Enhanced repertoire of brain dynamical states during the psychedelic experience (1405.6466v1)

Abstract: The study of rapid changes in brain dynamics and functional connectivity (FC) is of increasing interest in neuroimaging. Brain states departing from normal waking consciousness are expected to be accompanied by alterations in the aforementioned dynamics. In particular, the psychedelic experience produced by psilocybin (a substance found in magic mushrooms) is characterized by unconstrained cognition and profound alterations in the perception of time, space and selfhood. Considering the spontaneous and subjective manifestation of these effects, we hypothesize that neural correlates of the psychedelic experience can be found in the dynamics and variability of spontaneous brain activity fluctuations and connectivity, measurable with functional Magnetic Resonance Imaging (fMRI). Fifteen healthy subjects were scanned before, during and after intravenous infusion of psilocybin and an inert placebo. Blood-Oxygen Level Dependent (BOLD) temporal variability was assessed computing the variance and total spectral power, resulting in increased signal variability bilaterally in the hippocampi and anterior cingulate cortex. Changes in BOLD signal spectral behavior (including spectral scaling exponents) affected exclusively higher brain systems such as the default mode, executive control and dorsal attention networks. A novel framework enabled us to track different connectivity states explored by the brain during rest. This approach revealed a wider repertoire of connectivity states post-psilocybin than during control conditions. Together, the present results provide a comprehensive account of the effects of psilocybin on dynamical behaviour in the human brain at a macroscopic level and may have implications for our understanding of the unconstrained, hyper-associative quality of consciousness in the psychedelic state.

• The paper demonstrates that psilocybin markedly increases BOLD signal variability in key regions like the hippocampi and anterior cingulate cortex.
• The paper applies a placebo-controlled fMRI methodology to reveal altered spectral dynamics, including reduced low-frequency power.
• The paper uncovers an expanded repertoire of connectivity states, quantified by higher Shannon entropy, linking neurophysiology to altered consciousness.

Enhanced Repertoire of Brain Dynamical States During the Psychedelic Experience

The paper "Enhanced Repertoire of Brain Dynamical States During the Psychedelic Experience" investigates the alterations in brain dynamics and functional connectivity resulting from the administration of psilocybin, a compound found in psychedelic mushrooms. Utilizing functional Magnetic Resonance Imaging (fMRI) to paper the resting state brain activity of 15 healthy participants, the research assesses the impact of psilocybin on the variability and dynamical states of the brain's macroscopic networks.

The paper is grounded in the hypothesis that the psychedelic state, characterized by hyper-associative cognition and altered perception, can be correlated with distinct changes in brain dynamics and spontaneous activity fluctuations. Specifically, the authors focus on evaluating the temporal variability in the Blood-Oxygen Level Dependent (BOLD) signal and how this reflects altered functional connectivity and brain state dynamics post-psilocybin infusion.

Methodology and Analysis

A placebo-controlled experiment was conducted wherein participants underwent fMRI scans before, during, and after the infusion of either psilocybin or a saline placebo. The paper primarily analyzes the BOLD signal's variance and total spectral power, observing significant increases in the hippocampi and anterior cingulate cortex after psilocybin administration. The results indicate enhanced temporal variability in these regions, suggesting increased signal fluctuations.

In a novel approach, the researchers employ a framework to analyze brain connectivity states, revealing a broader array of connectivity states post-psilocybin infusion compared to the placebo condition. This is quantified through Shannon entropy, indicating a higher diversity of dynamical states when the brain is under the influence of psilocybin.

Key Findings

1. Increased BOLD Variability: The psilocybin condition exhibited heightened BOLD variance and spectral power, with significant signal variability noted bilaterally in the hippocampi and anterior cingulate cortex. This suggests enhanced signal fluctuations and potential synaptic synchronization in these regions.
2. Altered Spectral Dynamics: A reduction in low-frequency power and frequency scaling exponent was observed in higher brain regions, aligning with decreased neuronal coherence and enhanced entropy.
3. Enhanced Dynamical Connectivity: The extensive repertoire of connectivity states under psilocybin reflects a potential neural substrate for the expanded consciousness reported during psychedelic experiences. This is exemplified by an increase in connectivity motifs and entropy in the hippocampal/ACC network.

Implications and Future Directions

The implications of this research extend to both theoretical and practical domains. The observed increase in brain dynamics and connectivity states provides insight into the potential neural basis for the subjective experiences associated with psychedelics. Understanding how psilocybin modulates brain activity could inform novel therapeutic approaches for psychiatric disorders, drawing parallels with conditions like psychosis and REM sleep states.

Future research could leverage this paper's methodologies to explore the broader spectrum of dynamical states in altered consciousness and assess the therapeutic potential of psychedelics in neuropsychiatric contexts. Additionally, further investigation into the specific interaction of psychedelics with neuronal networks could elucidate more precise mechanisms underlying consciousness expansion.

This paper marks a significant stride in comprehending the neurophysiological impact of psychedelics on human consciousness by linking macroscopic brain changes to altered subjective experiences.