Evidence map›Paper›PMID 36476177›Full record

ArticleThe Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry2024

Oxygen and the Spark of Human Brain Evolution: Complex Interactions of Metabolism and Cortical Expansion across Development and Evolution.

Andrea I Luppi, Fernando E Rosas, MaryAnn P Noonan, Pedro A M Mediano, Morten L Kringelbach, Robin L Carhart-Harris, Emmanuel A Stamatakis, Anthony C Vernon, Federico E Turkheimer

Abstract read
In one paragraph

Article in The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. The control costs of human brain dynamics.Network neuroscience (Cambridge, Mass.) · 2025
    Article
  4. Article
  5. The evolutionary origins of dementia.Journal of Alzheimer's disease reports
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Andrea I LuppiDepartment of Clinical Neurosciences and Division of Anaesthesia, School of Clinical Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0002-3461-6431
Fernando E RosasDepartment of Informatics, University of Sussex, Brighton, UK.
MaryAnn P NoonanDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Pedro A M MedianoDepartment of Psychology, University of Cambridge, Cambridge, UK.
Morten L KringelbachCentre for Eudaimonia and Human Flourishing, University of Oxford, Oxford, UK.
Robin L Carhart-HarrisPsychedelics Division-Neuroscape, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
Emmanuel A StamatakisDepartment of Clinical Neurosciences and Division of Anaesthesia, School of Clinical Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0001-6955-9601
Anthony C VernonMRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Federico E TurkheimerDepartment of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0002-3766-3815

Funding

Medical Research Council MR/W006251/1Wellcome Trust
6 · The paper itself

Abstract

Scientific theories on the functioning and dysfunction of the human brain require an understanding of its development-before and after birth and through maturation to adulthood-and its evolution. Here we bring together several accounts of human brain evolution by focusing on the central role of oxygen and brain metabolism. We argue that evolutionary expansion of human transmodal association cortices exceeded the capacity of oxygen delivery by the vascular system, which led these brain tissues to rely on nonoxidative glycolysis for additional energy supply. We draw a link between the resulting lower oxygen tension and its effect on cytoarchitecture, which we posit as a key driver of genetic developmental programs for the human brain-favoring lower intracortical myelination and the presence of biosynthetic materials for synapse turnover. Across biological and temporal scales, this protracted capacity for neural plasticity sets the conditions for cognitive flexibility and ongoing learning, supporting complex group dynamics and intergenerational learning that in turn enabled improved nutrition to fuel the metabolic costs of further cortical expansion. Our proposed model delineates explicit mechanistic links among metabolism, molecular and cellular brain heterogeneity, and behavior, which may lead toward a clearer understanding of brain development and its disorders.

Indexed as

BrainOxygenBiological EvolutionCerebral CortexHumansLearningLongitudinal StudiesOxygenaerobic glycolysiscomplex systemscortical expansiondevelopmentevolutionmetabolismoxygenplasticitysocial braintransmodal association cortex

Identifiers

PMID36476177
PMCPMC10928962

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.