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Knockout serotonin transporter in rats moderates outcome and stimulus generalization
Understanding the common dimension of mental disorders (such as anxiety, depression, and drug addiction) might contribute to the construction of biological frameworks (Research Domain Criteria, RDoC) for novel ways of treatment. One common dimension at the behavioral level observed across these diso...
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/PMC7791109/ https://www.ncbi.nlm.nih.gov/pubmed/33414390 http://dx.doi.org/10.1038/s41398-020-01162-0 |
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author | Guo, Chao Ciu-Gwok He, Tao Grandjean, Joanes Homberg, Judith |
author_facet | Guo, Chao Ciu-Gwok He, Tao Grandjean, Joanes Homberg, Judith |
author_sort | Guo, Chao Ciu-Gwok |
collection | PubMed |
description | Understanding the common dimension of mental disorders (such as anxiety, depression, and drug addiction) might contribute to the construction of biological frameworks (Research Domain Criteria, RDoC) for novel ways of treatment. One common dimension at the behavioral level observed across these disorders is a generalization. Testing generalization in serotonin transporter (5-HTT) knockout (KO) rats, an animal model showing depression/anxiety-like behaviors and drug addiction-like behaviors, could therefore provide more insights into this framework. We tested the outcome and stimulus generalization in wild-type (WT) and 5-HTT KO rats. Using a newly established touchscreen-based task, subjects directly responded to visual stimuli (Gabor patch images). We measured the response time and outcome in a precise manner. We found that 5-HTT KO rats processed visual information faster than WT rats during outcome generalization. Interestingly, during stimulus generalization, WT rats gradually responded faster to the stimuli as the sessions progressed, while 5-HTT KO rats responded faster than WT in the initial sessions and did not change significantly as the sessions progressed. This observation suggests that KO rats, compared to WT rats, may be less able to update changes in information. Taken together, KO 5-HTT modulates information processing when the environment changes. |
format | Online Article Text |
id | pubmed-7791109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77911092021-01-15 Knockout serotonin transporter in rats moderates outcome and stimulus generalization Guo, Chao Ciu-Gwok He, Tao Grandjean, Joanes Homberg, Judith Transl Psychiatry Article Understanding the common dimension of mental disorders (such as anxiety, depression, and drug addiction) might contribute to the construction of biological frameworks (Research Domain Criteria, RDoC) for novel ways of treatment. One common dimension at the behavioral level observed across these disorders is a generalization. Testing generalization in serotonin transporter (5-HTT) knockout (KO) rats, an animal model showing depression/anxiety-like behaviors and drug addiction-like behaviors, could therefore provide more insights into this framework. We tested the outcome and stimulus generalization in wild-type (WT) and 5-HTT KO rats. Using a newly established touchscreen-based task, subjects directly responded to visual stimuli (Gabor patch images). We measured the response time and outcome in a precise manner. We found that 5-HTT KO rats processed visual information faster than WT rats during outcome generalization. Interestingly, during stimulus generalization, WT rats gradually responded faster to the stimuli as the sessions progressed, while 5-HTT KO rats responded faster than WT in the initial sessions and did not change significantly as the sessions progressed. This observation suggests that KO rats, compared to WT rats, may be less able to update changes in information. Taken together, KO 5-HTT modulates information processing when the environment changes. Nature Publishing Group UK 2021-01-07 /pmc/articles/PMC7791109/ /pubmed/33414390 http://dx.doi.org/10.1038/s41398-020-01162-0 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Guo, Chao Ciu-Gwok He, Tao Grandjean, Joanes Homberg, Judith Knockout serotonin transporter in rats moderates outcome and stimulus generalization |
title | Knockout serotonin transporter in rats moderates outcome and stimulus generalization |
title_full | Knockout serotonin transporter in rats moderates outcome and stimulus generalization |
title_fullStr | Knockout serotonin transporter in rats moderates outcome and stimulus generalization |
title_full_unstemmed | Knockout serotonin transporter in rats moderates outcome and stimulus generalization |
title_short | Knockout serotonin transporter in rats moderates outcome and stimulus generalization |
title_sort | knockout serotonin transporter in rats moderates outcome and stimulus generalization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791109/ https://www.ncbi.nlm.nih.gov/pubmed/33414390 http://dx.doi.org/10.1038/s41398-020-01162-0 |
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