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An elevated plus-maze in mixed reality for studying human anxiety-related behavior

BACKGROUND: A dearth of laboratory tests to study actual human approach-avoidance behavior has complicated translational research on anxiety. The elevated plus-maze (EPM) is the gold standard to assess approach-avoidance behavior in rodents. METHODS: Here, we translated the EPM to humans using mixed...

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Autores principales: Biedermann, Sarah V., Biedermann, Daniel G., Wenzlaff, Frederike, Kurjak, Tim, Nouri, Sawis, Auer, Matthias K., Wiedemann, Klaus, Briken, Peer, Haaker, Jan, Lonsdorf, Tina B., Fuss, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740602/
https://www.ncbi.nlm.nih.gov/pubmed/29268740
http://dx.doi.org/10.1186/s12915-017-0463-6
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author Biedermann, Sarah V.
Biedermann, Daniel G.
Wenzlaff, Frederike
Kurjak, Tim
Nouri, Sawis
Auer, Matthias K.
Wiedemann, Klaus
Briken, Peer
Haaker, Jan
Lonsdorf, Tina B.
Fuss, Johannes
author_facet Biedermann, Sarah V.
Biedermann, Daniel G.
Wenzlaff, Frederike
Kurjak, Tim
Nouri, Sawis
Auer, Matthias K.
Wiedemann, Klaus
Briken, Peer
Haaker, Jan
Lonsdorf, Tina B.
Fuss, Johannes
author_sort Biedermann, Sarah V.
collection PubMed
description BACKGROUND: A dearth of laboratory tests to study actual human approach-avoidance behavior has complicated translational research on anxiety. The elevated plus-maze (EPM) is the gold standard to assess approach-avoidance behavior in rodents. METHODS: Here, we translated the EPM to humans using mixed reality through a combination of virtual and real-world elements. In two validation studies, we observed participants’ anxiety on a behavioral, physiological, and subjective level. RESULTS: Participants reported higher anxiety on open arms, avoided open arms, and showed an activation of endogenous stress systems. Participants’ with high anxiety exhibited higher avoidance. Moreover, open arm avoidance was moderately predicted by participants’ acrophobia and sensation seeking, with opposing influences. In a randomized, double blind, placebo controlled experiment, GABAergic stimulation decreased avoidance of open arms while alpha-2-adrenergic antagonism increased avoidance. CONCLUSION: These findings demonstrate cross-species validity of open arm avoidance as a translational measure of anxiety. We thus introduce the first ecologically valid assay to track actual human approach-avoidance behavior under laboratory conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0463-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-57406022018-01-02 An elevated plus-maze in mixed reality for studying human anxiety-related behavior Biedermann, Sarah V. Biedermann, Daniel G. Wenzlaff, Frederike Kurjak, Tim Nouri, Sawis Auer, Matthias K. Wiedemann, Klaus Briken, Peer Haaker, Jan Lonsdorf, Tina B. Fuss, Johannes BMC Biol Methodology Article BACKGROUND: A dearth of laboratory tests to study actual human approach-avoidance behavior has complicated translational research on anxiety. The elevated plus-maze (EPM) is the gold standard to assess approach-avoidance behavior in rodents. METHODS: Here, we translated the EPM to humans using mixed reality through a combination of virtual and real-world elements. In two validation studies, we observed participants’ anxiety on a behavioral, physiological, and subjective level. RESULTS: Participants reported higher anxiety on open arms, avoided open arms, and showed an activation of endogenous stress systems. Participants’ with high anxiety exhibited higher avoidance. Moreover, open arm avoidance was moderately predicted by participants’ acrophobia and sensation seeking, with opposing influences. In a randomized, double blind, placebo controlled experiment, GABAergic stimulation decreased avoidance of open arms while alpha-2-adrenergic antagonism increased avoidance. CONCLUSION: These findings demonstrate cross-species validity of open arm avoidance as a translational measure of anxiety. We thus introduce the first ecologically valid assay to track actual human approach-avoidance behavior under laboratory conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0463-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-21 /pmc/articles/PMC5740602/ /pubmed/29268740 http://dx.doi.org/10.1186/s12915-017-0463-6 Text en © Fuss et al. 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Biedermann, Sarah V.
Biedermann, Daniel G.
Wenzlaff, Frederike
Kurjak, Tim
Nouri, Sawis
Auer, Matthias K.
Wiedemann, Klaus
Briken, Peer
Haaker, Jan
Lonsdorf, Tina B.
Fuss, Johannes
An elevated plus-maze in mixed reality for studying human anxiety-related behavior
title An elevated plus-maze in mixed reality for studying human anxiety-related behavior
title_full An elevated plus-maze in mixed reality for studying human anxiety-related behavior
title_fullStr An elevated plus-maze in mixed reality for studying human anxiety-related behavior
title_full_unstemmed An elevated plus-maze in mixed reality for studying human anxiety-related behavior
title_short An elevated plus-maze in mixed reality for studying human anxiety-related behavior
title_sort elevated plus-maze in mixed reality for studying human anxiety-related behavior
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740602/
https://www.ncbi.nlm.nih.gov/pubmed/29268740
http://dx.doi.org/10.1186/s12915-017-0463-6
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