听力学
听力损失
噪声性听力损失
神经突
毛细胞
神经科学
内耳
带状突触
耳蜗
感音神经性聋
科尔蒂器官
感觉系统
耳毒性
噪声暴露
医学
生物
体外
内科学
生物化学
小泡
顺铂
化疗
膜
突触小泡
作者
Hans Rommelspacher,Sujoy Bera,Benedikt Brommer,Rachael Ward,Monika Kwiatkowska,Tomasz Zygmunt,Florian Theden,Berk Üsekes,Neriman Eren,Michael Nieratschker,Christoph Arnoldner,Stefan K. Plontke,Julian Hellmann‐Regen,Reimar Schlingensiepen
标识
DOI:10.1073/pnas.2314763121
摘要
Although sudden sensorineural hearing loss (SSNHL) is a serious condition, there are currently no approved drugs for its treatment. Nevertheless, there is a growing understanding that the cochlear pathologies that underlie SSNHL include apoptotic death of sensory outer hair cells (OHCs) as well as loss of ribbon synapses connecting sensory inner hair cells (IHCs) and neurites of the auditory nerve, designated synaptopathy. Noise-induced hearing loss (NIHL) is a common subtype of SSNHL and is widely used to model hearing loss preclinically. Here, we demonstrate that a single interventive application of a small pyridoindole molecule (AC102) into the middle ear restored auditory function almost to prenoise levels in a guinea pig model of NIHL. AC102 prevented noise-triggered loss of OHCs and reduced IHC synaptopathy suggesting a role of AC102 in reconnecting auditory neurons to their sensory target cells. Notably, AC102 exerted its therapeutic properties over a wide frequency range. Such strong improvements in hearing have not previously been demonstrated for other therapeutic agents. In vitro experiments of a neuronal damage model revealed that AC102 protected cells from apoptosis and promoted neurite growth. These effects may be explained by increased production of adenosine triphosphate, indicating improved mitochondrial function, and reduced levels of reactive-oxygen species which prevents the apoptotic processes responsible for OHC death. This action profile of AC102 might be causal for the observed hearing recovery in in vivo models.
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