Contribution of egocentric spatial memory to place navigation of rats in the Morris water maze
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8864044
DOI
10.1016/0166-4328(95)00240-5
PII: 0166432895002405
Knihovny.cz E-zdroje
- MeSH
- bludiště - učení fyziologie MeSH
- kognice fyziologie MeSH
- krysa rodu Rattus MeSH
- motorické dovednosti fyziologie MeSH
- orientace fyziologie MeSH
- paměť fyziologie MeSH
- podněty MeSH
- přeučení fyziologie MeSH
- světlo MeSH
- tma MeSH
- vnímání prostoru fyziologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Place navigation in the Morris water maze can be directed by memory of the target coordinates relative to remote landmarks (allocentric) or by the memory of the start-goal route (egocentric). When the start and goal positions remain constant and visual cues are eliminated by darkness, memory of the route may become decisive. This assumption was tested in 10 male hooded rats using an infrared television tracking system allowing navigation training in the dark. In Expt. 1, these animals were trained to swim in the dark from the start at the S rim of the pool to the goal position in the center of the NW quadrant of the pool. Mean escape latencies decreased from 47 s initially to 16 s during the 24 daily sessions. Another group of 10 male hooded rats learned the same task in the light. Mean escape latencies decreased from 20 s initially to 5 s during 4 daily sessions. In Expt. 2, possible allocentric location of the target was tested in the same rats by rotating both the start and goal positions by 90 degrees counterclockwise (i.e., to E-SW and later to N-SE). Mean escape latency during 5 days after the first rotation increased to 24 s, but returned back to the asymptotic level of 18 s after the second rotation. The same change of the start and goal position (from S-NW to E-SW) in the light only increased escape latency in the first session. In Expt. 3, both the goal position and route direction were changed to N-SW. Surprisingly, the animals rapidly acquired a new heading angle at the start and mean escape latencies were not significantly changed. It is concluded that overtrained place navigation in darkness can be easily changed to a new direction.
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