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The inner hair cell afferent/efferent synapses revisited: a basis for new therapeutic strategies.

机译:内毛细胞传入/传出突触重新审视:新的治疗策略的基础。

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摘要

Within the cochlea, the sensory inner hair cells, which transduce the mechanical displacement of the basilar membrane into neural activity, release glutamate that acts on postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptor channels located on dendrites of primary auditory neurons. Up to now, it has been thought that the auditory nerve responses passively reflected the motion of the basilar membrane supporting the organ of Corti. Here, we show that dopaminergic lateral olivocochlear efferents drive a permanent gain control at the site of auditory action potential initialization. A dysfunction of this system leads to the development of early signs of excitotoxicity. With the knowledge of the molecular mechanisms involved at this first synaptic complex in the cochlea, it is now possible to envisage local treatments for spiral ganglion neurons, either to stop an excitotoxically induced hyperexcitability (probably the starting point of most posttraumatic tinnitus) or to preventneuronal death (neural presbycusis).
机译:在耳蜗内,感觉内毛细胞将基底膜的机械位移转化为神经活动,释放出谷氨酸盐,该谷氨酸作用于位于突触后的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯(AMPA)受体通道在初级听觉神经元的树突上。迄今为止,已经认为听神经反应被动地反映了支持Corti器官的基底膜的运动。在这里,我们表明,多巴胺能侧耳蜗外侧传出在听觉动作电位初始化的位置驱动一个永久的增益控制。该系统的功能障碍导致兴奋性毒性的早期迹象的发展。了解了耳蜗中第一个突触复合体所涉及的分子机制后,现在可以设想对螺旋神经节神经元进行局部治疗,以终止兴奋性中毒诱导的过度兴奋(可能是大多数创伤后耳鸣的起点)或预防神经元死亡(神经性老花眼)。

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