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Psilocybin induces dose-dependent changes in functional network organization in rat cortex

Brian H Silverstein, Nicholas Kolbman, Amanda Nelson, Tiecheng Liu, Peter Guzzo, Jim Gilligan, UnCheol Lee, George A Mashour, Giancarlo Vanini, Dinesh Pal

bioRxiv (Cold Spring Harbor Laboratory) February 12, 2024 preprint DOI: 10.1101/2024.02.09.579718 via OpenAlex

Summary

AI-generated from the abstract

Psilocybin disrupts the coupling between theta and gamma brain waves in rats and reorganizes brain networks in a dose-dependent manner. Using 27 electrodes across the cortex, the study found that psilocybin increased frontal high gamma connectivity and posterior theta connectivity, as well as network density in those regions. Medium gamma frontoparietal connectivity showed a nonlinear relationship with dose. Theta-gamma phase-amplitude coupling was disrupted. These changes suggest that high-frequency network organization, decoupled from local theta-phase, may be a signature of the altered state of consciousness induced by psilocybin.

Study at a glance

Characteristics Observational study
Sample size 12
Population Male and female rats
Intervention Psilocybin
Dose 0.1 mg/kg, 1 mg/kg, and 10 mg/kg delivered over an hour
Topics Psilocybin
Keywords High gamma oscillations Phase-amplitude coupling Rat Weighted phase-lag index Neuroscience
Citations 3
Key finding Psilocybin dose-dependently disrupted theta-gamma coupling, increased frontal high gamma and posterior theta connectivity and network density, and produced nonlinear changes in medium gamma frontoparietal connectivity.

Abstract

Abstract Psilocybin produces an altered state of consciousness in humans and is associated with complex spatiotemporal changes in brain networks. Given the emphasis on rodent models for mechanistic studies, there is a need for characterization of the effect of psilocybin on brain-wide network dynamics. Previous rodent studies of psychedelics, using electroencephalogram, have primarily been done with sparse electrode arrays that offered limited spatial resolution precluding network level analysis, and have been restricted to lower gamma frequencies. Therefore, in the study, we used electroencephalographic recordings from 27 sites (electrodes) across rat cortex ( n =6 male, 6 female) to characterize the effect of psilocybin (0.1 mg/kg, 1 mg/kg, and 10 mg/kg delivered over an hour) on network organization as inferred through changes in node degree (index of network density) and connection strength (weighted phase-lag index). The removal of aperiodic component from the electroencephalogram localized the primary oscillatory changes to theta (4-10 Hz), medium gamma (70-110 Hz), and high gamma (110-150 Hz) bands, which were used for the network analysis. Additionally, we determined the concurrent changes in theta-gamma phase-amplitude coupling. We report that psilocybin, in a dose-dependent manner, 1) disrupted theta-gamma coupling [ p <0.05], 2) increased frontal high gamma connectivity [ p <0.05] and posterior theta connectivity [ p ≤0.049], and 3) increased frontal high gamma [ p <0.05] and posterior theta [ p ≤0.046] network density. The medium gamma frontoparietal connectivity showed a nonlinear relationship with psilocybin dose. Our results suggest that high-frequency network organization, decoupled from local theta-phase, may be an important signature of psilocybin-induced non-ordinary state of consciousness.

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