Cargando…
Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter
A range of dopamine-dominating neuropsychiatric disorders present with cognitive deficits. In accordance, the dopamine transporter overexpressing rat model (DAT-tg rat) displays cognitive deficits by means of behavioral inflexibility and learning disabilities. It remains to be investigated when cogn...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616742/ https://www.ncbi.nlm.nih.gov/pubmed/36125729 http://dx.doi.org/10.1007/s12035-022-03029-5 |
_version_ | 1784820704091308032 |
---|---|
author | Edemann-Callesen, Henriette Glienke, Maximilian Akinola, Esther Olubukola Lieser, Maike Kristin Habelt, Bettina Hadar, Ravit Bernhardt, Nadine Winter, Christine |
author_facet | Edemann-Callesen, Henriette Glienke, Maximilian Akinola, Esther Olubukola Lieser, Maike Kristin Habelt, Bettina Hadar, Ravit Bernhardt, Nadine Winter, Christine |
author_sort | Edemann-Callesen, Henriette |
collection | PubMed |
description | A range of dopamine-dominating neuropsychiatric disorders present with cognitive deficits. In accordance, the dopamine transporter overexpressing rat model (DAT-tg rat) displays cognitive deficits by means of behavioral inflexibility and learning disabilities. It remains to be investigated when cognitive deficits emerge, due to the inherent DA irregularities, during the life course of the DAT-tg rat and what may relieve symptoms. The Morris water maze (MWM) was used to assess cognitive abilities in three cohorts of DAT-tg rats. In the first cohort, the development of cognitive deficits was assessed by repeatedly testing animals in the MWM at postnatal day (PND) 35, 60, and 90. In the second and third cohort, pharmacological interventions and transcranial direct current stimulation (tDCS) were tested in adult animals to understand what drives, and thus relieves, the deficits. Minor differences were observed between DAT-tg rats and control rats at PND 35 and 60, whereas cognitive deficits fully emerged at PND 90. A high dosage of methylphenidate diminished both behavioral inflexibility and improved learning abilities in adult rats. Interestingly, rats subjected early in life to the MWM also displayed improved behavioral flexibility as compared to rats naïve to the paradigm. Cognitive deficits gradually develop over time and fully emerge in adulthood. Pharmacological modulation of the ubiquitous DAT overexpression overall improves deficits in adult rats, whereas early training decreases later development of behavioral inflexibility. Thus, former training may constitute a preventive avenue that alters some aspects of cognitive deficits resulting from inherent DA abnormalities. |
format | Online Article Text |
id | pubmed-9616742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-96167422022-10-30 Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter Edemann-Callesen, Henriette Glienke, Maximilian Akinola, Esther Olubukola Lieser, Maike Kristin Habelt, Bettina Hadar, Ravit Bernhardt, Nadine Winter, Christine Mol Neurobiol Article A range of dopamine-dominating neuropsychiatric disorders present with cognitive deficits. In accordance, the dopamine transporter overexpressing rat model (DAT-tg rat) displays cognitive deficits by means of behavioral inflexibility and learning disabilities. It remains to be investigated when cognitive deficits emerge, due to the inherent DA irregularities, during the life course of the DAT-tg rat and what may relieve symptoms. The Morris water maze (MWM) was used to assess cognitive abilities in three cohorts of DAT-tg rats. In the first cohort, the development of cognitive deficits was assessed by repeatedly testing animals in the MWM at postnatal day (PND) 35, 60, and 90. In the second and third cohort, pharmacological interventions and transcranial direct current stimulation (tDCS) were tested in adult animals to understand what drives, and thus relieves, the deficits. Minor differences were observed between DAT-tg rats and control rats at PND 35 and 60, whereas cognitive deficits fully emerged at PND 90. A high dosage of methylphenidate diminished both behavioral inflexibility and improved learning abilities in adult rats. Interestingly, rats subjected early in life to the MWM also displayed improved behavioral flexibility as compared to rats naïve to the paradigm. Cognitive deficits gradually develop over time and fully emerge in adulthood. Pharmacological modulation of the ubiquitous DAT overexpression overall improves deficits in adult rats, whereas early training decreases later development of behavioral inflexibility. Thus, former training may constitute a preventive avenue that alters some aspects of cognitive deficits resulting from inherent DA abnormalities. Springer US 2022-09-20 2022 /pmc/articles/PMC9616742/ /pubmed/36125729 http://dx.doi.org/10.1007/s12035-022-03029-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Edemann-Callesen, Henriette Glienke, Maximilian Akinola, Esther Olubukola Lieser, Maike Kristin Habelt, Bettina Hadar, Ravit Bernhardt, Nadine Winter, Christine Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter |
title | Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter |
title_full | Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter |
title_fullStr | Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter |
title_full_unstemmed | Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter |
title_short | Former Training Relieves the Later Development of Behavioral Inflexibility in an Animal Model Overexpressing the Dopamine Transporter |
title_sort | former training relieves the later development of behavioral inflexibility in an animal model overexpressing the dopamine transporter |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616742/ https://www.ncbi.nlm.nih.gov/pubmed/36125729 http://dx.doi.org/10.1007/s12035-022-03029-5 |
work_keys_str_mv | AT edemanncallesenhenriette formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT glienkemaximilian formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT akinolaestherolubukola formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT liesermaikekristin formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT habeltbettina formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT hadarravit formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT bernhardtnadine formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter AT winterchristine formertrainingrelievesthelaterdevelopmentofbehavioralinflexibilityinananimalmodeloverexpressingthedopaminetransporter |