The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Local Generation and Propagation of Ripples along the Septotemporal Axis of the Hippocampus
Open accessAbstract
A topographical relationship exists between the septotemporal segments of the hippocampus and their entorhinal–neocortical targets, but the physiological organization of activity along the septotemporal axis is poorly understood. We recorded sharp-wave ripple patterns in rats during sleep from the entire septotemporal axis of the CA1 pyramidal layer. Qualitatively similar ripples emerged at all levels. From the local seed, ripples traveled septally or temporally at a speed of ∼0.35 m/s, and the spatial spread depended on ripple magnitude. Ripples propagated smoothly across the septal and intermediate segments of the hippocampus, but ripples in the temporal segment often remained isolated. These findings show that ripples can combine information from the septal and intermediate hippocampus and transfer integrated signals downstream. In contrast, ripples that emerged in the temporal pole broadcast largely independent information to their cortical and subcortical targets.
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Reverse replay of behavioural sequences in hippocampal place cells during the awake state
Foster, D. J., & Wilson, M. A. (2006) · Nature · doi:10.1038/nature04587 · Cited by 1,727
Two-stage model of memory trace formation: A role for “noisy” brain states
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Self-citationCoordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669
Selective suppression of hippocampal ripples impairs spatial memory
Girardeau, G., Benchenane, K., Wiener, S. I., Buzsáki, G., & Zugaro, M. B. (2009) · Nature Neuroscience · doi:10.1038/nn.2384 · Cited by 1,560
Self-citationTwo cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377
Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo
Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345
Self-citationMemory of sequential experience in the hippocampus during slow wave sleep
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GABA-containing neurons in the septum control inhibitory interneurons in the hippocampus
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Forward and reverse hippocampal place-cell sequences during ripples
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Cited by
Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759
Self-citationScaling Brain Size, Keeping Timing: Evolutionary Preservation of Brain Rhythms
Buzsáki, G., Logothetis, N., & Singer, W. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.002 · Cited by 886
Self-citationThe hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation
Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430
Reactivations of emotional memory in the hippocampus-amygdala system during sleep
Girardeau, G., Inema, I., & Buzsáki, G. (2017) · Nature Neuroscience · doi:10.1038/nn.4637 · Cited by 266
Self-citationMemory trace replay: The shaping of memory consolidation by neuromodulation
Atherton, L. A., Dupret, D., & Mellor, J. R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.004 · Cited by 180
Metadata
- Authors
- Patel, J., Schomburg, E. W., Berényi, A., Fujisawa, S., & Buzsáki, G.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2013-10-23
- Volume
- 33
- Issue
- 43
- Pages
- 17029-17041
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W1970443910
- Cited by
- 172
- References
- 27
- FWCI
- 4.38
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Patel, J., Schomburg, E. W., Berényi, A., Fujisawa, S., & Buzsáki, G. (2013). Local Generation and Propagation of Ripples along the Septotemporal Axis of the Hippocampus. The Journal of Neuroscience. https://doi.org/10.1523/jneurosci.2036-13.2013
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
