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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Synaptic Reorganization Response in the Cochlear Nucleus Following Intense Noise Exposure
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Synaptic Reorganization Response in the Cochlear Nucleus Following Intense Noise Exposure

机译:强噪声暴露后耳蜗核中的突触重组响应

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The cochlear nucleus, located in the brainstem, receives its afferent auditory input exclusively from the auditory nerve fibers of the ipsilateral cochlea. Noise-induced neurodegenerative changes occurring in the auditory nerve stimulate a cascade of neuroplastic changes in the cochlear nucleus resulting in major changes in synaptic structure and function. To identify some of the key molecular mechanisms mediating this synaptic reorganization, we unilaterally exposed rats to a high-intensity noise that caused significant hearing loss and then measured the resulting changes in a synaptic plasticity gene array targeting neurogenesis and synaptic reorganization. We compared the gene expression patterns in the dorsal cochlear nucleus (DCN) and ventral cochlear nucleus (VCN) on the noise-exposed side versus the unexposed side using a PCR gene array at 2 d (early) and 28 d (late) post-exposure. We discovered a number of differentially expressed genes, particularly those related to synaptogenesis and regeneration. Significant gene expression changes occurred more frequently in the VCN than the DCN and more changes were seen at 28 d versus 2 d post-exposure. We confirmed the PCR findings by in situ hybridization for Brain-derived neurotrophic factor (Bdnf), Homer-1, as well as the glutamate NMDA receptor Grin1, all involved in neurogenesis and plasticity. These results suggest that Bdnf, Homer-1 and Grin1 play important roles in synaptic remodeling and homeostasis in the cochlear nucleus following severe noise-induced afferent degeneration. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:位于脑干中的耳蜗核,专门从Ipsilidal Cochlea的听觉神经纤维接收其传入听觉输入。在听觉神经中发生的噪声诱导的神经变性变化刺激了耳蜗核中的神经塑性变化的级联导致突触结构和功能的主要变化。为了鉴定介导该突触重组的一些关键分子机制,我们单侧暴露于引起显着听力损失的高强度噪声,然后测量突触塑性基因阵列靶向神经发生和突触重组的结果。我们将背面耳蜗(DCN)和腹侧耳蜗核(VCN)的基因表达模式与在2D(早)和28d(晚)后的PCR基因阵列上与未曝光侧对未曝光侧的基因表达模式与未曝光侧进行比较。暴露。我们发现了许多差异表达的基因,特别是与突触和再生有关的基因。在VCN中比DCN更频繁地发生显着的基因表达变化,并且在28 d与2 d后,在28 d后看到更多的变化。我们通过对脑衍生的神经营养因子(BDNF),Homer-1以及谷氨酸NMDA受体Grin1的原位杂交来证实了PCR结果,也涉及神经发生和可塑性。这些结果表明,BDNF,Homer-1和Grin1在严重噪声诱导的传入退化后耳蜗细胞核中的突触重塑和稳态中起重要作用。 (c)2018年IBRO。 elsevier有限公司出版。保留所有权利。

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