Human brain dynamics are shaped by rare long-range connections over and above cortical geometry

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Jakub Vohryzek, Yonatan Sanz-Perl, Morten L. Kringelbach, Gustavo Deco
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Abstract

A fundamental topological principle is that the container always shapes the content. In neuroscience, this translates into how the brain anatomy shapes brain dynamics. From neuroanatomy, the topology of the mammalian brain can be approximated by local connectivity, accurately described by an exponential distance rule (EDR). The compact, folded geometry of the cortex is shaped by this local connectivity, and the geometric harmonic modes can reconstruct much of the functional dynamics. However, this ignores the fundamental role of the rare long-range (LR) cortical connections, crucial for improving information processing in the mammalian brain, but not captured by local cortical folding and geometry. Here, we show the superiority of harmonic modes combining rare LR connectivity with EDR (EDR+LR) in capturing functional dynamics (specifically LR functional connectivity and task-evoked brain activity) compared to geometry and EDR representations. Importantly, the orchestration of dynamics is carried out by a more efficient manifold made up of a low number of fundamental EDR+LR modes. Our results show the importance of rare LR connectivity for capturing the complexity of functional brain activity through a low-dimensional manifold shaped by fundamental EDR+LR modes.
人类大脑的动态是由皮质几何结构之上的罕见的远程连接形成的
一个基本的拓扑原则是容器总是塑造内容。在神经科学中,这转化为大脑解剖学如何塑造大脑动力学。从神经解剖学来看,哺乳动物大脑的拓扑结构可以用局部连接来近似,用指数距离规则(EDR)精确地描述。皮质的紧凑、折叠的几何形状是由这种局部连接形成的,几何谐波模式可以重建许多功能动态。然而,这忽略了罕见的远程(LR)皮层连接的基本作用,这种连接对于改善哺乳动物大脑的信息处理至关重要,但却没有被局部皮层折叠和几何捕获。在这里,我们展示了谐波模式结合罕见的LR连接与EDR (EDR+LR)在捕获功能动态(特别是LR功能连接和任务诱发的大脑活动)方面的优势,而不是几何和EDR表征。重要的是,动态的编排是由一个更有效的流形组成的低数量的基本EDR+LR模式。我们的研究结果表明,罕见的LR连接对于通过基本EDR+LR模式形成的低维流形捕捉功能性大脑活动的复杂性具有重要意义。
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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