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Thigmotaxis in a virtual human open field test
Animal models are used to study neurobiological mechanisms in mental disorders. Although there has been significant progress in the understanding of neurobiological underpinnings of threat-related behaviors and anxiety, little progress was made with regard to new or improved treatments for mental di...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988123/ https://www.ncbi.nlm.nih.gov/pubmed/33758204 http://dx.doi.org/10.1038/s41598-021-85678-5 |
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author | Gromer, Daniel Kiser, Dominik P. Pauli, Paul |
author_facet | Gromer, Daniel Kiser, Dominik P. Pauli, Paul |
author_sort | Gromer, Daniel |
collection | PubMed |
description | Animal models are used to study neurobiological mechanisms in mental disorders. Although there has been significant progress in the understanding of neurobiological underpinnings of threat-related behaviors and anxiety, little progress was made with regard to new or improved treatments for mental disorders. A possible reason for this lack of success is the unknown predictive and cross-species translational validity of animal models used in preclinical studies. Re-translational approaches, therefore, seek to establish cross-species translational validity by identifying behavioral operations shared across species. To this end, we implemented a human open field test in virtual reality and measured behavioral indices derived from animal studies in three experiments ([Formula: see text] , [Formula: see text] , and [Formula: see text] ). In addition, we investigated the associations between anxious traits and such behaviors. Results indicated a strong similarity in behavior across species, i.e., participants in our study—like rodents in animal studies—preferred to stay in the outer region of the open field, as indexed by multiple behavioral parameters. However, correlational analyses did not clearly indicate that these behaviors were a function of anxious traits of participants. We conclude that the realized virtual open field test is able to elicit thigmotaxis and thus demonstrates cross-species validity of this aspect of the test. Modulatory effects of anxiety on human open field behavior should be examined further by incorporating possible threats in the virtual scenario and/or by examining participants with higher anxiety levels or anxiety disorder patients. |
format | Online Article Text |
id | pubmed-7988123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79881232021-03-25 Thigmotaxis in a virtual human open field test Gromer, Daniel Kiser, Dominik P. Pauli, Paul Sci Rep Article Animal models are used to study neurobiological mechanisms in mental disorders. Although there has been significant progress in the understanding of neurobiological underpinnings of threat-related behaviors and anxiety, little progress was made with regard to new or improved treatments for mental disorders. A possible reason for this lack of success is the unknown predictive and cross-species translational validity of animal models used in preclinical studies. Re-translational approaches, therefore, seek to establish cross-species translational validity by identifying behavioral operations shared across species. To this end, we implemented a human open field test in virtual reality and measured behavioral indices derived from animal studies in three experiments ([Formula: see text] , [Formula: see text] , and [Formula: see text] ). In addition, we investigated the associations between anxious traits and such behaviors. Results indicated a strong similarity in behavior across species, i.e., participants in our study—like rodents in animal studies—preferred to stay in the outer region of the open field, as indexed by multiple behavioral parameters. However, correlational analyses did not clearly indicate that these behaviors were a function of anxious traits of participants. We conclude that the realized virtual open field test is able to elicit thigmotaxis and thus demonstrates cross-species validity of this aspect of the test. Modulatory effects of anxiety on human open field behavior should be examined further by incorporating possible threats in the virtual scenario and/or by examining participants with higher anxiety levels or anxiety disorder patients. Nature Publishing Group UK 2021-03-23 /pmc/articles/PMC7988123/ /pubmed/33758204 http://dx.doi.org/10.1038/s41598-021-85678-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gromer, Daniel Kiser, Dominik P. Pauli, Paul Thigmotaxis in a virtual human open field test |
title | Thigmotaxis in a virtual human open field test |
title_full | Thigmotaxis in a virtual human open field test |
title_fullStr | Thigmotaxis in a virtual human open field test |
title_full_unstemmed | Thigmotaxis in a virtual human open field test |
title_short | Thigmotaxis in a virtual human open field test |
title_sort | thigmotaxis in a virtual human open field test |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988123/ https://www.ncbi.nlm.nih.gov/pubmed/33758204 http://dx.doi.org/10.1038/s41598-021-85678-5 |
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