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MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor

Previous research has shown that a single dose of MDMA induce a dissociative state, by elevating feelings of depersonalization and derealization. Typically, it is assumed that action on the 5-HT(2A) receptor is the mechanism underlying these psychedelic experiences. In addition, other studies have s...

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Autores principales: Puxty, Drew J., Ramaekers, Johannes G., de la Torre, Rafael, Farré, Magí, Pizarro, Neus, Pujadas, Mitona, Kuypers, Kim P. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504523/
https://www.ncbi.nlm.nih.gov/pubmed/28744219
http://dx.doi.org/10.3389/fphar.2017.00455
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author Puxty, Drew J.
Ramaekers, Johannes G.
de la Torre, Rafael
Farré, Magí
Pizarro, Neus
Pujadas, Mitona
Kuypers, Kim P. C.
author_facet Puxty, Drew J.
Ramaekers, Johannes G.
de la Torre, Rafael
Farré, Magí
Pizarro, Neus
Pujadas, Mitona
Kuypers, Kim P. C.
author_sort Puxty, Drew J.
collection PubMed
description Previous research has shown that a single dose of MDMA induce a dissociative state, by elevating feelings of depersonalization and derealization. Typically, it is assumed that action on the 5-HT(2A) receptor is the mechanism underlying these psychedelic experiences. In addition, other studies have shown associations between dissociative states and biological parameters (heart rate, cortisol), which are elevated by MDMA. In order to investigate the role of the 5-HT(2) receptor in the MDMA-induced dissociative state and the association with biological parameters, a placebo-controlled within-subject study was conducted including a single oral dose of MDMA (75 mg), combined with placebo or a single oral dose of the 5-HT(2) receptor blocker ketanserin (40 mg). Twenty healthy recreational MDMA users filled out a dissociative states scale (CADSS) 90 min after treatments, which was preceded and followed by assessment of a number of biological parameters (cortisol levels, heart rate, MDMA blood concentrations). Findings showed that MDMA induced a dissociative state but this effect was not counteracted by pre-treatment with ketanserin. Heart rate was the only biological parameter that correlated with the MDMA-induced dissociative state, but an absence of correlation between these measures when participants were pretreated with ketanserin suggests an absence of directional effects of heart rate on dissociative state. It is suggested that the 5-HT(2) receptor does not mediate the dissociative effects caused by a single dose of MDMA. Further research is needed to determine the exact neurobiology underlying this effect and whether these effects contribute to the therapeutic potential of MDMA.
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spelling pubmed-55045232017-07-25 MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor Puxty, Drew J. Ramaekers, Johannes G. de la Torre, Rafael Farré, Magí Pizarro, Neus Pujadas, Mitona Kuypers, Kim P. C. Front Pharmacol Pharmacology Previous research has shown that a single dose of MDMA induce a dissociative state, by elevating feelings of depersonalization and derealization. Typically, it is assumed that action on the 5-HT(2A) receptor is the mechanism underlying these psychedelic experiences. In addition, other studies have shown associations between dissociative states and biological parameters (heart rate, cortisol), which are elevated by MDMA. In order to investigate the role of the 5-HT(2) receptor in the MDMA-induced dissociative state and the association with biological parameters, a placebo-controlled within-subject study was conducted including a single oral dose of MDMA (75 mg), combined with placebo or a single oral dose of the 5-HT(2) receptor blocker ketanserin (40 mg). Twenty healthy recreational MDMA users filled out a dissociative states scale (CADSS) 90 min after treatments, which was preceded and followed by assessment of a number of biological parameters (cortisol levels, heart rate, MDMA blood concentrations). Findings showed that MDMA induced a dissociative state but this effect was not counteracted by pre-treatment with ketanserin. Heart rate was the only biological parameter that correlated with the MDMA-induced dissociative state, but an absence of correlation between these measures when participants were pretreated with ketanserin suggests an absence of directional effects of heart rate on dissociative state. It is suggested that the 5-HT(2) receptor does not mediate the dissociative effects caused by a single dose of MDMA. Further research is needed to determine the exact neurobiology underlying this effect and whether these effects contribute to the therapeutic potential of MDMA. Frontiers Media S.A. 2017-07-11 /pmc/articles/PMC5504523/ /pubmed/28744219 http://dx.doi.org/10.3389/fphar.2017.00455 Text en Copyright © 2017 Puxty, Ramaekers, de la Torre, Farré, Pizarro, Pujadas and Kuypers. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Puxty, Drew J.
Ramaekers, Johannes G.
de la Torre, Rafael
Farré, Magí
Pizarro, Neus
Pujadas, Mitona
Kuypers, Kim P. C.
MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor
title MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor
title_full MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor
title_fullStr MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor
title_full_unstemmed MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor
title_short MDMA-Induced Dissociative State not Mediated by the 5-HT(2A) Receptor
title_sort mdma-induced dissociative state not mediated by the 5-ht(2a) receptor
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504523/
https://www.ncbi.nlm.nih.gov/pubmed/28744219
http://dx.doi.org/10.3389/fphar.2017.00455
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