Nature· 2025Q1
Arousal as a universal embedding for spatiotemporal brain dynamics
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- Q1SCImago
- 2025year
Short summary
Pupil diameter, a single measure of arousal, can accurately reconstruct complex, spatiotemporal brain dynamics (neuronal calcium, metabolism, blood oxygen) in mice, suggesting arousal organizes brain-wide physiology.
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Key points
- Pupil diameter can reconstruct seconds-scale spatiotemporal dynamics of neuronal calcium, metabolism, and blood oxygen in mice.
- A time-delay embedding of pupil diameter forms a low-dimensional manifold that models these brain dynamics.
- The framework integrates diverse experimental data (behavioral, electrophysiological) into a unified generative model via shared arousal mappings.
- Spontaneous, spatially structured brain fluctuations are interpreted as expressions of a low-dimensional, organism-wide dynamical system organized by arousal.
AI-generated from the title and abstract; the full text is not read.
Abstract
Neural activity in awake organisms shows widespread, spatiotemporally diverse correlations with behavioural and physiological measurements1–4. We propose that this covariation reflects in part the structured, nonlinear dynamics of an underlying arousal-related process that organizes brain-wide and body-wide physiology on the timescale of seconds. By framing this interpretation within dynamical systems theory, we arrive at a surprising prediction: a single, scalar measurement of arousal (for example, pupil diameter) should suffice to reconstruct the continuous evolution of multidimensional, spatiotemporal measurements of large-scale brain physiology. Here, to test this hypothesis, we perform multimodal cortex-wide optical imaging5 and behavioural monitoring in awake mice. We demonstrate that the seconds-scale spatiotemporal dynamics of neuronal calcium, metabolism and brain blood oxygen can be accurately and parsimoniously modelled from a low-dimensional, nonlinear manifold reconstructed from a time delay embedding6,7 of pupil diameter. Extending this framework to behavioural and electrophysiological measurements from the Allen Brain Observatory8, we demonstrate the ability to integrate diverse experimental data into a unified generative model via mappings from a shared arousal manifold. Our results support the hypothesis9 that spontaneous, spatially structured fluctuations in brain-wide physiology on timescales of seconds—widely interpreted to reflect regionally specific neural communication10,11—are in large part expressions of a low-dimensional, organism-wide dynamical system. In turn, reframing arousal itself as a latent dynamical system offers a new perspective on fluctuations in brain, body and behaviour observed across modalities, contexts and scales. Reframing of arousal as a latent dynamical system can reconstruct multidimensional measurements of large-scale spatiotemporal brain dynamics on the timescale of seconds in mice.
The authors' abstract, as published at the source. Nature, 2025 · DOI ↗
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Field: Cognitive Neuroscience
Cognitive NeuroscienceNeuroscience