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The Parahippocampus Subserves Topographical Learning in Man
Abstract
The hippocampus has been proposed as the site of neural representation of large-scale environmental space, based upon the identification of place cells (neurons with receptive fields for current position in the environment) within the rat hippocampus and the demonstration that hippocampal lesions impair place learning in the rat. The inability to identify place cells within the monkey hippocampus and the observation that unilateral hippocampal lesions do not selectively impair topographic behavior in humans suggest that alternate regions may subserve this function in man. To examine the contribution of the hippocampus and adjacent medial-temporal lobe structures to topographic learning in the human, a 'virtual' maze was used as a task environment during functional magnetic resonance imaging studies. During the learning and recall of topographic information, medial-temporal activity was confined to the para- hippocampal gyri. This activity accords well with the lesion site known to produce topographical disorientation in humans. Activity was also observed in cortical areas known to project to the parahippocampus and previously proposed to contribute to a network subserving spatially guided behavior.
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Cites
Statistical parametric maps in functional imaging: A general linear approach
Friston, K. J., Holmes, A. P., Worsley, K. J., Poline, J. ‐., Frith, C. D., & Frackowiak, R. S. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020402 · Cited by 9,688
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340
Cited by
Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies
Cabeza, R., & Nyberg, L. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137585 · Cited by 3,598
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401
Bar, M. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1476 · Cited by 1,613
Cellular networks underlying human spatial navigation
Ekstrom, A. D., Kahana, M. J., Caplan, J. B., Fields, T. A., Isham, E. A., Newman, E. L., & Fried, I. (2003) · Nature · doi:10.1038/nature01964 · Cited by 1,425
A new neural framework for visuospatial processing
Kravitz, D. J., Saleem, K. S., Baker, C. I., & Mishkin, M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3008 · Cited by 1,325
Blood, A. J., Zatorre, R. J., Bermudez, P., & Evans, A. C. (1999) · Nature Neuroscience · doi:10.1038/7299 · Cited by 1,097
The cognitive map in humans: spatial navigation and beyond
Epstein, R. A., Patai, E. Z., Julian, J. B., & Spiers, H. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4656 · Cited by 921
Moscovitch, M., Rosenbaum, R. S., Gilboa, A., Addis, D. R., Westmacott, R., Grady, C., McAndrews, M. P., Levine, B., Black, S., Winocur, G., et al. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00421.x · Cited by 893
Separating the brain regions involved in recollection and familiarity in recognition memory
Yonelinas, A. P., Otten, L. J., Shaw, K. N., & Rugg, M. D. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.5295-04.2005 · Cited by 813
Topographical disorientation: a synthesis and taxonomy
Aguirre, G. K. (1999) · Brain · doi:10.1093/brain/122.9.1613 · Cited by 772
Self-citationHuman theta oscillations exhibit task dependence during virtual maze navigation
Kahana, M. J., Sekuler, R., Caplan, J. B., Kirschen, M., & Madsen, J. R. (1999) · Nature · doi:10.1038/21645 · Cited by 649
The neuropsychology of 3-D space.
Previc, F. H. (1998) · Psychological Bulletin · doi:10.1037/0033-2909.124.2.123 · Cited by 604
Bohbot, V. D., Kalina, M., Stepankova, K., Spackova, N., Petrides, M., & Nadel, L. (1998) · Neuropsychologia · doi:10.1016/s0028-3932(97)00161-9 · Cited by 516
A temporoparietal and prefrontal network for retrieving the spatial context of lifelike events
Burgess, N., Maguire, E. A., Spiers, H. J., & O'Keefe, J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0806 · Cited by 502
Episodic memory in normal aging and Alzheimer disease: Insights from imaging and behavioral studies
Tromp, D., Dufour, A., Lithfous, S., Pebayle, T., & Després, O. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.08.006 · Cited by 390
Memory for places learned long ago is intact after hippocampal damage
Teng, E., & Squire, L. R. (1999) · Nature · doi:10.1038/23276 · Cited by 372
Thoughts, behaviour, and brain dynamics during navigation in the real world
Spiers, H. J., & Maguire, E. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.037 · Cited by 371
Where am I now? Distinct roles for parahippocampal and retrosplenial cortices in place recognition
Epstein, R. A., Parker, W. E., & Feiler, A. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0799-07.2007 · Cited by 331
Ekstrom, A. D., Arnold, A. E. G. F., & Iaria, G. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00803 · Cited by 263
Rosenbaum, R. S., Ziegler, M., Winocur, G., Grady, C. L., & Moscovitch, M. (2004) · Hippocampus · doi:10.1002/hipo.10218 · Cited by 258
Kondo, H., Saleem, K. S., & Price, J. L. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20796 · Cited by 236
Age differences in the formation and use of cognitive maps
Iaria, G., Palermo, L., Committeri, G., & Barton, J. J. S. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.08.040 · Cited by 231
Weniger, G., Ruhleder, M., Lange, C., Wolf, S., & Irle, E. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.12.031 · Cited by 204
Distances between real-world locations are represented in the human hippocampus
Morgan, L. K., MacEvoy, S. P., Aguirre, G. K., & Epstein, R. A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4667-10.2011 · Cited by 203
Fenske, M. J., Aminoff, E., Gronau, N., & Bar, M. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)55001-0 · Cited by 190
Neural correlates of virtual route reCognition in congenital blindness
Kupers, R., Chebat, D. R., Madsen, K. H., Paulson, O. B., & Ptito, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006199107 · Cited by 187
Berkovich-Ohana, A., Dor-Ziderman, Y., Glicksohn, J., & Goldstein, A. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00912 · Cited by 171
Can Taichi Reshape the Brain? A Brain Morphometry Study
Wei, G.-X., Xu, T., Fan, F.-M., Dong, H.-M., Jiang, L.-L., Li, H.-J., Yang, Z., Luo, J., & Zuo, X.-N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061038 · Cited by 152
Visual Scene Processing in Familiar and Unfamiliar Environments
Epstein, R. A., Higgins, J. S., Jablonski, K., & Feiler, A. M. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00003.2007 · Cited by 153
Neural foundations of emerging route knowledge in complex spatial environments
Wolbers, T., Weiller, C., & Büchel, C. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.06.013 · Cited by 146
Anterior hippocampus and goal-directed spatial decision making
Viard, A., Doeller, C. F., Hartley, T., Bird, C. M., & Burgess, N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4640-10.2011 · Cited by 144
Dissociable networks involved in spatial and temporal order source retrieval
Ekstrom, A. D., Copara, M. S., Isham, E. A., Wang, W.-C., & Yonelinas, A. P. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.033 · Cited by 135
Lesions Affecting the Parahippocampal Cortex Yield Spatial Memory Deficits in Humans
Ploner, C. J. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1211 · Cited by 132
Abstract Representations of Location and Facing Direction in the Human Brain
Vass, L. K., & Epstein, R. A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3873-12.2013 · Cited by 131
Wirth, S., Baraduc, P., Planté, A., Pinède, S., & Duhamel, J.-R. (2017) · PLOS Biology · doi:10.1371/journal.pbio.2001045 · Cited by 129
Neural evidence supports a novel framework for spatial navigation
Chrastil, E. R. (2013) · Psychonomic Bulletin & Review · doi:10.3758/s13423-012-0351-6 · Cited by 126
Detecting Consciousness: A Unique Role for Neuroimaging
Owen, A. M. (2013) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143729 · Cited by 122
The neuroscience of remote spatial memory: A tale of two cities
Spiers, H. J., & Maguire, E. A. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.056 · Cited by 117
Functional Neuroanatomy of the Medial Temporal Lobe Memory System
SUZUKI, W., & AMARAL, D. (2004) · Cortex · doi:10.1016/s0010-9452(08)70958-4 · Cited by 111
Influence of attentional demands on the processing of emotional facial expressions in the amygdala
Silvert, L., Lepsien, J., Fragopanagos, N., Goolsby, B., Kiss, M., Taylor, J. G., Raymond, J. E., Shapiro, K. L., Eimer, M., & Nobre, A. C. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.023 · Cited by 104
Reagh, Z. M., & Ranganath, C. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.04.050 · Cited by 83
Hanlon, C. A., Owens, M. M., Joseph, J. E., Zhu, X., George, M. S., Brady, K. T., & Hartwell, K. J. (2016) · Addiction Biology · doi:10.1111/adb.12171 · Cited by 82
Reward-based spatial learning in unmedicated adults with obsessive-compulsive disorder
Marsh, R., Tau, G. Z., Wang, Z., Huo, Y., Liu, G., Hao, X., Packard, M. G., Peterson, B. S., & Simpson, H. B. (2015) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2014.13121700 · Cited by 53
Activation of the hippocampal complex during tactile maze solving in congenitally blind subjects
Gagnon, L., Schneider, F. C., Siebner, H. R., Paulson, O. B., Kupers, R., & Ptito, M. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.03.022 · Cited by 45
Diminution of context association memory structure in subjects with subjective cognitive decline
Fan, L., Lai, Y., Chen, T., Hsu, Y., Chen, P., Huang, K., Cheng, T., Tseng, W. I., Hua, M., Chen, Y., et al. (2018) · Human Brain Mapping · doi:10.1002/hbm.24022 · Cited by 40
Sjölie, D., Bodin, K., Elgh, E., Eriksson, J., Janlert, L.-E., & Nyberg, L. (2010) · Proceedings of the SIGCHI Conference on Human Factors in Computing Systems · doi:10.1145/1753326.1753454 · Cited by 19
Metadata
- Authors
- Aguirre, G. K., Detre, J. A., Alsop, D. C., & D'Esposito, M.
- Venue
- Cerebral Cortex
- Publisher
- Oxford University Press (OUP)
- Published
- 1996
- Volume
- 6
- Issue
- 6
- Pages
- 823-829
- ISSN
- 1047-3211 (ISSN-L)
- 1460-2199
- OpenAlex
- W2082259851
- Cited by
- 622
- References
- 2
- FWCI
- 13.49
- Type
- journal article
- Language
- en
- Open access
- closed
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