应激时外侧哈文脑活动增强会产生易感性的全脑和行为基础。

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Anna Zhukovskaya, Christopher A Zimmerman, Lindsay Willmore, Alejandro Pan-Vazquez, Sanjeev R Janarthanan, Laura A Lynch, Annegret L Falkner, Ilana B Witten
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引用次数: 0

摘要

有些人容易受到慢性压力的影响,而有些人则更有韧性。虽然许多与学习有关的脑区在应激后会失调,但人们对易受应激影响的个体和抗应激能力强的个体在应激期间的神经教学信号是否存在差异以及如何差异知之甚少。在这里,我们试图确定编码消极教学信号的外侧脑叶(LHb)的活动是否在易受应激影响的小鼠和具有抗应激能力的小鼠之间存在差异,从而产生不同的结果。在慢性社会挫败应激之后(而非之前),当易感小鼠靠近攻击性品系时,LHb会活跃。在应激过程中,易感小鼠在与攻击者互动时的活性较高,并且激活会使小鼠偏向易感性。这种操作会使易感小鼠皮层下与皮层活动的平衡出现持续而广泛的增加。综上所述,我们的研究结果表明,应激时 LHb 活动的增强会产生持久的全脑和行为易感性基质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heightened lateral habenula activity during stress produces brainwide and behavioral substrates of susceptibility.

Some individuals are susceptible to chronic stress, and others are more resilient. While many brain regions implicated in learning are dysregulated after stress, little is known about whether and how neural teaching signals during stress differ between susceptible and resilient individuals. Here, we seek to determine if activity in the lateral habenula (LHb), which encodes a negative teaching signal, differs between susceptible and resilient mice during stress to produce different outcomes. After (but not before) chronic social defeat stress, the LHb is active when susceptible mice are in proximity of the aggressor strain. During stress, activity is higher in susceptible mice during aggressor interactions, and activation biases mice toward susceptibility. This manipulation generates a persistent and widespread increase in the balance of subcortical vs. cortical activity in susceptible mice. Taken together, our results indicate that heightened activity in the LHb during stress produces lasting brainwide and behavioral substrates of susceptibility.

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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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