Changes in components of energy regulation in mouse cortex with increases in wakefulness

Sleep. 2010 Jul;33(7):889-900. doi: 10.1093/sleep/33.7.889.

Abstract

Study objectives: Increases in ATP production machinery have been described in brain after 3 h of sleep deprivation. Whether this is sustained with longer durations of extended wakefulness is unknown. We hypothesized that energy depletion could be a mechanism leading to difficulty maintaining wakefulness and assessed changes in components of the electron transport chain.

Design: Protein levels of key subunits of complexes IV and V of the electron transport chain (COXI, COXIV, ATP5B) and uncoupling protein 2 (UCP2) in isolated mitochondria by Westerns in mouse cerebral cortex after 3 and 12 h of sleep deprivation were compared to that in control mice. Activity of complex IV enzyme and relevant transcription factors-Nrf1, Nrf2 (Gabp), and phosphorylation of AMP-dependent kinase (AMPK)-were also assessed.

Participants: 8-10 week old C57BL/6J male mice (n = 91).

Interventions: 3, 6, and 12 h of sleep deprivation.

Measurements and results: After both 3 and 12 h of sleep deprivation, complex IV proteins and enzyme activity were significantly increased. The complex V catalytic subunit was significantly increased after 12 h of sleep deprivation only. Increased levels of UCP2 protein after 12 h of sleep deprivation suggests that there might be alterations in the ATP/AMP ratio as wakefulness is extended. That phosphorylation of AMPK is increased after 6 h of sleep deprivation supports this assertion. The increase in Nrf1 and Nrf2 (Gabp) mRNA after 6 h of sleep deprivation provides a mechanism by which there is up-regulation of key proteins.

Conclusions: There are complex dynamic changes in brain energy regulation with extended wakefulness.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cerebral Cortex / metabolism*
  • Cyclooxygenase 1 / metabolism
  • Disease Models, Animal
  • Electron Transport Complex IV / metabolism
  • Energy Metabolism*
  • Ion Channels / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mitochondrial Proteins / metabolism
  • Mitochondrial Proton-Translocating ATPases / metabolism
  • Phosphotransferases (Phosphate Group Acceptor) / metabolism
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Sleep Deprivation / metabolism*
  • Time Factors
  • Transcription Factors / metabolism
  • Uncoupling Protein 2
  • Wakefulness*

Substances

  • Ion Channels
  • Membrane Proteins
  • Mitochondrial Proteins
  • Transcription Factors
  • Ucp2 protein, mouse
  • Uncoupling Protein 2
  • Cyclooxygenase 1
  • Prostaglandin-Endoperoxide Synthases
  • Ptgs1 protein, mouse
  • Electron Transport Complex IV
  • AMP-dependent kinase (ATP-forming)
  • Phosphotransferases (Phosphate Group Acceptor)
  • ATP5b protein, mouse
  • Mitochondrial Proton-Translocating ATPases