Bidirectional communication between the cortex and thalamus via a specific cross-frequency channel is linked to conscious states. In humans, mice, and rats, low-frequency waves (1–13 Hz) sent from either the cortex or thalamus are consistently encoded by the other region using high gamma waves (52–104 Hz). This cross-frequency communication is diminished during propofol-induced unconsciousness and generalized spike-and-wave seizures, but enhanced by the psychedelic 5-MeO-DMT. Numerical simulations and neural recordings suggest these changes are mediated by shifts in thalamocortical electrodynamics toward or away from edge-of-chaos criticality, offering a mathematical framework for disrupted information transfer during unconsciousness.
Consciousness depends on bidirectional communication between the cortex and thalamus. A specific pattern of cross-frequency communication—low-frequency waves (1.5–13 Hz) from one region encoded as high gamma waves (50–100 Hz) in the other—is present during conscious states in humans, mice, and rats. This communication diminishes during propofol-induced anesthesia and generalized spike-and-wave seizures, but is enhanced by the psychedelic 5-MeO-DMT. Numerical simulations and neural recordings show that these changes are mediated by shifts in thalamocortical dynamics toward or away from edge-of-chaos criticality, the phase transition between stability and chaos. The findings offer a mathematically defined framework linking thalamic-cortical communication to consciousness.