Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats

The retrosplenial cortex (RSC) belongs to the spatial memory circuit, but the precise timeline of its involvement and the relation to hippocampal activation have not been sufficiently described. We trained rats in a modified version of the T maze with transparent walls and distant visual cues to ind...

Full description

Bibliographic Details
Main Authors: Rafał Czajkowski, Bartosz Zglinicki, Emilia Rejmak, Witold Konopka
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Brain Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3425/10/11/854
id doaj-6640b7e5ce64493bbcae1c07984600e1
record_format Article
spelling doaj-6640b7e5ce64493bbcae1c07984600e12020-11-25T04:01:06ZengMDPI AGBrain Sciences2076-34252020-11-011085485410.3390/brainsci10110854Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in RatsRafał Czajkowski0Bartosz Zglinicki1Emilia Rejmak2Witold Konopka3Laboratory of Spatial Memory, Nencki Institute of Experimental Biology, 02-093 Warsaw, PolandNeurobiology Center, Nencki Institute of Experimental Biology, 02-093 Warsaw, PolandLaboratory of Neurobiology, BRAINCITY, Nencki Institute of Experimental Biology, 02-093 Warsaw, PolandNeurobiology Center, Nencki Institute of Experimental Biology, 02-093 Warsaw, PolandThe retrosplenial cortex (RSC) belongs to the spatial memory circuit, but the precise timeline of its involvement and the relation to hippocampal activation have not been sufficiently described. We trained rats in a modified version of the T maze with transparent walls and distant visual cues to induce the formation of allocentric spatial memory. We used two distinct salient contexts associated with opposite sequences of turns. Switching between contexts allowed us to test the ability of animals to utilize spatial information. We then applied a CatFISH approach with a probe directed against the <i>Arc</i> immediate early gene in order to visualize the associated memory engrams in the RSC and the hippocampus. After training, rats displayed two strategies to solve the maze, with half of the animals relying on distant spatial cues (allocentric) and the other half using egocentric strategy. Rats that did not utilize the spatial cues showed higher <i>Arc</i> levels in the RSC compared to the allocentric group. The overlap between the two context engrams in the RSC was similar in both groups. These results show differential involvement of the RSC and hippocampus during spatial memory acquisition and point toward their distinct roles in forming the cognitive maps.https://www.mdpi.com/2076-3425/10/11/854retrosplenial cortexhippocampusT mazefluorescence in situ hybridization<i>Arc</i>spatial memory
collection DOAJ
language English
format Article
sources DOAJ
author Rafał Czajkowski
Bartosz Zglinicki
Emilia Rejmak
Witold Konopka
spellingShingle Rafał Czajkowski
Bartosz Zglinicki
Emilia Rejmak
Witold Konopka
Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats
Brain Sciences
retrosplenial cortex
hippocampus
T maze
fluorescence in situ hybridization
<i>Arc</i>
spatial memory
author_facet Rafał Czajkowski
Bartosz Zglinicki
Emilia Rejmak
Witold Konopka
author_sort Rafał Czajkowski
title Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats
title_short Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats
title_full Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats
title_fullStr Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats
title_full_unstemmed Strategy-Specific Patterns of <i>Arc</i> Expression in the Retrosplenial Cortex and Hippocampus during T-Maze Learning in Rats
title_sort strategy-specific patterns of <i>arc</i> expression in the retrosplenial cortex and hippocampus during t-maze learning in rats
publisher MDPI AG
series Brain Sciences
issn 2076-3425
publishDate 2020-11-01
description The retrosplenial cortex (RSC) belongs to the spatial memory circuit, but the precise timeline of its involvement and the relation to hippocampal activation have not been sufficiently described. We trained rats in a modified version of the T maze with transparent walls and distant visual cues to induce the formation of allocentric spatial memory. We used two distinct salient contexts associated with opposite sequences of turns. Switching between contexts allowed us to test the ability of animals to utilize spatial information. We then applied a CatFISH approach with a probe directed against the <i>Arc</i> immediate early gene in order to visualize the associated memory engrams in the RSC and the hippocampus. After training, rats displayed two strategies to solve the maze, with half of the animals relying on distant spatial cues (allocentric) and the other half using egocentric strategy. Rats that did not utilize the spatial cues showed higher <i>Arc</i> levels in the RSC compared to the allocentric group. The overlap between the two context engrams in the RSC was similar in both groups. These results show differential involvement of the RSC and hippocampus during spatial memory acquisition and point toward their distinct roles in forming the cognitive maps.
topic retrosplenial cortex
hippocampus
T maze
fluorescence in situ hybridization
<i>Arc</i>
spatial memory
url https://www.mdpi.com/2076-3425/10/11/854
work_keys_str_mv AT rafałczajkowski strategyspecificpatternsofiarciexpressionintheretrosplenialcortexandhippocampusduringtmazelearninginrats
AT bartoszzglinicki strategyspecificpatternsofiarciexpressionintheretrosplenialcortexandhippocampusduringtmazelearninginrats
AT emiliarejmak strategyspecificpatternsofiarciexpressionintheretrosplenialcortexandhippocampusduringtmazelearninginrats
AT witoldkonopka strategyspecificpatternsofiarciexpressionintheretrosplenialcortexandhippocampusduringtmazelearninginrats
_version_ 1724447712148979712