Tonic and burst-like locus coeruleus stimulation distinctly shift network activity across the cortical hierarchy

IF 21.2 1区 医学 Q1 NEUROSCIENCES Nature neuroscience Pub Date : 2024-09-16 DOI:10.1038/s41593-024-01755-8
Christina Grimm, Sian N. Duss, Mattia Privitera, Brandon R. Munn, Nikolaos Karalis, Stefan Frässle, Maria Wilhelm, Tommaso Patriarchi, Daniel Razansky, Nicole Wenderoth, James M. Shine, Johannes Bohacek, Valerio Zerbi
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Abstract

Noradrenaline (NA) release from the locus coeruleus (LC) changes activity and connectivity in neuronal networks across the brain, modulating multiple behavioral states. NA release is mediated by both tonic and burst-like LC activity. However, it is unknown whether the functional changes in target areas depend on these firing patterns. Using optogenetics, photometry, electrophysiology and functional magnetic resonance imaging in mice, we show that tonic and burst-like LC firing patterns elicit brain responses that hinge on their distinct NA release dynamics. During moderate tonic LC activation, NA release engages regions associated with associative processing, while burst-like stimulation biases the brain toward sensory processing. These activation patterns locally couple with increased astrocytic and inhibitory activity and change the brain’s topological configuration in line with the hierarchical organization of the cerebral cortex. Together, these findings reveal how the LC–NA system achieves a nuanced regulation of global circuit operations.

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节律性和猝发样刺激可明显改变整个大脑皮层的网络活动
去甲肾上腺素(NA)从脑小叶位置(LC)释放,会改变整个大脑神经元网络的活动和连接,从而调节多种行为状态。NA的释放是由LC的强直性和爆发性活动介导的。然而,目标区域的功能变化是否取决于这些发射模式尚不得而知。通过在小鼠体内使用光遗传学、光度计、电生理学和功能磁共振成像技术,我们发现强直性和爆发样 LC 发射模式会引起大脑反应,而这些反应取决于它们不同的 NA 释放动态。在适度的强直性 LC 激活过程中,NA 的释放涉及与联想处理相关的区域,而爆发式刺激则使大脑偏向于感觉处理。这些激活模式在局部与增加的星形胶质细胞和抑制性活动相结合,改变了大脑的拓扑结构,使其与大脑皮层的分层组织相一致。这些发现共同揭示了 LC-NA 系统如何实现对全局电路运行的细微调节。
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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