下丘脑-后脑回路中的一小部分应激反应神经元介导了小鼠抑郁样行为的发展。

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-10-03 DOI:10.1016/j.neuron.2024.09.012
Zhiwei Zheng, Yiqin Liu, Ruiqi Mu, Xiaonan Guo, Yirong Feng, Chen Guo, Liang Yang, Wenxi Qiu, Qi Zhang, Wei Yang, Zhaoqi Dong, Shuang Qiu, Yiyan Dong, Yihui Cui
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引用次数: 0

摘要

越来越多的证据表明,各种大脑功能都与经验激活的神经元组合有关。然而,这种神经元组合是否参与了压力诱发抑郁症的发病机制仍未确定。利用小鼠活动依赖性病毒策略,我们发现了一小部分应激反应神经元,它们主要位于下丘脑外侧中部(mLH)和外侧哈文脑内侧(LHbM)。这些神经元作为 "启动细胞 "传递与压力相关的信息,并在慢性压力下介导抑郁样行为的发生。mLH 和 LHbM 中的启动细胞会形成优势连接,慢性应激会选择性地增强这些连接。在慢性应激过程中沉默这些连接可防止抑郁样行为的发生,而激活这些连接则会在没有应激经历的情况下直接诱发抑郁样行为。总之,我们的研究结果剖析了LH-LHb回路中介导小鼠抑郁样行为发生的核心功能单元。
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A small population of stress-responsive neurons in the hypothalamus-habenula circuit mediates development of depression-like behavior in mice.

Accumulating evidence has shown that various brain functions are associated with experience-activated neuronal ensembles. However, whether such neuronal ensembles are engaged in the pathogenesis of stress-induced depression remains elusive. Utilizing activity-dependent viral strategies in mice, we identified a small population of stress-responsive neurons, primarily located in the middle part of the lateral hypothalamus (mLH) and the medial part of the lateral habenula (LHbM). These neurons serve as "starter cells" to transmit stress-related information and mediate the development of depression-like behaviors during chronic stress. Starter cells in the mLH and LHbM form dominant connections, which are selectively potentiated by chronic stress. Silencing these connections during chronic stress prevents the development of depression-like behaviors, whereas activating these connections directly elicits depression-like behaviors without stress experience. Collectively, our findings dissect a core functional unit within the LH-LHb circuit that mediates the development of depression-like behaviors in mice.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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