Synaptic Plasticity from Visual Cortex to Hippocampus: Systems Integration in Spatial Information Processing
Abstract
The adult cerebral cortex possesses the remarkable ability to change its neuronal connectivity through experience, a phenomenon termed "synaptic plasticity." Synaptic plasticity constitutes a cellular mechanism that is thought to underlie information storage and memory formation in the brain, and represents a use-dependent long-lasting increase or decrease in synaptic strength. Recent findings, that the adult visual cortex undergoes dynamic synaptic plasticity that is driven by active visual experience, suggest that it may be involved in information processing that could contribute to memory formation. The visual cortex provides a crucial sensory input to the hippocampus, and is a key component for the creation of spatial memories. An understanding of how visual cortical neurons respond with synaptic plasticity to visual experience, and whether these responses influence the induction of hippocampal plasticity, is fundamental to our understanding of the neuronal mechanisms and functional consequences of visuospatial information processing. In this review, we summarize recent findings with regard to the expression of dynamic synaptic plasticity in the visual cortex and how this plasticity may influence information processing in the hippocampus.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Encoding induces synaptic long-term potentiation (LTP) or long-term depression (LTD) as major forms of learning-induced synaptic plasticity.
“Encoding induces synaptic long-term potentiation (LTP) or long-term depression (LTD) as major forms of learning-induced synaptic plasticity (222,527,616,629,1209).”
From About Sleep's Role in Memory (2013) · cites this paper as [1209]
Cites
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896 · see citing works
Ferrier lecture. Functional architecture of macaque monkey visual cortex
Hubel, D. H., & Wiesel, T. N. (1977) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1977.0085 · Cited by 2,608 · see citing works
Remembering the past to imagine the future: the prospective brain
Schacter, D. L., Addis, D. R., & Buckner, R. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2213 · Cited by 2,394 · see citing works
Regional cerebral blood flow throughout the sleep-wake cycle. An H2(15)O PET study
Braun, A. (1997) · Brain · doi:10.1093/brain/120.7.1173 · Cited by 1,268 · see citing works
Functional neuroanatomy of human rapid-eye-movement sleep and dreaming
Maquet, P., Péters, J.-M., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A., & Franck, G. (1996) · Nature · doi:10.1038/383163a0 · Cited by 1,168 · see citing works
Regulation of Gene Expression in Hippocampal Neurons by Distinct Calcium Signaling Pathways
Bading, H., Ginty, D. D., & Greenberg, M. E. (1993) · Science · doi:10.1126/science.8097060 · Cited by 1,157 · see citing works
Brain areas underlying visual mental imagery and visual perception: an fMRI study
Ganis, G., Thompson, W. L., & Kosslyn, S. M. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.02.012 · Cited by 765 · see citing works
Learning invariance from transformation sequences
Földiák, P. (1991) · Neural Computation · doi:10.1162/neco.1991.3.2.194 · Cited by 661 · cited 1× · see citing works
“It is assumed that this process, which takes place gradually from V1 to TE, obeys the Hebbian learning rule, and includes a short memory trace of preceding neuronal activity (Foldiak 1991; Rolls 1992; Wallis and Rolls 1997).”
BackgroundWhen is early visual cortex activated during visual mental imagery?
Kosslyn, S. M., & Thompson, W. L. (2003) · Psychological Bulletin · doi:10.1037/0033-2909.129.5.723 · Cited by 515 · see citing works
A Specific and Enduring Improvement in Visual Motion Discrimination
Ball, K., & Sekuler, R. (1982) · Science · doi:10.1126/science.7134968 · Cited by 383 · see citing works
Zola‐Morgan, S., Squire, L. R., & Ramus, S. J. (1994) · Hippocampus · doi:10.1002/hipo.450040410 · Cited by 362 · see citing works
Otto, T., & Eichenbaum, H. (1992) · Hippocampus · doi:10.1002/hipo.450020310 · Cited by 232 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works
Visual Salience Affects Performance in a Working Memory Task
Fine, M. S., & Minnery, B. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5503-08.2009 · Cited by 115 · see citing works
Shah, D., Verhoye, M., Van der Linden, A., & D’Hooge, R. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy329 · Cited by 25 · see citing works
Talaei, S. A., Azami, A., & Salami, M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.01.024 · Cited by 10 · see citing works
- Authors
- Tsanov, M., & Manahan-Vaughan, D.
- Affiliations
- Ruhr University Bochum (DE)
- International Graduate School of Neuroscience and Medical Faculty, Department of Experimental Neurophysiology, Medical Faculty, Ruhr University Bochum, Germany,
- ORCID
- Tsanov, Marian
- Venue
- The Neuroscientist
- Publisher
- SAGE Publications
- Published
- 2008-12
- Volume
- 14
- Issue
- 6
- Pages
- 584-597
- ISSN
- 1073-8584 (ISSN-L)
- 1089-4098
- OpenAlex
- W2030881565
- Cited by
- 65
- References
- 12
- Citations by year
- 2025: 6 · 2024: 3 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 6 · 2019: 2 · 2018: 5 · 2017: 5 · 2016: 4 · 2014: 1 · 2013: 2 · 2012: 6
- FWCI
- 2.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Neuroscientist (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- synaptic plasticity, visual cortex, hippocampus, spatial memory, memory formation, visual experience, hippocampal plasticity, system integration, long-term potentiation, long-term depression
- MeSH terms
- Animals, Hippocampus, Humans, Neuronal Plasticity, Neurons, Synapses, Visual Cortex, Visual Pathways
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review