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Oxygen and the Spark of Human Brain Evolution: Complex Interactions of Metabolism and Cortical Expansion across Development and Evolution.
Luppi, Andrea I; Rosas, Fernando E; Noonan, MaryAnn P; Mediano, Pedro A M; Kringelbach, Morten L; Carhart-Harris, Robin L; Stamatakis, Emmanuel A; Vernon, Anthony C; Turkheimer, Federico E.
Afiliação
  • Luppi AI; Department of Clinical Neurosciences and Division of Anaesthesia, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Rosas FE; Leverhulme Centre for the Future of Intelligence, University of Cambridge, Cambridge, UK.
  • Noonan MP; The Alan Turing Institute, London, UK.
  • Mediano PAM; Department of Informatics, University of Sussex, Brighton, UK.
  • Kringelbach ML; Centre for Psychedelic Research, Department of Brain Science, Imperial College London, London, UK.
  • Carhart-Harris RL; Centre for Complexity Science, Imperial College London, London, UK.
  • Stamatakis EA; Centre for Eudaimonia and Human Flourishing, University of Oxford, Oxford, UK.
  • Vernon AC; Department of Experimental Psychology, University of Oxford, Oxford, UK.
  • Turkheimer FE; Department of Psychology, University of Cambridge, Cambridge, UK.
Neuroscientist ; : 10738584221138032, 2022 Dec 08.
Article em En | MEDLINE | ID: mdl-36476177
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article