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Retrosplenial cortex

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Retrosplenial cortex
Medial surface of the brain with Brodmann's areas numbered.
Details
Identifiers
LatinRegio retrosplenialis
NeuroNames2436, 1802
Anatomical terms of neuroanatomy

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

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]

References

  1. ^ a b Vogt, B. A. (1976-09-01). "Retrosplenial cortex in the rhesus monkey: a cytoarchitectonic and Golgi study". The Journal of Comparative Neurology. 169 (1): 63–97. doi:10.1002/cne.901690105. ISSN 0021-9967. PMID 821976.
  2. ^ a b c d Vann, Seralynne D.; Aggleton, John P.; Maguire, Eleanor A. (8 October 2009). "What does the retrosplenial cortex do?". Nature Reviews Neuroscience. 10 (11): 792–802. doi:10.1038/nrn2733. PMID 19812579.
  3. ^ notes, K. Brodmann ; translated with editorial; Garey, an introduction by Laurence J. (2006). Brodmann's Localisation in the cerebral cortex the principles of comparative localisation in the cerebral cortex based on cytoarchitectonics (3rd ed.). New York: Springer. ISBN 978-0-387-26919-1.{{cite book}}: CS1 maint: multiple names: authors list (link)
  4. ^ a b Chen, Longtang L.; Lin, Lie-Huey; Green, Edward J.; Barnes, Carol A.; McNaughton, Bruce L. (September 1994). "Head-direction cells in the rat posterior cortex". Experimental Brain Research. 101 (1): 8–23. doi:10.1007/BF00243212. PMID 7843305.
  5. ^ a b Cho, J; Sharp, PE (February 2001). "Head direction, place, and movement correlates for cells in the rat retrosplenial cortex". Behavioral neuroscience. 115 (1): 3–25. doi:10.1037/0735-7044.115.1.3. PMID 11256450.
  6. ^ Alexander, Andrew S.; Nitz, Douglas A. (2015-08-01). "Retrosplenial cortex maps the conjunction of internal and external spaces". Nature Neuroscience. 18 (8): 1143–1151. doi:10.1038/nn.4058. ISSN 1546-1726. PMID 26147532.
  7. ^ Spreng, R. Nathan; Mar, Raymond A.; Kim, Alice S. N. (March 2009). "The Common Neural Basis of Autobiographical Memory, Prospection, Navigation, Theory of Mind, and the Default Mode: A Quantitative Meta-analysis". Journal of Cognitive Neuroscience. 21 (3): 489–510. doi:10.1162/jocn.2008.21029. PMID 18510452.
  8. ^ Pothuizen, Helen H. J.; Davies, Moira; Albasser, Mathieu M.; Aggleton, John P.; Vann, Seralynne D. (September 2009). "Granular and dysgranular retrosplenial cortices provide qualitatively different contributions to spatial working memory: evidence from immediate-early gene imaging in rats". European Journal of Neuroscience. 30 (5): 877–888. doi:10.1111/j.1460-9568.2009.06881.x. PMID 19712100.
  9. ^ Czajkowski, R.; Jayaprakash, B.; Wiltgen, B.; Rogerson, T.; Guzman-Karlsson, M. C.; Barth, A. L.; Trachtenberg, J. T.; Silva, A. J. (27 May 2014). "Encoding and storage of spatial information in the retrosplenial cortex". Proceedings of the National Academy of Sciences. 111 (23): 8661–8666. doi:10.1073/pnas.1313222111.
  10. ^ Yoder, Ryan M.; Clark, Benjamin J.; Taube, Jeffrey S. (November 2011). "Origins of landmark encoding in the brain". Trends in Neurosciences. 34 (11): 561–571. doi:10.1016/j.tins.2011.08.004. PMID 21982585.
  11. ^ Auger, Stephen D.; Mullally, Sinéad L.; Maguire, Eleanor A.; Baker, Chris I. (17 August 2012). "Retrosplenial Cortex Codes for Permanent Landmarks". PLoS ONE. 7 (8): e43620. Bibcode:2012PLoSO...743620A. doi:10.1371/journal.pone.0043620. PMC 3422332. PMID 22912894.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  12. ^ Auger, Stephen D.; Maguire, Eleanor A. (November 2013). "Assessing the mechanism of response in the retrosplenial cortex of good and poor navigators". Cortex. 49 (10): 2904–2913. doi:10.1016/j.cortex.2013.08.002. PMID 24012136.
  13. ^ Committeri, Giorgia; Galati, Gaspare; Paradis, Anne-Lise; Pizzamiglio, Luigi; Berthoz, Alain; LeBihan, Denis (November 2004). "Reference Frames for Spatial Cognition: Different Brain Areas are Involved in Viewer-, Object-, and Landmark-Centered Judgments About Object Location". Journal of Cognitive Neuroscience. 16 (9): 1517–1535. doi:10.1162/0898929042568550. PMID 15601516.
  14. ^ Galati, Gaspare; Pelle, Gina; Berthoz, Alain; Committeri, Giorgia (26 February 2010). "Multiple reference frames used by the human brain for spatial perception and memory". Experimental Brain Research. 206 (2): 109–120. doi:10.1007/s00221-010-2168-8. PMID 20186405.
  15. ^ Byrne, Patrick; Becker, Suzanna; Burgess, Neil (2007). "Remembering the past and imagining the future: A neural model of spatial memory and imagery". Psychological Review. 114 (2): 340–375. doi:10.1037/0033-295X.114.2.340. PMID 17500630.
  16. ^ Maguire, Eleanor A.; Valentine, Elizabeth R.; Wilding, John M.; Kapur, Narinder (16 December 2002). "Routes to remembering: the brains behind superior memory". Nature Neuroscience. 6 (1): 90–95. doi:10.1038/nn988. PMID 12483214.
  17. ^ Destrade, C; Ott, T (2 December 1982). "Is a retrosplenial (cingulate) pathway involved in the mediation of high frequency hippocampal rhythmical slow activity (theta)?". Brain Research. 252 (1): 29–37. doi:10.1016/0006-8993(82)90975-1. PMID 6293657.
  18. ^ Foster, B. L.; Kaveh, A.; Dastjerdi, M.; Miller, K. J.; Parvizi, J. (19 June 2013). "Human Retrosplenial Cortex Displays Transient Theta Phase Locking with Medial Temporal Cortex Prior to Activation during Autobiographical Memory Retrieval". Journal of Neuroscience. 33 (25): 10439–10446. doi:10.1523/JNEUROSCI.0513-13.2013. PMID 23785155.
  19. ^ Valenstein, E; Bowers, D; Verfaellie, M; Heilman, KM; Day, A; Watson, RT (December 1987). "Retrosplenial amnesia". Brain : a journal of neurology. 110 (6): 1631–46. doi:10.1093/brain/110.6.1631. PMID 3427404.
  20. ^ Pengas, George; Hodges, John R.; Watson, Peter; Nestor, Peter J. (January 2010). "Focal posterior cingulate atrophy in incipient Alzheimer's disease". Neurobiology of Aging. 31 (1): 25–33. doi:10.1016/j.neurobiolaging.2008.03.014. PMID 18455838.
  21. ^ Pengas, George; Williams, Guy B.; Acosta-Cabronero, Julio; Ash, Tom W. J.; Hong, Young T.; Izquierdo-Garcia, David; Fryer, Tim D.; Hodges, John R.; Nestor, Peter J. (2012). "Retrosplenial Cortex (BA 29) Volumes in Behavioral Variant Frontotemporal Dementia and Alzheimer's Disease". Frontiers in Aging Neuroscience. 4. doi:10.3389/fnagi.2012.00017.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  22. ^ Tan, Rachel H.; Wong, Stephanie; Hodges, John R.; Halliday, Glenda M.; Hornberger, Michael (2013). "Retrosplenial Cortex (BA 29) Volumes in Behavioral Variant Frontotemporal Dementia and Alzheimer's Disease". Dementia and Geriatric Cognitive Disorders. 35 (3–4): 177–182. doi:10.1159/000346392. PMID 23406695.
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