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

Author:

Luppi Andrea I.123ORCID,Rosas Fernando E.4567,Noonan MaryAnn P.8,Mediano Pedro A. M.91011,Kringelbach Morten L.71213,Carhart-Harris Robin L.14,Stamatakis Emmanuel A.1ORCID,Vernon Anthony C.1516,Turkheimer Federico E.17ORCID

Affiliation:

1. Department of Clinical Neurosciences and Division of Anaesthesia, School of Clinical Medicine, University of Cambridge, Cambridge, UK

2. Leverhulme Centre for the Future of Intelligence, University of Cambridge, Cambridge, UK

3. The Alan Turing Institute, London, UK

4. Department of Informatics, University of Sussex, Brighton, UK

5. Centre for Psychedelic Research, Department of Brain Science, Imperial College London, London, UK

6. Centre for Complexity Science, Imperial College London, London, UK

7. Centre for Eudaimonia and Human Flourishing, University of Oxford, Oxford, UK

8. Department of Experimental Psychology, University of Oxford, Oxford, UK

9. Department of Psychology, University of Cambridge, Cambridge, UK

10. Department of Psychology, Queen Mary University of London, London, UK

11. Department of Computing, Imperial College London, London, UK

12. Center for Music in the Brain, Aarhus University, Aarhus, Denmark

13. Department of Psychiatry, University of Oxford, Oxford, UK

14. Psychedelics Division–Neuroscape, Department of Neurology, University of California San Francisco, San Francisco, CA, USA

15. MRC Centre for Neurodevelopmental Disorders, King’s College London, London, UK

16. Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK

17. Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK

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.

Funder

Wellcome

Canadian Institute for Advanced Research

Medical Research Council

Gates Cambridge Trust

Queens College Cambridge

Ad Astra Chandaria Foundation

Danmarks Grundforskningsfond

Carlsbergfondet

National Institute for Health Research

King’s College London

Publisher

SAGE Publications

Subject

Neurology (clinical),General Neuroscience

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