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Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice

Spatial navigation is a fundamental capability necessary in everyday life to locate food, social partners, and shelter. It results from two very different strategies: (1) place learning which enables for flexible way finding and (2) response learning that leads to a more rigid “route following.” Des...

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Autores principales: Kleinknecht, Karl R., Bedenk, Benedikt T., Kaltwasser, Sebastian F., Grünecker, Barbara, Yen, Yi-Chun, Czisch, Michael, Wotjak, Carsten T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530747/
https://www.ncbi.nlm.nih.gov/pubmed/23293591
http://dx.doi.org/10.3389/fnbeh.2012.00087
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author Kleinknecht, Karl R.
Bedenk, Benedikt T.
Kaltwasser, Sebastian F.
Grünecker, Barbara
Yen, Yi-Chun
Czisch, Michael
Wotjak, Carsten T.
author_facet Kleinknecht, Karl R.
Bedenk, Benedikt T.
Kaltwasser, Sebastian F.
Grünecker, Barbara
Yen, Yi-Chun
Czisch, Michael
Wotjak, Carsten T.
author_sort Kleinknecht, Karl R.
collection PubMed
description Spatial navigation is a fundamental capability necessary in everyday life to locate food, social partners, and shelter. It results from two very different strategies: (1) place learning which enables for flexible way finding and (2) response learning that leads to a more rigid “route following.” Despite the importance of knockout techniques that are only available in mice, little is known about mice' flexibility in spatial navigation tasks. Here we demonstrate for C57BL6/N mice in a water-cross maze (WCM) that only place learning enables spatial flexibility and relearning of a platform position, whereas response learning does not. This capability depends on an intact hippocampal formation, since hippocampus lesions by ibotenic acid (IA) disrupted relearning. In vivo manganese-enhanced magnetic resonance imaging revealed a volume loss of ≥60% of the hippocampus as a critical threshold for relearning impairments. In particular the changes in the left ventral hippocampus were indicative of relearning deficits. In summary, our findings establish the importance of hippocampus-dependent place learning for spatial flexibility and provide a first systematic analysis on spatial flexibility in mice.
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spelling pubmed-35307472013-01-04 Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice Kleinknecht, Karl R. Bedenk, Benedikt T. Kaltwasser, Sebastian F. Grünecker, Barbara Yen, Yi-Chun Czisch, Michael Wotjak, Carsten T. Front Behav Neurosci Neuroscience Spatial navigation is a fundamental capability necessary in everyday life to locate food, social partners, and shelter. It results from two very different strategies: (1) place learning which enables for flexible way finding and (2) response learning that leads to a more rigid “route following.” Despite the importance of knockout techniques that are only available in mice, little is known about mice' flexibility in spatial navigation tasks. Here we demonstrate for C57BL6/N mice in a water-cross maze (WCM) that only place learning enables spatial flexibility and relearning of a platform position, whereas response learning does not. This capability depends on an intact hippocampal formation, since hippocampus lesions by ibotenic acid (IA) disrupted relearning. In vivo manganese-enhanced magnetic resonance imaging revealed a volume loss of ≥60% of the hippocampus as a critical threshold for relearning impairments. In particular the changes in the left ventral hippocampus were indicative of relearning deficits. In summary, our findings establish the importance of hippocampus-dependent place learning for spatial flexibility and provide a first systematic analysis on spatial flexibility in mice. Frontiers Media S.A. 2012-12-27 /pmc/articles/PMC3530747/ /pubmed/23293591 http://dx.doi.org/10.3389/fnbeh.2012.00087 Text en Copyright © 2012 Kleinknecht, Bedenk, Kaltwasser, Grünecker, Yen, Czisch and Wotjak. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Kleinknecht, Karl R.
Bedenk, Benedikt T.
Kaltwasser, Sebastian F.
Grünecker, Barbara
Yen, Yi-Chun
Czisch, Michael
Wotjak, Carsten T.
Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice
title Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice
title_full Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice
title_fullStr Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice
title_full_unstemmed Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice
title_short Hippocampus-dependent place learning enables spatial flexibility in C57BL6/N mice
title_sort hippocampus-dependent place learning enables spatial flexibility in c57bl6/n mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530747/
https://www.ncbi.nlm.nih.gov/pubmed/23293591
http://dx.doi.org/10.3389/fnbeh.2012.00087
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