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A unified model of ketamine’s dissociative and psychedelic properties

Ketamine is an N-methyl-d-aspartate antagonist which is increasingly being researched and used as a treatment for depression. In low doses, it can cause a transitory modification in consciousness which was classically labelled as ‘dissociation’. However, ketamine is also commonly classified as an at...

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Autores principales: Marguilho, Miriam, Figueiredo, Inês, Castro-Rodrigues, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834329/
https://www.ncbi.nlm.nih.gov/pubmed/36527355
http://dx.doi.org/10.1177/02698811221140011
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author Marguilho, Miriam
Figueiredo, Inês
Castro-Rodrigues, Pedro
author_facet Marguilho, Miriam
Figueiredo, Inês
Castro-Rodrigues, Pedro
author_sort Marguilho, Miriam
collection PubMed
description Ketamine is an N-methyl-d-aspartate antagonist which is increasingly being researched and used as a treatment for depression. In low doses, it can cause a transitory modification in consciousness which was classically labelled as ‘dissociation’. However, ketamine is also commonly classified as an atypical psychedelic and it has been recently reported that ego dissolution experiences during ketamine administration are associated with greater antidepressant response. Neuroimaging studies have highlighted several similarities between the effects of ketamine and those of serotonergic psychedelics in the brain; however, no unified account has been proposed for ketamine’s multi-level effects – from molecular to network and psychological levels. Here, we propose that the fast, albeit transient, antidepressant effects observed after ketamine infusions are mainly driven by its acute modulation of reward circuits and sub-acute increase in neuroplasticity, while its dissociative and psychedelic properties are driven by dose- and context-dependent disruption of large-scale functional networks. Computationally, as nodes of the salience network (SN) represent high-level priors about the body (‘minimal’ self) and nodes of the default-mode network (DMN) represent the highest-level priors about narrative self-experience (‘biographical’ self), we propose that transitory SN desegregation and disintegration accounts for ketamine’s ‘dissociative’ state, while transitory DMN desegregation and disintegration accounts for ketamine’s ‘psychedelic’ state. In psychedelic-assisted psychotherapy, a relaxation of the highest-level beliefs with psychotherapeutic support may allow a revision of pathological self-representation models, for which neuroplasticity plays a permissive role. Our account provides a multi-level rationale for using the psychedelic properties of ketamine to increase its long-term benefits.
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spelling pubmed-98343292023-01-13 A unified model of ketamine’s dissociative and psychedelic properties Marguilho, Miriam Figueiredo, Inês Castro-Rodrigues, Pedro J Psychopharmacol Reviews Ketamine is an N-methyl-d-aspartate antagonist which is increasingly being researched and used as a treatment for depression. In low doses, it can cause a transitory modification in consciousness which was classically labelled as ‘dissociation’. However, ketamine is also commonly classified as an atypical psychedelic and it has been recently reported that ego dissolution experiences during ketamine administration are associated with greater antidepressant response. Neuroimaging studies have highlighted several similarities between the effects of ketamine and those of serotonergic psychedelics in the brain; however, no unified account has been proposed for ketamine’s multi-level effects – from molecular to network and psychological levels. Here, we propose that the fast, albeit transient, antidepressant effects observed after ketamine infusions are mainly driven by its acute modulation of reward circuits and sub-acute increase in neuroplasticity, while its dissociative and psychedelic properties are driven by dose- and context-dependent disruption of large-scale functional networks. Computationally, as nodes of the salience network (SN) represent high-level priors about the body (‘minimal’ self) and nodes of the default-mode network (DMN) represent the highest-level priors about narrative self-experience (‘biographical’ self), we propose that transitory SN desegregation and disintegration accounts for ketamine’s ‘dissociative’ state, while transitory DMN desegregation and disintegration accounts for ketamine’s ‘psychedelic’ state. In psychedelic-assisted psychotherapy, a relaxation of the highest-level beliefs with psychotherapeutic support may allow a revision of pathological self-representation models, for which neuroplasticity plays a permissive role. Our account provides a multi-level rationale for using the psychedelic properties of ketamine to increase its long-term benefits. SAGE Publications 2022-12-17 2023-01 /pmc/articles/PMC9834329/ /pubmed/36527355 http://dx.doi.org/10.1177/02698811221140011 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Reviews
Marguilho, Miriam
Figueiredo, Inês
Castro-Rodrigues, Pedro
A unified model of ketamine’s dissociative and psychedelic properties
title A unified model of ketamine’s dissociative and psychedelic properties
title_full A unified model of ketamine’s dissociative and psychedelic properties
title_fullStr A unified model of ketamine’s dissociative and psychedelic properties
title_full_unstemmed A unified model of ketamine’s dissociative and psychedelic properties
title_short A unified model of ketamine’s dissociative and psychedelic properties
title_sort unified model of ketamine’s dissociative and psychedelic properties
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834329/
https://www.ncbi.nlm.nih.gov/pubmed/36527355
http://dx.doi.org/10.1177/02698811221140011
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