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联合胶质细胞源性神经营养因子延迟治疗与持续电刺激对耳聋豚鼠螺旋神经节细胞存活的影响

Effects of delayed treatment with combined GDNF and continuous electrical stimulation on spiral ganglion cell survival in deafened guinea pigs.

作者信息

Scheper Verena, Paasche Gerrit, Miller Josef M, Warnecke Athanasia, Berkingali Nurdanat, Lenarz Thomas, Stöver Timo

机构信息

Department of Otolaryngology, Medical University Hannover, Hannover, Germany.

出版信息

J Neurosci Res. 2009 May 1;87(6):1389-99. doi: 10.1002/jnr.21964.

Abstract

Electrical stimulation (ES) of spiral ganglion cells (SGC) via a cochlear implant is the standard treatment for profound sensor neural hearing loss. However, loss of hair cells as the morphological correlate of sensor neural hearing loss leads to deafferentation and death of SGC. Although immediate treatment with ES or glial cell line-derived neurotrophic factor (GDNF) can prevent degeneration of SGC, only few studies address the effectiveness of delayed treatment. We hypothesize that both interventions have a synergistic effect and that even delayed treatment would protect SGC. Therefore, an electrode connected to a pump was implanted into the left cochlea of guinea pigs 3 weeks after deafening. The contralateral untreated cochleae served as deafened intraindividual controls. Four groups were set up. Control animals received intracochlear infusion of artificial perilymph (AP/-). The experimental groups consisted of animals treated with AP in addition to continuous ES (AP/ES) or treated with GDNF alone (GDNF/-) or GDNF combined with continuous ES (GDNF/ES). Acoustically and electrically evoked auditory brain stem responses were recorded. All animals were killed 48 days after deafening; their cochleae were histologically evaluated. Survival of SGC increased significantly in the GDNF/- and AP/ES group compared with the AP/- group. A highly significant increase in SGC density was observed in the GDNF/ES group compared with the control group. Additionally, animals in the GDNF/ES group showed reduced EABR thresholds. Thus, delayed treatment with GDNF and ES can protect SGC from degeneration and may improve the benefits of cochlear implants.

摘要

通过人工耳蜗对螺旋神经节细胞(SGC)进行电刺激(ES)是重度感音神经性听力损失的标准治疗方法。然而,作为感音神经性听力损失形态学关联的毛细胞丧失会导致SGC的去传入和死亡。尽管立即使用ES或胶质细胞源性神经营养因子(GDNF)进行治疗可以防止SGC变性,但只有少数研究探讨了延迟治疗的有效性。我们假设这两种干预措施具有协同作用,并且即使是延迟治疗也能保护SGC。因此,在致聋3周后,将连接到泵的电极植入豚鼠的左耳蜗。对侧未经治疗的耳蜗作为个体内致聋对照。设立了四组。对照动物接受人工外淋巴(AP/-)的耳蜗内输注。实验组包括除连续ES外还接受AP治疗的动物(AP/ES)、单独接受GDNF治疗的动物(GDNF/-)或GDNF与连续ES联合治疗的动物(GDNF/ES)。记录听觉和电诱发的听觉脑干反应。所有动物在致聋48天后处死;对其耳蜗进行组织学评估。与AP/-组相比,GDNF/-组和AP/ES组的SGC存活率显著增加。与对照组相比,GDNF/ES组的SGC密度显著增加。此外,GDNF/ES组的动物显示出EABR阈值降低。因此,GDNF和ES的延迟治疗可以保护SGC免于变性,并可能改善人工耳蜗的益处。

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