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Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze

In the water maze, mice are trained to navigate to an escape platform located below the water's surface, and spatial learning is most commonly evaluated in a probe test in which the platform is removed from the pool. While contemporary tracking software provides precise positional information o...

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Autores principales: Maei, Hamid R., Zaslavsky, Kirill, Wang, Afra H., Yiu, Adelaide P., Teixeira, Cátia M., Josselyn, Sheena A., Frankland, Paul W.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2802531/
https://www.ncbi.nlm.nih.gov/pubmed/20057926
http://dx.doi.org/10.3389/neuro.07.033.2009
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author Maei, Hamid R.
Zaslavsky, Kirill
Wang, Afra H.
Yiu, Adelaide P.
Teixeira, Cátia M.
Josselyn, Sheena A.
Frankland, Paul W.
author_facet Maei, Hamid R.
Zaslavsky, Kirill
Wang, Afra H.
Yiu, Adelaide P.
Teixeira, Cátia M.
Josselyn, Sheena A.
Frankland, Paul W.
author_sort Maei, Hamid R.
collection PubMed
description In the water maze, mice are trained to navigate to an escape platform located below the water's surface, and spatial learning is most commonly evaluated in a probe test in which the platform is removed from the pool. While contemporary tracking software provides precise positional information of mice for the duration of the probe test, existing performance measures (e.g., percent quadrant time, platform crossings) fail to exploit fully the richness of this positional data. Using the concept of entropy (H), here we develop a new measure that considers both how focused the search is and the degree to which searching is centered on the former platform location. To evaluate how H performs compared to existing measures of water maze performance we compiled five separate databases, containing more than 1600 mouse probe tests. Random selection of individual trials from respective databases then allowed us to simulate experiments with varying sample and effect sizes. Using this Monte Carlo-based method, we found that H outperformed existing measures in its ability to detect group differences over a range of sample or effect sizes. Additionally, we validated the new measure using three models of experimentally induced hippocampal dysfunction: (1) complete hippocampal lesions, (2) genetic deletion of αCaMKII, a gene implicated in hippocampal behavioral and synaptic plasticity, and (3) a mouse model of Alzheimer's disease. Together, these data indicate that H offers greater sensitivity than existing measures, most likely because it exploits the richness of the precise positional information of the mouse throughout the probe test.
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spelling pubmed-28025312010-01-07 Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze Maei, Hamid R. Zaslavsky, Kirill Wang, Afra H. Yiu, Adelaide P. Teixeira, Cátia M. Josselyn, Sheena A. Frankland, Paul W. Front Integr Neurosci Neuroscience In the water maze, mice are trained to navigate to an escape platform located below the water's surface, and spatial learning is most commonly evaluated in a probe test in which the platform is removed from the pool. While contemporary tracking software provides precise positional information of mice for the duration of the probe test, existing performance measures (e.g., percent quadrant time, platform crossings) fail to exploit fully the richness of this positional data. Using the concept of entropy (H), here we develop a new measure that considers both how focused the search is and the degree to which searching is centered on the former platform location. To evaluate how H performs compared to existing measures of water maze performance we compiled five separate databases, containing more than 1600 mouse probe tests. Random selection of individual trials from respective databases then allowed us to simulate experiments with varying sample and effect sizes. Using this Monte Carlo-based method, we found that H outperformed existing measures in its ability to detect group differences over a range of sample or effect sizes. Additionally, we validated the new measure using three models of experimentally induced hippocampal dysfunction: (1) complete hippocampal lesions, (2) genetic deletion of αCaMKII, a gene implicated in hippocampal behavioral and synaptic plasticity, and (3) a mouse model of Alzheimer's disease. Together, these data indicate that H offers greater sensitivity than existing measures, most likely because it exploits the richness of the precise positional information of the mouse throughout the probe test. Frontiers Research Foundation 2009-12-04 /pmc/articles/PMC2802531/ /pubmed/20057926 http://dx.doi.org/10.3389/neuro.07.033.2009 Text en Copyright © 2009 Maei, Zaslavsky, Wang, Yiu, Teixeira, Josselyn and Frankland. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Maei, Hamid R.
Zaslavsky, Kirill
Wang, Afra H.
Yiu, Adelaide P.
Teixeira, Cátia M.
Josselyn, Sheena A.
Frankland, Paul W.
Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze
title Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze
title_full Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze
title_fullStr Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze
title_full_unstemmed Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze
title_short Development and Validation of a Sensitive Entropy-Based Measure for the Water Maze
title_sort development and validation of a sensitive entropy-based measure for the water maze
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2802531/
https://www.ncbi.nlm.nih.gov/pubmed/20057926
http://dx.doi.org/10.3389/neuro.07.033.2009
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