疗方法是耳蜗植入。耳蜗植入的功能部分取决于螺旋神经节神经元的功能和存活。去传入后,胶质细胞源性神经营养因子 (GDNF) 已知会影响螺旋神经节神经元的存活。本研究的目的是评估失聪后延迟的 GDNF 治疗、停止 GDNF 治疗的影响以及随后抗氧化剂对螺旋神经节神经元反应性和存活的影响。将三周聋的(通过局部新霉素给药)豚鼠植入耳蜗植入电极和套管的鼓阶。然后用 1μg/mL 的 GDNF 或人工外淋巴液治疗 4 周,之后动物接受全身抗坏血酸+ Trolox 或生理盐水治疗另外 4 周。电诱发听脑干反应 (eABR) 的阈值在失聪 3 周时显著升高,用 GDNF 稳定,用 GDNF 停止和用抗氧化剂或生理盐水治疗时没有变化。螺旋神经节神经元的数量因失聪而减少(失聪 3 周减少 40%,11 周减少 70%),并用 GDNF 从细胞死亡中挽救出来,在停止 GDNF 治疗 4 周后,抗氧化剂和生理盐水治疗组的神经节细胞数量没有进一步减少。失聪耳朵的局部生长因子治疗可能会防止电反应恶化,并挽救听神经细胞免于死亡;这些效果持续超过治疗期,并可能增强耳蜗植入疗法对聋人的益处。

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本文引用的文献

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Enhanced survival of spiral ganglion cells after cessation of treatment with brain-derived neurotrophic factor in deafened guinea pigs.
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