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LSD induces increased signalling entropy in rats’ prefrontal cortex

Aurora Savino, Charles D. Nichols

bioRxiv (Cold Spring Harbor Laboratory) June 23, 2021 preprint DOI: 10.1101/2021.06.23.449556 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational study
Population Prefrontal cortex of rats
Intervention Lysergic acid diethylamide (LSD)
Duration Chronic treatment
Topics LSD Neuroplasticity Serotonin
Keywords Prefrontal cortex Signalling Neuroimaging Receptor Cognition Cell biology Biochemistry
Citations 2
Key findings Chronic LSD treatment rewires gene co-expression networks in the rat prefrontal cortex, making them less centralized but more complex with increased signaling entropy.

Abstract

Abstract Psychedelic drugs are gaining attention from the scientific community as potential new compounds for the treatment of psychiatric diseases such as mood and substance use disorders. The 5-HT 2A receptor has been identified as the main molecular target, and early studies pointed to an effect on the expression of neuroplasticity genes. Analysing RNA-seq data from the prefrontal cortex of rats chronically treated with lysergic acid diethylamide (LSD), we describe the psychedelic-induced rewiring of gene co-expression networks, which become less centralized but more complex, with an overall increase in signalling entropy, typical of highly plastic systems. Intriguingly, signalling entropy mirrors, at the molecular level, the increased brain entropy reported through neuroimaging studies in human, suggesting the underlying mechanisms of higher-order phenomena. Moreover, from the analysis of network topology we identify potential transcriptional regulators and imply different cell types in psychedelics’ activity.

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