Cortical hypersynchrony predicts breakdown of sensory processing during loss of consciousness

Curr Biol. 2011 Dec 6;21(23):1988-93. doi: 10.1016/j.cub.2011.10.017. Epub 2011 Nov 17.

Abstract

Intrinsic cortical dynamics modulates the processing of sensory information and therefore may be critical for conscious perception. We tested this hypothesis by electroencephalographic recording of ongoing and stimulus-related brain activity during stepwise drug-induced loss of consciousness in healthy human volunteers. We found that progressive loss of consciousness was tightly linked to the emergence of a hypersynchronous cortical state in the alpha frequency range (8-14 Hz). This drug-induced ongoing alpha activity was widely distributed across the frontal cortex. Stimulus-related responses to median nerve stimulation consisted of early and midlatency response components in primary somatosensory cortex (S1) and a late component also involving temporal and parietal regions. During progressive sedation, the early response was maintained, whereas the midlatency and late responses were reduced and eventually vanished. The antagonistic relation between the late sensory response and ongoing alpha activity held for constant drug levels on the single-trial level. Specifically, the late response component was negatively correlated with the power and long-range coherence of ongoing frontal alpha activity. Our results suggest blocking of intracortical communication by hypersynchronous ongoing activity as a key mechanism for the loss of consciousness.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alpha Rhythm / drug effects
  • Alpha Rhythm / physiology*
  • Brain Mapping
  • Cerebral Cortex / physiology*
  • Electroencephalography
  • Electroencephalography Phase Synchronization / drug effects
  • Electroencephalography Phase Synchronization / physiology*
  • Humans
  • Male
  • Perception / physiology*
  • Propofol / pharmacology
  • Unconsciousness / chemically induced
  • Unconsciousness / physiopathology*

Substances

  • Propofol