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传出神经对外耳声损伤的保护作用是通过外毛细胞上的α9烟碱型乙酰胆碱受体介导的。

Efferent protection from acoustic injury is mediated via alpha9 nicotinic acetylcholine receptors on outer hair cells.

作者信息

Maison Stephane F, Luebke Anne E, Liberman M Charles, Zuo Jian

机构信息

Department of Otology and Laryngology, Harvard Medical School and Eaton-Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114-3096, USA.

出版信息

J Neurosci. 2002 Dec 15;22(24):10838-46. doi: 10.1523/JNEUROSCI.22-24-10838.2002.

Abstract

Exposure to intense sound can damage the mechanosensors of the inner ear and their afferent innervation. These neurosensory elements are innervated by a sound-activated feedback pathway, the olivocochlear efferent system. One major component of this system is cholinergic, and known cholinergic effects are mediated by the alpha9/alpha10 nicotinic acetylcholine receptor (nAChR) complex. Here, we show that overexpression of alpha9 nAChR in the outer hair cells of bacterial artificial chromosome transgenic mice significantly reduces acoustic injury from exposures causing either temporary or permanent damage, without changing pre-exposure cochlear sensitivity to low- or moderate-level sound. These data demonstrate that efferent protection is mediated via the alpha9 nAChR in the outer hair cells and provide direct evidence for a protective role, in vivo, of a member of the nAChR family.

摘要

暴露于高强度声音会损害内耳的机械传感器及其传入神经支配。这些神经感觉元件由声音激活的反馈通路——橄榄耳蜗传出系统支配。该系统的一个主要成分是胆碱能的,已知的胆碱能效应由α9/α10烟碱型乙酰胆碱受体(nAChR)复合物介导。在这里,我们表明,在细菌人工染色体转基因小鼠的外毛细胞中过表达α9 nAChR可显著降低由导致暂时或永久性损伤的暴露所引起的声学损伤,而不会改变暴露前耳蜗对低或中等强度声音的敏感性。这些数据表明,传出保护是通过外毛细胞中的α9 nAChR介导的,并为nAChR家族成员在体内的保护作用提供了直接证据。

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