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Neuroplasticity reflects the brain's remarkable capacity to adapt and evolve, responding dynamically to learning, experiences, or injury by reorganizing its neural circuitry. This reorganization involves creating new neural connections and refining old ones through a series of biological processes that contribute to the brain's lifelong development and adaptability.

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Related Experiment Video

Updated: Jun 20, 2026

Whole-Brain 3D Activation and Functional Connectivity Mapping in Mice using Transcranial Functional Ultrasound Imaging
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Evolutionarily conserved fMRI network dynamics in the mouse, macaque, and human brain.

Daniel Gutierrez-Barragan1, Julian S B Ramirez2, Stefano Panzeri3

  • 1Functional Neuroimaging Lab, Istituto Italiano di Tecnologia, Center for Neuroscience and Cognitive Systems, Rovereto, Italy.

Nature Communications
|October 1, 2024
PubMed
Summary
This summary is machine-generated.

Brain network dynamics are surprisingly similar across mammals. Researchers found conserved coactivation modes (C-modes) in macaques, humans, and rodents, revealing shared principles in brain organization.

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Area of Science:

  • Neuroscience
  • Comparative Biology
  • Systems Neuroscience

Background:

  • Resting-state functional magnetic resonance imaging (fMRI) studies have identified evolutionarily relevant brain networks using time-averaged analyses.
  • However, the dynamic, second-by-second evolution of fMRI network activity and its cross-species conservation remain largely unexplored.

Purpose of the Study:

  • To investigate whether the dynamic organization of resting-state fMRI network activity is conserved across mammalian species.
  • To identify common dynamic principles governing brain network organization across phylogeny.

Main Methods:

  • Applied frame-wise clustering to fMRI time-series data from awake male macaques and humans.
  • Analyzed the dynamic transitions between intrinsic fMRI coactivation modes (C-modes).
  • Compared dynamic features and neuroanatomical homology of C-modes across species, including rodents.

Main Results:

  • Identified 4 dominant, neuroanatomically homologous fMRI coactivation modes (C-modes) in macaques and humans, with 3 plausibly present in rodents.
  • Observed species-invariant dynamic features of C-modes, including preferred occurrence during specific global signal fluctuation phases and infraslow coupled oscillator dynamics.
  • Demonstrated that dominant C-mode occurrence reconstructs static fMRI connectome organization and predicts connectivity gradient rankings across species.

Conclusions:

  • Revealed a set of species-invariant principles governing the dynamic organization of fMRI networks in mammals.
  • Established a framework for relating fMRI network findings across the mammalian phylogenetic tree by focusing on dynamic organization.