The honeycomb maze provides a novel test to study hippocampal-dependent spatial navigation
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Authors
Wood, Ruth A
Bauza, Marius
Burton, Stephen
Delekate, Andrea
O'Keefe, John
Publication Date
2018-02-01Journal Title
Nature
ISSN
0028-0836
Publisher
Springer Nature
Volume
554
Pages
102-105
Language
eng
Type
Article
This Version
AM
Metadata
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Wood, R. A., Bauza, M., Krupic, J., Burton, S., Delekate, A., Chan, D., & O'Keefe, J. (2018). The honeycomb maze provides a novel test to study hippocampal-dependent spatial navigation. Nature, 554 102-105. https://doi.org/10.1038/nature25433
Abstract
Here we describe the honeycomb maze, a behavioural paradigm for the study of spatial navigation in rats. The maze consists of 37 platforms that can be raised or lowered independently. Place navigation requires an animal to go to a goal platform from any of several start platforms via a series of sequential choices. For each, the animal is confined to a raised platform and allowed to choose between two of the six adjacent platforms, the correct one being the platform with the smallest angle to the goal-heading direction. Rats learn rapidly and their choices are influenced by three factors: the angle between the two choice platforms, the distance from the goal, and the angle between the correct platform and the direction of the goal. Rats with hippocampal damage are impaired in learning and their performance is affected by all three factors. The honeycomb maze represents a marked improvement over current spatial navigation tests, such as the Morris water maze1,2,3, because it controls the choices of the animal at each point in the maze, provides the ability to assess knowledge of the goal direction from any location, enables the identification of factors influencing task performance and provides the possibility for concomitant single-cell recording.
Sponsorship
This work was supported by grants from the Wellcome Trust and the Gatsby Charitable Foundation to J.O. R.A.W. is an MRC Clinical Research Training Fellow, J.K. is a Wellcome Trust/Royal Society Sir Henry Dale Fellow and is supported by the Kavli Foundation Dream Team project and the Isaac Newton Trust. D.C. is funded by the Cambridge NIHR Biomedical Research Centre and by the Wellcome Trust.
Identifiers
External DOI: https://doi.org/10.1038/nature25433
This record's URL: https://www.repository.cam.ac.uk/handle/1810/275793
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