Changes in the composition of brain interstitial ions control the sleep-wake cycle

Science. 2016 Apr 29;352(6285):550-5. doi: 10.1126/science.aad4821.

Abstract

Wakefulness is driven by the widespread release of neuromodulators by the ascending arousal system. Yet, it is unclear how these substances orchestrate state-dependent, global changes in neuronal activity. Here, we show that neuromodulators induce increases in the extracellular K(+) concentration ([K(+)]e) in cortical slices electrically silenced by tetrodotoxin. In vivo, arousal was linked to AMPA receptor-independent elevations of [K(+)]e concomitant with decreases in [Ca(2+)]e, [Mg(2+)]e, [H(+)]e, and the extracellular volume. Opposite, natural sleep and anesthesia reduced [K(+)]e while increasing [Ca(2+)]e, [Mg(2+)]e, and [H(+)]e as well as the extracellular volume. Local cortical activity of sleeping mice could be readily converted to the stereotypical electroencephalography pattern of wakefulness by simply imposing a change in the extracellular ion composition. Thus, extracellular ions control the state-dependent patterns of neural activity.

Publication types

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

MeSH terms

  • Animals
  • Calcium / analysis
  • Calcium / metabolism
  • Cations / analysis
  • Cations / metabolism*
  • Cerebral Cortex / chemistry
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / physiology*
  • Electroencephalography
  • Magnesium / analysis
  • Magnesium / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / physiology
  • Neurotransmitter Agents / metabolism
  • Neurotransmitter Agents / pharmacology
  • Potassium / metabolism*
  • Receptors, AMPA / metabolism
  • Sleep / drug effects
  • Sleep / physiology*
  • Sodium Channel Blockers / pharmacology
  • Tetrodotoxin / pharmacology
  • Wakefulness / drug effects
  • Wakefulness / physiology*

Substances

  • Cations
  • Neurotransmitter Agents
  • Receptors, AMPA
  • Sodium Channel Blockers
  • Tetrodotoxin
  • Magnesium
  • Potassium
  • Calcium