脑切片全细胞膜片钳记录双侧下丘相互作用调控神经元潜伏期的研究。

IF 3 4区 医学 Q2 NEUROSCIENCES
Neural Plasticity Pub Date : 2021-12-10 eCollection Date: 2021-01-01 DOI:10.1155/2021/8030870
Jinzhe Ma, Yangyang Han, Yiting Yao, Huimei Wang, Mengxia Chen, Ziying Fu, Qicai Chen, Jia Tang
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引用次数: 0

摘要

下丘作为皮质下核中双耳整合中枢的最后一级,在接收双耳信息输入中起着至关重要的作用。以往的研究主要集中在双侧IC之间的相互作用如何影响IC神经元的放电速率。然而,关于双侧IC内的相互作用如何影响神经元潜伏期,我们知之甚少。在本研究中,我们探讨了双侧IC相互作用对IC神经元潜伏期影响的突触机制。我们使用全细胞膜片钳记录来评估昆明小鼠离体脑切片的突触反应。结果表明,双侧IC之间以兴奋-抑制投射为主,双侧IC相互作用可不同程度地改变大多数神经元的反应潜伏期。潜伏期的变化与突触输入的类型、兴奋和抑制的相对强度有关。此外,潜伏期的变化还与神经元第一次阈下去极化放电反应的持续时间变化有关。不同类型的突触输入的分布特征也不同。兴奋抑制性神经元广泛分布于IC背核和中央核,而兴奋性神经元则相对集中于这两个核。由于被测神经元数量少,抑制神经元没有明显的分布趋势。这些结果为揭示双侧IC投射的调节功能提供了实验参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Investigation of Neuron Latency Modulated by Bilateral Inferior Collicular Interactions Using Whole-Cell Patch Clamp Recording in Brain Slices.

Investigation of Neuron Latency Modulated by Bilateral Inferior Collicular Interactions Using Whole-Cell Patch Clamp Recording in Brain Slices.

Investigation of Neuron Latency Modulated by Bilateral Inferior Collicular Interactions Using Whole-Cell Patch Clamp Recording in Brain Slices.

Investigation of Neuron Latency Modulated by Bilateral Inferior Collicular Interactions Using Whole-Cell Patch Clamp Recording in Brain Slices.

As the final level of the binaural integration center in the subcortical nucleus, the inferior colliculus (IC) plays an essential role in receiving binaural information input. Previous studies have focused on how interactions between the bilateral IC affect the firing rate of IC neurons. However, little is known concerning how the interactions within the bilateral IC affect neuron latency. In this study, we explored the synaptic mechanism of the effect of bilateral IC interactions on the latency of IC neurons. We used whole-cell patch clamp recordings to assess synaptic responses in isolated brain slices of Kunming mice. The results demonstrated that the excitation-inhibition projection was the main projection between the bilateral IC. Also, the bilateral IC interactions could change the reaction latency of most neurons to different degrees. The variation in latency was related to the type of synaptic input and the relative intensity of the excitation and inhibition. Furthermore, the latency variation also was caused by the duration change of the first subthreshold depolarization firing response of the neurons. The distribution characteristics of the different types of synaptic input also differed. Excitatory-inhibitory neurons were widely distributed in the IC dorsal and central nuclei, while excitatory neurons were relatively concentrated in these two nuclei. Inhibitory neurons did not exhibit any apparent distribution trend due to the small number of assessed neurons. These results provided an experimental reference to reveal the modulatory functions of bilateral IC projections.

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来源期刊
Neural Plasticity
Neural Plasticity NEUROSCIENCES-
CiteScore
6.80
自引率
0.00%
发文量
77
审稿时长
16 weeks
期刊介绍: Neural Plasticity is an international, interdisciplinary journal dedicated to the publication of articles related to all aspects of neural plasticity, with special emphasis on its functional significance as reflected in behavior and in psychopathology. Neural Plasticity publishes research and review articles from the entire range of relevant disciplines, including basic neuroscience, behavioral neuroscience, cognitive neuroscience, biological psychology, and biological psychiatry.
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