Retrosplenial cortex

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Retrosplenial cortex
Gray727-Brodman.png
Medial surface of the brain with Brodmann's areas numbered.
Details
Latin Regio retrosplenialis
Identifiers
NeuroNames ancil-111
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Anatomical terms of neuroanatomy
[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).|edit on Wikidata]]]

The retrosplenial cortex (RSC) is a cortical area in the brain, located posteriorly (towards the back) and comprising Brodmann areas 29 and 30 [1].The region's name refers to its anatomical location immediately behind the splenium of the corpus callosum in primates, although in rodents it is located more towards the brain surface and is relatively larger. Its function is currently not well understood, but its location close to visual areas and also to the hippocampal spatial/memory system suggest it may have a role in mediating between perceptual and memory functions.[2]

Anatomy

Lua error in package.lua at line 80: module 'strict' not found. There is a large amount of variation in the region's size across different species. In humans it comprises roughly 0.3% of the entire cortical surface whereas in rabbits it is at least 10%[3] and in rats it extends for more than half the cerebrum dorso-ventrally, making it one of the largest cortical regions.[2] On the basis of its microscopic cellular structure it is divided into dysgranular (area 30) and granular (area 29) regions.[1]

The retrosplenial cortex has dense reciprocal projections with the visual cortex, postsubiculum (also known as dorsal presubiculum) and with anterior thalamic nuclei and the hippocampus.

Neurophysiology

Neurophysiological studies of retrosplenial cortex have mainly been done in rats. In rodents, around 8.5% of neurons in the retrosplenial cortex are head direction cells while other neurons have correlates with movement parameters such as running speed, and there is also evidence of weak spatial coding.[4][5] Much of the observed activity has been found to be conjunctive (reflecting more than one parameter at once).[4][5] A recent study of rats running on a long linear maze found complex patterns of activity reflecting conjunctions between position on the track, position on the track within the room at large and whether the animal was turning left or right.[6]

Function

In humans, fMRI studies implicate the retrosplenial cortex in a wide range of cognitive functions including episodic memory, navigation, imagining future events and processing scenes more generally.[7][2] Rodent studies suggest the region is important for using surrounding visual cues to carry out these tasks.[8][9][10] Retrosplenial cortex is particularly responsive to permanent, non-moving environmental landmarks[11][12] and is also implicated in using them to make spatial judgements.[13][14]

It has also been suggested that retrosplenial cortex may translate between egocentric (self-centred) and allocentric (world-centred) spatial information, based upon its anatomical location between the hippocampus (where there are allocentric place cell representations) and the parietal lobe (which integrates egocentric sensory information).[15]

Competitors in the World Memory Championships are able to perform outstanding feats of memory and show increased fMRI activation in their retrosplenial cortex than normal controls when doing so.[16] This is thought to be due to their use of a spatial learning strategy or mnemonic device known as the method of loci.

The region also displays slow-wave theta rhythmicity[17] and when people retrieve autobiographical memories, there is theta band interaction between the retrosplenial cortex and the medial temporal lobe.[18]

Pathology

The retrosplenial cortex is one of several brain areas that produces both an anterograde and retrograde amnesia when damaged.[19] People with lesions involving the retrosplenial cortex also display a form of topographical disorientation whereby they can recognise and identify environmental landmarks, but are unable to use them to orientate themselves.[2]

The retrosplenial cortex is one of the first regions to undergo pathological changes in Alzheimer's disease and its prodromal phase of mild cognitive impairment.[20][21][22]

Gallery

References

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