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Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells
OBJECTIVE: The active place avoidance task (APA) is a behavioural task used to assess learning and memory in rodents. This task relies on the hippocampus, a region of the cerebral cortex capable of generating new neurons from neural stem cells. In this study, to gain further insight into the behavio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080370/ https://www.ncbi.nlm.nih.gov/pubmed/30081965 http://dx.doi.org/10.1186/s13104-018-3652-7 |
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author | Zalucki, Oressia Harkins, Danyon Harris, Lachlan Burne, Thomas H. J. Gronostajski, Richard M. Piper, Michael |
author_facet | Zalucki, Oressia Harkins, Danyon Harris, Lachlan Burne, Thomas H. J. Gronostajski, Richard M. Piper, Michael |
author_sort | Zalucki, Oressia |
collection | PubMed |
description | OBJECTIVE: The active place avoidance task (APA) is a behavioural task used to assess learning and memory in rodents. This task relies on the hippocampus, a region of the cerebral cortex capable of generating new neurons from neural stem cells. In this study, to gain further insight into the behavioural phenotype of mice deficient in the transcription factor Nfix, a gene expressed by adult neural stem cells, we examined learning and memory parameters from the APA task that were not published in our original investigation. We analysed time to first and second shock, maximum path and time of shock avoidance, number of entries into the shock zone and time spent in the shock zone. We also assessed performance in the APA task based on sex. RESULTS: We found mice deficient in Nfix displayed decreased latency to second shock compared to the control mice. Nfix deficient mice entered the shock zone more frequently and also spent more time in the shock zone. Our data provides further insights into the memory deficits evident in Nfix mutant mice, indicating these mice have a memory retrieval problem and may employ a different navigation strategy in the APA task. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3652-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6080370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60803702018-08-09 Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells Zalucki, Oressia Harkins, Danyon Harris, Lachlan Burne, Thomas H. J. Gronostajski, Richard M. Piper, Michael BMC Res Notes Research Note OBJECTIVE: The active place avoidance task (APA) is a behavioural task used to assess learning and memory in rodents. This task relies on the hippocampus, a region of the cerebral cortex capable of generating new neurons from neural stem cells. In this study, to gain further insight into the behavioural phenotype of mice deficient in the transcription factor Nfix, a gene expressed by adult neural stem cells, we examined learning and memory parameters from the APA task that were not published in our original investigation. We analysed time to first and second shock, maximum path and time of shock avoidance, number of entries into the shock zone and time spent in the shock zone. We also assessed performance in the APA task based on sex. RESULTS: We found mice deficient in Nfix displayed decreased latency to second shock compared to the control mice. Nfix deficient mice entered the shock zone more frequently and also spent more time in the shock zone. Our data provides further insights into the memory deficits evident in Nfix mutant mice, indicating these mice have a memory retrieval problem and may employ a different navigation strategy in the APA task. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3652-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-06 /pmc/articles/PMC6080370/ /pubmed/30081965 http://dx.doi.org/10.1186/s13104-018-3652-7 Text en © The Author(s) 2018 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 | Research Note Zalucki, Oressia Harkins, Danyon Harris, Lachlan Burne, Thomas H. J. Gronostajski, Richard M. Piper, Michael Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells |
title | Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells |
title_full | Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells |
title_fullStr | Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells |
title_full_unstemmed | Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells |
title_short | Analysis of hippocampal-dependent learning and memory behaviour in mice lacking Nfix from adult neural stem cells |
title_sort | analysis of hippocampal-dependent learning and memory behaviour in mice lacking nfix from adult neural stem cells |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080370/ https://www.ncbi.nlm.nih.gov/pubmed/30081965 http://dx.doi.org/10.1186/s13104-018-3652-7 |
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