Retrosplenial Cortical Neurons Encode Navigational Cues, Trajectories and Reward Locations During Goal Directed Navigation

The retrosplenial cortex (RSC) plays an important role in memory and spatial navigation. It shares functional similarities with the hippocampus, including the presence of place fields and lesion-induced impairments in spatial navigation, and the RSC is an important source of visual-spatial input to...

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Published inCerebral cortex (New York, N.Y. 1991) Vol. 27; no. 7; pp. 3713 - 3723
Main Authors Vedder, Lindsey C., Miller, Adam M. P., Harrison, Marc B., Smith, David M.
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 01.07.2017
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Abstract The retrosplenial cortex (RSC) plays an important role in memory and spatial navigation. It shares functional similarities with the hippocampus, including the presence of place fields and lesion-induced impairments in spatial navigation, and the RSC is an important source of visual-spatial input to the hippocampus. Recently, the RSC has been the target of intense scrutiny among investigators of human memory and navigation. fMRI and lesion data suggest an RSC role in the ability to use landmarks to navigate to goal locations. However, no direct neurophysiological evidence of encoding navigational cues has been reported so the specific RSC contribution to spatial cognition has been uncertain. To examine this, we trained rats on a T-maze task in which the reward location was explicitly cued by a flashing light and we recorded RSC neurons as the rats learned. We found that RSC neurons rapidly encoded the light cue. Additionally, RSC neurons encoded the reward and its location, and they showed distinct firing patterns along the left and right trajectories to the goal. These responses may provide key information for goal-directed navigation, and the loss of these signals may underlie navigational impairments in subjects with RSC damage.
AbstractList The retrosplenial cortex (RSC) plays an important role in memory and spatial navigation. It shares functional similarities with the hippocampus, including the presence of place fields and lesion-induced impairments in spatial navigation, and the RSC is an important source of visual-spatial input to the hippocampus. Recently, the RSC has been the target of intense scrutiny among investigators of human memory and navigation. fMRI and lesion data suggest an RSC role in the ability to use landmarks to navigate to goal locations. However, no direct neurophysiological evidence of encoding navigational cues has been reported so the specific RSC contribution to spatial cognition has been uncertain. To examine this, we trained rats on a T-maze task in which the reward location was explicitly cued by a flashing light and we recorded RSC neurons as the rats learned. We found that RSC neurons rapidly encoded the light cue. Additionally, RSC neurons encoded the reward and its location, and they showed distinct firing patterns along the left and right trajectories to the goal. These responses may provide key information for goal-directed navigation, and the loss of these signals may underlie navigational impairments in subjects with RSC damage.
Author Harrison, Marc B.
Vedder, Lindsey C.
Smith, David M.
Miller, Adam M. P.
AuthorAffiliation 1 Department of Psychology , Cornell University , Ithaca, NY 14853 , USA
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Snippet The retrosplenial cortex (RSC) plays an important role in memory and spatial navigation. It shares functional similarities with the hippocampus, including the...
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StartPage 3713
SubjectTerms Action Potentials - physiology
Analysis of Variance
Animals
Cerebral Cortex - cytology
Cues
Functional Laterality
Goals
Male
Maze Learning - physiology
Neurons - physiology
Original
Rats
Rats, Long-Evans
Reward
Spatial Navigation - physiology
Title Retrosplenial Cortical Neurons Encode Navigational Cues, Trajectories and Reward Locations During Goal Directed Navigation
URI https://www.ncbi.nlm.nih.gov/pubmed/27473323
https://www.proquest.com/docview/1826737092
https://pubmed.ncbi.nlm.nih.gov/PMC6059095
Volume 27
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