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Medial temporal lobe activation during encoding and retrieval of novel face‐name pairs
Open accessAbstract
The human medial temporal lobe (MTL) is known to be involved in declarative memory, yet the exact contributions of the various MTL structures are not well understood. In particular, the data as to whether the hippocampal region is preferentially involved in the encoding and/or retrieval of associative memory have not allowed for a consensus concerning its specific role. To investigate the role of the hippocampal region and the nearby MTL cortical areas in encoding and retrieval of associative versus non‐associative memories, we used functional magnetic resonance imaging (fMRI) to measure brain activity during learning and later recognition testing of novel face‐name pairs. We show that there is greater activity for successful encoding of associative information than for non‐associative information in the right hippocampal region, as well as in the left amygdala and right parahippocampal cortex. Activity for retrieval of associative information was greater than for non‐associative information in the right hippocampal region also, as well as in the left perirhinal cortex, right entorhinal cortex, and right parahippocampal cortex. The implications of these data for a clear functional distinction between the hippocampal region and the MTL cortical structures are discussed. © 2004 Wiley‐Liss, Inc.
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AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913
Tulving, E. (1985) · Canadian Psychology / Psychologie canadienne · doi:10.1037/h0080017 · Cited by 4,638
Episodic memory, amnesia, and the hippocampal–anterior thalamic axis
Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879
Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory
Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746
(2000) · doi:10.1093/oso/9780195122657.001.0001 · Cited by 1,340
The global record of memory in hippocampal neuronal activity
Wood, E. R., Dudchenko, P. A., & Eichenbaum, H. (1999) · Nature · doi:10.1038/17605 · Cited by 707
The Neuropsychology of Memory: Parallel Findings in Humans and Nonhuman Primatesa
ZOLA‐MORGAN, S., & SQUIRE, L. R. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb48905.x · Cited by 318
Cited by
Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680
Self-citationThe Medial Temporal Lobe and Recognition Memory
Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580
Eichenbaum (2004) · doi:10.1016/j.neuron.2004.08.028 · Cited by 1,464
Item, context and relational episodic encoding in humans
Davachi, L. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.10.012 · Cited by 1,138
Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375
Schlichting, M. L., Mumford, J. A., & Preston, A. R. (2015) · Nature Communications · doi:10.1038/ncomms9151 · Cited by 381
Ezzyat, Y., & Davachi, L. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.042 · Cited by 321
The Hippocampus and Imagining the Future: Where Do We Stand?
Addis, D. R., & Schacter, D. L. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00173 · Cited by 285
Rapid Encoding of New Memories by Individual Neurons in the Human Brain
Ison, M. J., Quian Quiroga, R., & Fried, I. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.016 · Cited by 184
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
Gordon, A. M., Rissman, J., Kiani, R., & Wagner, A. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht194 · Cited by 173
False memories with age: neural and cognitive underpinnings
Devitt, A. L., & Schacter, D. L. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.08.030 · Cited by 171
The role of the hippocampus in memory and mental construction
Sheldon, S., & Levine, B. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13006 · Cited by 155
A role for the hippocampus in encoding simulations of future events
Martin, V. C., Schacter, D. L., Corballis, M. C., & Addis, D. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105816108 · Cited by 144
Tsukiura, T., & Cabeza, R. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.03.013 · Cited by 90
Neural mechanisms of social influence
Mason, M. F., Dyer, R., & Norton, M. I. (2009) · Organizational Behavior and Human Decision Processes · doi:10.1016/j.obhdp.2009.04.001 · Cited by 93
exercise influence on hippocampal function: possible involvement of orexin-A
Chieffi, S., Messina, G., Villano, I., Messina, A., Esposito, M., Monda, V., Valenzano, A., Moscatelli, F., Esposito, T., Carotenuto, M., et al. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00085 · Cited by 90
Spontaneous thought as an unconstrained memory process
Mildner, J. N., & Tamir, D. I. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.09.001 · Cited by 83
Distributed learning enhances relational memory consolidation
Litman, L., & Davachi, L. (2008) · Learning & Memory · doi:10.1101/lm.1132008 · Cited by 81
Gaesser, B., Spreng, R. N., McLelland, V. C., Addis, D. R., & Schacter, D. L. (2013) · Hippocampus · doi:10.1002/hipo.22152 · Cited by 78
Stress Impairs Episodic Retrieval by Disrupting Hippocampal and Cortical Mechanisms of Remembering
Gagnon, S. A., Waskom, M. L., Brown, T. I., & Wagner, A. D. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy162 · Cited by 69
Escaping the Past: Contributions of the Hippocampus to Future Thinking and Imagination
Schacter, D. L., Addis, D. R., & Szpunar, K. K. (2017) · The Hippocampus from Cells to Systems · doi:10.1007/978-3-319-50406-3_14 · Cited by 54
Yamashita, K.-I., Hirose, S., Kunimatsu, A., Aoki, S., Chikazoe, J., Jimura, K., Masutani, Y., Abe, O., Ohtomo, K., Miyashita, Y., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1328-09.2009 · Cited by 51
Chen, Y.-C., Ton That, V., Ugonna, C., Liu, Y., Nadel, L., & Chou, Y.-H. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2113778119 · Cited by 29
Remembering and imagining differentially engage the hippocampus: a multivariate fMRI investigation
Kirwan, C. B., Ashby, S. R., & Nash, M. I. (2014) · Cognitive Neuroscience · doi:10.1080/17588928.2014.933203 · Cited by 19
Self-citationAmer, T., & Davachi, L. (2022) · doi:10.31234/osf.io/32egy · Cited by 3
Metadata
- Authors
- Kirwan, C. B., & Stark, C. E. L.
- Venue
- Hippocampus
- Publisher
- Wiley
- Published
- 2004-01
- Volume
- 14
- Issue
- 7
- Pages
- 919-930
- ISSN
- 1050-9631 (ISSN-L)
- 1098-1063
- OpenAlex
- W2092135096
- Cited by
- 326
- References
- 7
- FWCI
- 9.12
- Type
- journal article
- Language
- en
- Open access
- bronze
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