What does the retrosplenial cortex do?

Vann, Seralynne D.; Aggleton, John P.; Maguire, Eleanor A.

doi:10.1038/nrn2733

Cited by 1,409Memory and Neural MechanismsSpatial Cognition and NavigationMemory Processes and Influences

What does the retrosplenial cortex do?

Vann, Seralynne D., Aggleton, John P., Maguire, Eleanor A.·2009·Nature Reviews Neuroscience

DOI 10.1038/nrn2733

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Abstract

The past decade has seen a transformation in research on the retrosplenial cortex (RSC). This cortical area has emerged as a key member of a core network of brain regions that underpins a range of cognitive functions, including episodic memory, navigation, imagination and planning for the future. It is now also evident that the RSC is consistently compromised in the most common neurological disorders that impair memory. Here we review advances on multiple fronts, most notably in neuroanatomy, animal studies and neuroimaging, that have highlighted the importance of the RSC for cognition, and consider why specifying its precise functions remains problematic.

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Both retrosplenial damage and hippocampal damage can cause anterograde amnesia.
“This outcome is to be expected as both retrosplenial damage and hippocampal damage can cause anterograde amnesia (Spiers et al., 2001; Valenstein et al., 1987; Vann et al., 2009)”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as Vann et al., 2009
RSC has been previously implicated in spatial navigation and spatial memory.
“This region has been previously implicated in spatial navigation13, 22 and spatial memory14, 23.”
From Anchoring the neural compass: coding of local spatial reference frames in human medial parietal lobe (2014) · cites this paper as [14]
There is striking overlap among brain regions involved in retrieval of autobiographical memories, imagination of novel events, and navigation.
“Much recent interest has focused on the striking overlap among brain regions involved in the retrieval of autobiographical memories, the imagination of novel events, and navigation14, 47, 48.”
From Anchoring the neural compass: coding of local spatial reference frames in human medial parietal lobe (2014) · cites this paper as [14]
Retrosplenial cortex is thought to support integration and translation between egocentric spatial representations in posterior parietal cortex and allocentric spatial representations in the MTL.
“Retrosplenial cortex is thought to support integration and translation between egocentric spatial representations in posterior parietal cortex and allocentric spatial representations in the MTL (71), and these processes are recruited to a greater extent when spatial context needs to be updated and manipulated (72).”
From Neural mechanisms of reactivation-induced updating that enhance and distort memory (2013) · cites this paper as [72]

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Directional Disorientation Following Left Retrosplenial Hemorrhage: a Case Report with FMRI Studies
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Retrosplenial cortex lesions of area Rgb (but not of area Rga) impair spatial learning and memory in the rat
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Cingulate Cortex
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Macaque monkey retrosplenial cortex: I. Three-dimensional and cytoarchitectonic organization
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Electrical activity of the cingulate cortex. II. Cholinergic modulation
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Full Scenes produce more activation than Close-up Scenes and Scene-Diagnostic Objects in parahippocampal and retrosplenial cortex: An fMRI study
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Hippocampal, retrosplenial, and prefrontal hypoactivity in a model of diencephalic amnesia: Evidence towards an interdependent subcortical‐cortical memory network
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Involvement of the retrosplenial cortex in processing multiple conditioned stimuli.
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Pure topographic disorientation: A distinctive syndrome with varied localization
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Memory impairment and spatial disorientation following a left retrosplenial lesion
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Retrosplenial cortex lesions impair water maze strategies learning or spatial place learning depending on prior experience of the rat
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(1997) · doi:10.1002/(sici)1098-1063(1997)7:4

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Authors: Vann, S. D., Aggleton, J. P., & Maguire, E. A.
Affiliations: Cardiff University (GB)
Wellcome Centre for Human Neuroimaging (GB)
Corresponding author: Vann, Seralynne D.
ORCID: Vann, Seralynne D.
Aggleton, John P.
Maguire, Eleanor A.
Venue: Nature Reviews Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2009-10-08
Volume: 10
Issue: 11
Pages: 792-802
ISSN: 1471-003X (ISSN-L)
1471-0048
DOI: 10.1038/nrn2733
OpenAlex: W1991490575
Cited by: 1,409
References: 144
Citations by year: 2026: 70 · 2025: 118 · 2024: 97 · 2023: 92 · 2022: 106 · 2021: 94 · 2020: 97 · 2019: 87 · 2018: 109 · 2017: 76 · 2016: 89 · 2015: 83 · 2014: 69 · 2013: 80 · 2012: 50
FWCI: 3.51
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature reviews. Neuroscience (publishedVersion)
PubMed (publishedVersion)
ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
UCL Discovery (University College London) (submittedVersion)
Funders: Wellcome Trust (084218)
National Institutes of Health
Biotechnology and Biological Sciences Research Council (BB/D002001/1, BB/B501955/1)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Keywords: retrosplenial cortex, episodic memory, spatial navigation, scene construction, perspective taking, memory disorders, cognitive function, neuroanatomy, neuroimaging, animal studies
MeSH terms: Animals, Cerebral Cortex, Cognition, Gyrus Cinguli, Humans, Nerve Net, Anterior Thalamic Nuclei

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