The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Memory Representation within the Parahippocampal Region
Open accessAbstract
The activity of 378 single neurons was recorded from areas of the parahippocampal region (PHR), including the perirhinal and lateral entorhinal cortex, as well as the subiculum, in rats performing an odor-guided delayed nonmatching-to-sample task. Nearly every neuron fired in association with some trial event, and every identifiable trial event or behavior was encoded by neuronal activity in the PHR. The greatest proportion of cells was active during odor sampling, and for many cells, activity during this period was odor selective. In addition, odor memory coding was reflected in two general ways. First, a substantial proportion of cells showed odor-selective activity throughout or at the end of the memory delay period. Second, odor-responsive cells showed odor-selective enhancement or suppression of activity during stimulus repetition in the recognition phase of the task. These data, combined with evidence that the PHR is critical for maintaining odor memories in animals performing the same task, indicate that this cortical region mediates the encoding of specific memory cues, maintains stimulus representations, and supports specific match–nonmatch judgments critical to recognition memory. By contrast, hippocampal neurons do not demonstrate evoked or maintained stimulus-specific codings, and hippocampal damage results in little if any decrement in performance on this task. Thus it becomes increasingly clear that the parahippocampal cortex can support recognition memory independent of the distinct memory functions of the hippocampus itself.
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Cites
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Place units in the hippocampus of the freely moving rat
O'Keefe, J. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90055-8 · Cited by 1,836
The hippocampus—what does it do?
Eichenbaum, H., Otto, T., & Cohen, N. J. (1992) · Behavioral and Neural Biology · doi:10.1016/0163-1047(92)90724-i · Cited by 867
Self-citationA Neural Mechanism for Working and Recognition Memory in Inferior Temporal Cortex
Miller, E. K., Li, L., & Desimone, R. (1991) · Science · doi:10.1126/science.1962197 · Cited by 706
Eichenbaum, H., Kuperstein, M., Fagan, A., & Nagode, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-03-00716.1987 · Cited by 378
Self-citationZola‐Morgan, S., Squire, L. R., & Ramus, S. J. (1994) · Hippocampus · doi:10.1002/hipo.450040410 · Cited by 362
Otto, T., & Eichenbaum, H. (1992) · Hippocampus · doi:10.1002/hipo.450020310 · Cited by 232 · cited 6×
“In the most directly comparable study, Otto and Eichenbaum (1992b) recorded the activity of CA1 neurons from rats performing the same odor-guided cDNMS task used here.”
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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
The role of acetylcholine in learning and memory
Hasselmo, M. E. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.09.002 · Cited by 1,693
The role of phase synchronization in memory processes
Fell, J., & Axmacher, N. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2979 · Cited by 1,620
Lisman, J. E., & Jensen, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.007 · Cited by 1,609
The Hippocampus, Memory, and Place Cells
Eichenbaum, H., Dudchenko, P., Wood, E., Shapiro, M., & Tanila, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)80773-4 · Cited by 1,064
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Metadata
- Authors
- Young, B. J., Otto, T., Fox, G. D., & Eichenbaum, H.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1997-07-01
- Volume
- 17
- Issue
- 13
- Pages
- 5183-5195
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W2169787380
- Cited by
- 372
- References
- 7
- FWCI
- 7.37
- Type
- journal article
- Language
- en
- Open access
- hybrid
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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