Amitriptyline protects afferent synapses in the cochlea against excitotoxic trauma in vitro

Liqin Wang, Mengfan Xu, Qing Zhang, Geng-Lin Li
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Abstract

Afferent synapses between inner hair cells (IHCs) and the type I spiral ganglion neurons (SGNs) in the cochlea provide over 95% of sensory signals for auditory perception in the brain. However, these afferent synapses are particularly vulnerable to damage, for example from excitotoxicity, and exposure to noise in the environment which often leads to noise-induced cochlear synaptopathy (NICS). In this study, we simulated excitotoxic trauma by incubating kainic acid, a non-desensitizing agonist for AMPA type glutamate receptors on cultured cochleae. The possible protective effects of amitriptyline against NICS were examined. We found that, in IHCs, amitriptyline reversed the decrease of Ca2+ current and exocytosis caused by excitotoxic trauma. In SGNs, amitriptyline promoted the recovery of neurite loss caused by excitotoxic trauma. Furthermore, we found that the protective effects of amitriptyline are likely mediated by suppressing apoptosis factors that were upregulated during excitotoxic trauma. In conclusion, our results suggest that amitriptyline could protect afferent synapses in the cochlea from NICS, making it a potential drug candidate for hearing protection.

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阿米替林在体外保护耳蜗中的传入突触免受兴奋毒性创伤。
耳蜗中内毛细胞(IHC)和 I 型螺旋神经节神经元(SGN)之间的传入突触为大脑的听觉感知提供了 95% 以上的感觉信号。然而,这些传入突触特别容易受到损伤,例如兴奋毒性和暴露于环境噪音中,这通常会导致噪音诱发的耳蜗突触病(NICS)。在这项研究中,我们通过在培养耳蜗上培养凯尼酸(一种 AMPA 型谷氨酸受体的非脱敏激动剂)来模拟兴奋性毒性创伤。我们还研究了阿米替林对 NICS 可能产生的保护作用。我们发现,在 IHC 中,阿米替林逆转了兴奋性毒性创伤引起的 Ca2+ 电流和外泌的减少。在 SGNs 中,阿米替林促进了兴奋性毒性创伤导致的神经元损失的恢复。此外,我们还发现,阿米替林的保护作用可能是通过抑制兴奋性毒性创伤期间上调的凋亡因子介导的。总之,我们的研究结果表明,阿米替林可以保护耳蜗中的传入突触免受非特异性神经损伤,使其成为保护听力的潜在候选药物。
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