A genetic perspective on glucose consumption in the cerebral cortex during human development

Diabetes Obes Metab. 2014 Sep:16 Suppl 1:21-5. doi: 10.1111/dom.12333.

Abstract

As the major glucose-consuming organ in the human body, the dynamics of glucose metabolism in the brain deserve special attention. It has been shown that the brain's energy allocation as a percentage of the total energy budget of the individual peaks during childhood and declines through adolescence until reaching the stable allocation level seen in the adult. This pattern of glucose consumption has not been observed in other species, including our close primate relatives, and is therefore potentially either a driver or a consequence of human cognition. Furthermore, the allocation of glucose usage in the brain changes as the individual ages, with a surprising amount dedicated to glycolysis rather than oxidative phosphorylation pathway. This suggests that, at certain developmental stages, glucose-fuelled anabolic pathways, in addition to ATP generation, are the driving forces behind the brain's high energy requirement. In this study, we explore the most recent work pertaining to the dynamic glucose uptake and allocation of the developing human brain and investigate several genes that may play a role in regulating these processes.

Keywords: Warburg effect; aerobic glycolysis; brain development; comparative development; glucose metabolism.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Aging*
  • Animals
  • Cerebral Cortex / growth & development
  • Cerebral Cortex / metabolism*
  • Energy Metabolism
  • Gene Expression Regulation, Developmental*
  • Glucose / metabolism
  • Glycolysis*
  • Humans
  • Models, Neurological*
  • Neocortex / growth & development
  • Neocortex / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurogenesis
  • Neurons / cytology
  • Neurons / metabolism*
  • Organ Specificity
  • Oxidative Phosphorylation*

Substances

  • Nerve Tissue Proteins
  • Glucose