Department of Otorhinolaryngology and Head & Neck Surgery, University Medical Center Utrecht, Utrecht University, Room G.02.531, P.O. Box 85500, 3508 GA, Utrecht, the Netherlands; UMC Utrecht Brain Center, Utrecht University, the Netherlands.
Hear Res. 2020 May;390:107928. doi: 10.1016/j.heares.2020.107928. Epub 2020 Feb 24.
Severe damage to the organ of Corti leads to degeneration of the spiral ganglion cells (SGCs) which form the auditory nerve. This degeneration starts at the level of synaptic connection of the peripheral processes (PPs) of SGCs with the cochlear hair cells. It is generally thought that from this point SGC degeneration progresses in a retrograde fashion: PPs degenerate first, followed by the SGC soma with a delay of several weeks to many months. Evidence for this course of events, both in animals and in humans, is not unambiguous, while this knowledge is important since the presence or absence of the different neural elements may greatly influence the response to electrical stimulation with a cochlear implant (CI). We therefore aimed to provide a comprehensive account of the course of SGC degeneration in the guinea pig cochlea after ototoxic treatment. Histological analysis of eighteen healthy and thirty-three deafened cochleas showed that the degeneration of SGCs and their peripheral processes was simultaneous rather than sequential. As the site of excitation for electrical stimulation with a CI may depend on the course of degeneration of the various neural elements, this finding is relevant both for understanding the electrophysiological mechanisms behind cochlear implantation and for recent efforts to induce PP resprouting for improved electrode-neural interface. Since excitation of the PPs is often thought to result in (secondary) longer-latency activity, we tested the hypothesis that having relatively many PPs produces a larger N peak in the electrically evoked compound action potential (eCAP); the present findings however do not support this theory. The course of the degeneration process may vary among species, and may depend on the cause of deafness, but the present findings at least indicate that gradual retrograde degeneration of the auditory nerve is not an elemental process following severe damage to the organ of Corti.
严重的柯蒂氏器损伤会导致螺旋神经节细胞(SGC)的退化,而 SGC 则形成听觉神经。这种退化始于 SGC 外周突(PP)与耳蜗毛细胞突触连接水平。一般认为,从这一点开始,SGC 退化呈逆行方式进行:PP 首先退化,随后 SGC 体部延迟数周至数月退化。无论是在动物还是在人类中,这一事件进程的证据都不是明确的,而这一知识非常重要,因为不同神经元件的存在或缺失可能会极大地影响耳蜗植入(CI)的电刺激反应。因此,我们旨在全面描述豚鼠耳蜗在耳毒性治疗后的 SGC 退化过程。对 18 个健康和 33 个失聪耳蜗的组织学分析表明,SGC 及其外周突的退化是同时发生的,而不是顺序发生的。由于 CI 电刺激的激发部位可能取决于各种神经元件的退化过程,因此这一发现不仅与理解耳蜗植入背后的电生理机制有关,而且与最近为改善电极-神经界面而进行的刺激 PP 再生的努力有关。由于 PP 的兴奋通常被认为会导致(次级)更长潜伏期的活动,我们测试了这样一个假设,即具有相对较多的 PP 会在电诱发复合动作电位(eCAP)中产生更大的 N 峰;然而,目前的发现并不支持这一理论。退化过程的进程可能因物种而异,也可能取决于耳聋的原因,但目前的发现至少表明,严重的柯蒂氏器损伤后,听觉神经的逐渐逆行退化不是一个基本过程。