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Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis
We here show that living in a stimulus‐rich environment (ENR) improves water maze learning with respect to specific key indicators that in previous loss‐of‐function experiments have been shown to rely on adult hippocampal neurogenesis. Analyzing the strategies employed by mice to locate the hidden p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049654/ https://www.ncbi.nlm.nih.gov/pubmed/26311488 http://dx.doi.org/10.1002/hipo.22520 |
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author | Garthe, Alexander Roeder, Ingo Kempermann, Gerd |
author_facet | Garthe, Alexander Roeder, Ingo Kempermann, Gerd |
author_sort | Garthe, Alexander |
collection | PubMed |
description | We here show that living in a stimulus‐rich environment (ENR) improves water maze learning with respect to specific key indicators that in previous loss‐of‐function experiments have been shown to rely on adult hippocampal neurogenesis. Analyzing the strategies employed by mice to locate the hidden platform in the water maze revealed that ENR facilitated task acquisition by increasing the probability to use effective search strategies. ENR also enhanced the animals’ behavioral flexibility, when the escape platform was moved to a new location. Treatment with temozolomide, which is known to reduce adult neurogenesis, abolished the effects of ENR on both acquisition and flexibility, while leaving other aspects of water maze learning untouched. These characteristic effects and interdependencies were not seen in parallel experiments with voluntary wheel running (RUN), a second pro‐neurogenic behavioral stimulus. Since the histological assessment of adult neurogenesis is by necessity an end‐point measure, the levels of neurogenesis over the course of the experiment can only be inferred and the present study focused on behavioral parameters as analytical endpoints. Although the correlation of physical activity with precursor cell proliferation and of learning and the survival of new neurons is well established, how the specific functional effects described here relate to dynamic changes in the stem cell niche remains to be addressed. Nevertheless, our findings support the hypothesis that adult neurogenesis is a critical mechanism underlying the beneficial effects of leading an active live, rich in experiences. © 2015 The Authors Hippocampus Published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-5049654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50496542016-10-06 Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis Garthe, Alexander Roeder, Ingo Kempermann, Gerd Hippocampus Research Articles We here show that living in a stimulus‐rich environment (ENR) improves water maze learning with respect to specific key indicators that in previous loss‐of‐function experiments have been shown to rely on adult hippocampal neurogenesis. Analyzing the strategies employed by mice to locate the hidden platform in the water maze revealed that ENR facilitated task acquisition by increasing the probability to use effective search strategies. ENR also enhanced the animals’ behavioral flexibility, when the escape platform was moved to a new location. Treatment with temozolomide, which is known to reduce adult neurogenesis, abolished the effects of ENR on both acquisition and flexibility, while leaving other aspects of water maze learning untouched. These characteristic effects and interdependencies were not seen in parallel experiments with voluntary wheel running (RUN), a second pro‐neurogenic behavioral stimulus. Since the histological assessment of adult neurogenesis is by necessity an end‐point measure, the levels of neurogenesis over the course of the experiment can only be inferred and the present study focused on behavioral parameters as analytical endpoints. Although the correlation of physical activity with precursor cell proliferation and of learning and the survival of new neurons is well established, how the specific functional effects described here relate to dynamic changes in the stem cell niche remains to be addressed. Nevertheless, our findings support the hypothesis that adult neurogenesis is a critical mechanism underlying the beneficial effects of leading an active live, rich in experiences. © 2015 The Authors Hippocampus Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-02 2015-09-15 /pmc/articles/PMC5049654/ /pubmed/26311488 http://dx.doi.org/10.1002/hipo.22520 Text en © 2015 The Authors Hippocampus Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Garthe, Alexander Roeder, Ingo Kempermann, Gerd Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
title | Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
title_full | Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
title_fullStr | Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
title_full_unstemmed | Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
title_short | Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
title_sort | mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049654/ https://www.ncbi.nlm.nih.gov/pubmed/26311488 http://dx.doi.org/10.1002/hipo.22520 |
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