小鼠前庭传出神经元的电生理特征及急性前庭外周剥夺的调节。

IF 5.8 2区 医学 Q1 NEUROSCIENCES
Jinyu Wang, Mengfan Xu, Lei Zhang, Wenjie Liu, Siyue Wang, Liqin Wang, Ning Cong, Geng-Lin Li, Jing Wang
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引用次数: 0

摘要

脑干的前庭传出神经元向周围前庭器官提供直接的胆碱能神经支配,从而调节其感觉反应。在这项研究中,一个具有胆碱乙酰转移酶驱动的荧光标记的基因靶向小鼠模型能够将这些神经元精确定位到面神经的膝背外侧区域。急性脑干切片的全细胞膜片钳记录显示,几乎所有神经元都表现出自发动作电位放电,放电模式和后超极化动力学具有明显的异质性。发现突出的a型钾电流受乙酰胆碱和降钙素基因相关肽的差异调控。急性单侧前庭剥夺诱导双侧自发放电增强,表明对改变的感觉输入敏感。这些发现定义了前庭传出神经元的内在电生理特性和神经调节机制,为其在前庭系统的生理调节和适应性可塑性中的作用提供了机制上的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrophysiological Characterization of Murine Vestibular Efferent Neurons and Modulation by Acute Peripheral Vestibular Deprivation.

Vestibular efferent neurons in the brainstem provide direct cholinergic innervation to peripheral vestibular organs, thereby modulating their sensory responsiveness. In this study, a genetically targeted mouse model with choline acetyltransferase-driven fluorescent labeling enabled the precise localization of these neurons to the dorsolateral region of the genu of the facial nerve. Whole-cell patch-clamp recordings in acute brainstem slices revealed that virtually all neurons exhibited spontaneous action potential firing, with marked heterogeneity in discharge patterns and after-hyperpolarization kinetics. Prominent A-type potassium currents were identified and found to be differentially regulated by acetylcholine and calcitonin gene-related peptide. Acute unilateral vestibular deprivation induced a bilateral enhancement of spontaneous firing, indicating sensitivity to altered sensory input. These findings define the intrinsic electrophysiological properties and neuromodulatory mechanisms of vestibular efferent neurons, providing mechanistic insight into their roles in both physiological regulation and adaptive plasticity within the vestibular system.

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来源期刊
Neuroscience bulletin
Neuroscience bulletin NEUROSCIENCES-
CiteScore
7.20
自引率
16.10%
发文量
163
审稿时长
6-12 weeks
期刊介绍: Neuroscience Bulletin (NB), the official journal of the Chinese Neuroscience Society, is published monthly by Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) and Springer. NB aims to publish research advances in the field of neuroscience and promote exchange of scientific ideas within the community. The journal publishes original papers on various topics in neuroscience and focuses on potential disease implications on the nervous system. NB welcomes research contributions on molecular, cellular, or developmental neuroscience using multidisciplinary approaches and functional strategies. We feature full-length original articles, reviews, methods, letters to the editor, insights, and research highlights. As the official journal of the Chinese Neuroscience Society, which currently has more than 12,000 members in China, NB is devoted to facilitating communications between Chinese neuroscientists and their international colleagues. The journal is recognized as the most influential publication in neuroscience research in China.
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