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Effective connectivity changes in LSD-induced altered states of consciousness in humans

Psychedelics exert unique effects on human consciousness. The thalamic filter model suggests that core effects of psychedelics may result from gating deficits, based on a disintegration of information processing within cortico–striato–thalamo-cortical (CSTC) feedback loops. To test this hypothesis,...

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Autores principales: Preller, Katrin H., Razi, Adeel, Zeidman, Peter, Stämpfli, Philipp, Friston, Karl J., Vollenweider, Franz X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377471/
https://www.ncbi.nlm.nih.gov/pubmed/30692255
http://dx.doi.org/10.1073/pnas.1815129116
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author Preller, Katrin H.
Razi, Adeel
Zeidman, Peter
Stämpfli, Philipp
Friston, Karl J.
Vollenweider, Franz X.
author_facet Preller, Katrin H.
Razi, Adeel
Zeidman, Peter
Stämpfli, Philipp
Friston, Karl J.
Vollenweider, Franz X.
author_sort Preller, Katrin H.
collection PubMed
description Psychedelics exert unique effects on human consciousness. The thalamic filter model suggests that core effects of psychedelics may result from gating deficits, based on a disintegration of information processing within cortico–striato–thalamo-cortical (CSTC) feedback loops. To test this hypothesis, we characterized changes in directed (effective) connectivity between selected CTSC regions after acute administration of lysergic acid diethylamide (LSD), and after pretreatment with Ketanserin (a selective serotonin 2A receptor antagonist) plus LSD in a double-blind, randomized, placebo-controlled, cross-over study in 25 healthy participants. We used spectral dynamic causal modeling (DCM) for resting-state fMRI data. Fully connected DCM models were specified for each treatment condition to investigate the connectivity between the following areas: thalamus, ventral striatum, posterior cingulate cortex, and temporal cortex. Our results confirm major predictions proposed in the CSTC model and provide evidence that LSD alters effective connectivity within CSTC pathways that have been implicated in the gating of sensory and sensorimotor information to the cortex. In particular, LSD increased effective connectivity from the thalamus to the posterior cingulate cortex in a way that depended on serotonin 2A receptor activation, and decreased effective connectivity from the ventral striatum to the thalamus independently of serotonin 2A receptor activation. Together, these results advance our mechanistic understanding of the action of psychedelics in health and disease. This is important for the development of new pharmacological therapeutics and also increases our understanding of the mechanisms underlying the potential clinical efficacy of psychedelics.
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spelling pubmed-63774712019-02-20 Effective connectivity changes in LSD-induced altered states of consciousness in humans Preller, Katrin H. Razi, Adeel Zeidman, Peter Stämpfli, Philipp Friston, Karl J. Vollenweider, Franz X. Proc Natl Acad Sci U S A Biological Sciences Psychedelics exert unique effects on human consciousness. The thalamic filter model suggests that core effects of psychedelics may result from gating deficits, based on a disintegration of information processing within cortico–striato–thalamo-cortical (CSTC) feedback loops. To test this hypothesis, we characterized changes in directed (effective) connectivity between selected CTSC regions after acute administration of lysergic acid diethylamide (LSD), and after pretreatment with Ketanserin (a selective serotonin 2A receptor antagonist) plus LSD in a double-blind, randomized, placebo-controlled, cross-over study in 25 healthy participants. We used spectral dynamic causal modeling (DCM) for resting-state fMRI data. Fully connected DCM models were specified for each treatment condition to investigate the connectivity between the following areas: thalamus, ventral striatum, posterior cingulate cortex, and temporal cortex. Our results confirm major predictions proposed in the CSTC model and provide evidence that LSD alters effective connectivity within CSTC pathways that have been implicated in the gating of sensory and sensorimotor information to the cortex. In particular, LSD increased effective connectivity from the thalamus to the posterior cingulate cortex in a way that depended on serotonin 2A receptor activation, and decreased effective connectivity from the ventral striatum to the thalamus independently of serotonin 2A receptor activation. Together, these results advance our mechanistic understanding of the action of psychedelics in health and disease. This is important for the development of new pharmacological therapeutics and also increases our understanding of the mechanisms underlying the potential clinical efficacy of psychedelics. National Academy of Sciences 2019-02-12 2019-01-28 /pmc/articles/PMC6377471/ /pubmed/30692255 http://dx.doi.org/10.1073/pnas.1815129116 Text en Copyright © 2019 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Preller, Katrin H.
Razi, Adeel
Zeidman, Peter
Stämpfli, Philipp
Friston, Karl J.
Vollenweider, Franz X.
Effective connectivity changes in LSD-induced altered states of consciousness in humans
title Effective connectivity changes in LSD-induced altered states of consciousness in humans
title_full Effective connectivity changes in LSD-induced altered states of consciousness in humans
title_fullStr Effective connectivity changes in LSD-induced altered states of consciousness in humans
title_full_unstemmed Effective connectivity changes in LSD-induced altered states of consciousness in humans
title_short Effective connectivity changes in LSD-induced altered states of consciousness in humans
title_sort effective connectivity changes in lsd-induced altered states of consciousness in humans
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377471/
https://www.ncbi.nlm.nih.gov/pubmed/30692255
http://dx.doi.org/10.1073/pnas.1815129116
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