Ibogaine, a psychedelic alkaloid with anti-addictive potential, produces vivid, dream-like experiences while awake. Analyzing intracranial electroencephalograms in rats, ibogaine-induced wakefulness showed gamma oscillations with greater power than control levels but reduced coherence and complexity. This gamma activity profile resembled that of natural REM sleep, providing biological evidence linking the psychedelic state to REM sleep and advancing understanding of ibogaine's oneirogenic effects.
The psychedelic 5-MeO-DMT alters brain activity in rats by increasing delta waves and decreasing theta waves in the hippocampus, changes that are not explained by movement. It also reduces slow and mid gamma power and disrupts theta phase modulation. The overall brain state resembles patterns seen during slow-wave sleep and REM sleep, suggesting that the drug's effects involve mixing waking behavior with sleep-like neural oscillations.
Slow oscillations in the brain’s parietal cortex during urethane anesthesia differ fundamentally from those during natural non-REM sleep in mice, despite appearing similar on the surface. Differences are evident in the local field potential, the underlying current sources, and the modulation of unit activity. The data show that slow network oscillations in natural sleep and anesthesia are generated by different mechanisms, challenging the assumption that anesthesia reliably models sleep-related brain activity. This work highlights that phenomenological similarities can mask distinct neural processes, with implications for using anesthesia as a model for sleep and consciousness studies.