Integrating brainstem and cortical functional architectures

IF 21.2 1区 医学 Q1 NEUROSCIENCES Nature neuroscience Pub Date : 2024-10-16 DOI:10.1038/s41593-024-01787-0
Justine Y. Hansen, Simone Cauzzo, Kavita Singh, María Guadalupe García-Gomar, James M. Shine, Marta Bianciardi, Bratislav Misic
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Abstract

The brainstem is a fundamental component of the central nervous system, yet it is typically excluded from in vivo human brain mapping efforts, precluding a complete understanding of how the brainstem influences cortical function. In this study, we used high-resolution 7-Tesla functional magnetic resonance imaging to derive a functional connectome encompassing cortex and 58 brainstem nuclei spanning the midbrain, pons and medulla. We identified a compact set of integrative hubs in the brainstem with widespread connectivity with cerebral cortex. Patterns of connectivity between brainstem and cerebral cortex manifest as neurophysiological oscillatory rhythms, patterns of cognitive functional specialization and the unimodal–transmodal functional hierarchy. This persistent alignment between cortical functional topographies and brainstem nuclei is shaped by the spatial arrangement of multiple neurotransmitter receptors and transporters. We replicated all findings using 3-Tesla data from the same participants. Collectively, this work demonstrates that multiple organizational features of cortical activity can be traced back to the brainstem.

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整合脑干和大脑皮层功能架构
脑干是中枢神经系统的基本组成部分,但它通常被排除在活体人脑图谱绘制工作之外,因此无法全面了解脑干如何影响大脑皮层的功能。在这项研究中,我们利用高分辨率的 7 特斯拉功能磁共振成像技术得出了一个功能连接组,其中包括大脑皮层和横跨中脑、脑桥和延髓的 58 个脑干核团。我们在脑干中发现了一组紧凑的整合枢纽,它们与大脑皮层有着广泛的连接。脑干与大脑皮层之间的连接模式表现为神经生理振荡节奏、认知功能特化模式和单模态-跨模态功能层次结构。大脑皮层功能拓扑和脑干核团之间的这种持久一致性是由多种神经递质受体和转运体的空间排列形成的。我们使用来自相同参与者的 3-Tesla 数据重复了所有发现。总之,这项工作证明了大脑皮层活动的多种组织特征可以追溯到脑干。
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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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