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Nature Neuroscience· 2026Q1

Comprehensive profiling of brain dynamics during anesthesia across phylogeny

Andrea I. Luppi, Lynn Uhrig, Jordy Tasserie, Golia Shafiei et al.

Short summary

Anesthesia induces a conserved neural state across species, characterized by shorter intrinsic timescales and reduced inter-regional synchrony, which can be reversed by deep-brain stimulation.

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Key points

  • Anesthesia induces a conserved dynamical profile across species, including humans, macaques, mice, zebrafish, and nematodes.
  • This conserved profile is marked by shorter intrinsic timescales of neural activity and dampened inter-regional synchrony.
  • Deep-brain stimulation of the macaque centromedian thalamus reversed these neural changes and restored behavioral responsiveness.
  • The neural phenotype correlates with conserved transcriptional profiles of neurotransmission and is mechanistically linked to molecular targets affecting synaptic timescales.

AI-generated from the title and abstract; the full text is not read.

Abstract

The behavioral effects of anesthetics are highly conserved across species, hinting at shared and fundamental underlying mechanisms. Here we compile a dataset of multiscale neural activity during wakefulness and anesthesia, encompassing human, macaque, marmoset, mouse, zebrafish and nematode. Applying massive feature extraction, we characterize local neural dynamics across >6,000 time-series features. This reveals a conserved dynamical profile of anesthesia across species, characterized by shorter intrinsic timescales of neural activity and dampened inter-regional synchrony. Deep-brain stimulation of the macaque centromedian thalamus reverses this profile and restores behavioral responsiveness. This conserved dynamical phenotype covaries with conserved transcriptional profiles of excitatory and inhibitory neurotransmission. Biophysical modeling provides a potential mechanistic link between the macroscale dynamical phenotype of anesthesia and microscale effects of key molecular targets on the timescales of synaptic excitation and inhibition. These analyses reveal a shared neural endpoint of anesthesia: across species and scales, anesthetics induce spatiotemporal isolation of local neural activity.

The authors' abstract, as published at the source. Nature Neuroscience, 2026 · DOI ↗

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Field: Cognitive Neuroscience

Cognitive NeuroscienceNeuroscience