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CORTICAL PLASTICITY: From Synapses to Maps
Abstract
It has been clear for almost two decades that cortical representations in adult animals are not fixed entities, but rather, are dynamic and are continuously modified by experience. The cortex can preferentially allocate area to represent the particular peripheral input sources that are proportionally most used. Alterations in cortical representations appear to underlie learning tasks dependent on the use of the behaviorally important peripheral inputs that they represent. The rules governing this cortical representational plasticity following manipulations of inputs, including learning, are increasingly well understood. In parallel with developments in the field of cortical map plasticity, studies of synaptic plasticity have characterized specific elementary forms of plasticity, including associative long-term potentiation and long-term depression of excitatory postsynaptic potentials. Investigators have made many important strides toward understanding the molecular underpinnings of these fundamental plasticity processes and toward defining the learning rules that govern their induction. The fields of cortical synaptic plasticity and cortical map plasticity have been implicitly linked by the hypothesis that synaptic plasticity underlies cortical map reorganization. Recent experimental and theoretical work has provided increasingly stronger support for this hypothesis. The goal of the current paper is to review the fields of both synaptic and cortical map plasticity with an em…
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“These theoretical predictions are entirely consistent with empirical and computational characterisations of plasticity [56],[57].”
From Hierarchical Models in the Brain (2008) · cites this paper as [56]
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Neurophysiological mechanisms involved in language learning in adults
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“…during the last decade, the concepts of neural plasticity, neurogeneration and brain repair have been carefully redefined and the emergent picture of the adult learning brain is more dynamic, open and encouraging than the previous views (Buonomano & Merzenich 1998; Bruer 2003; De Felipe 2006).”
ResultLong-term modification of cortical synapses improves sensory perception
Froemke, R. C., Carcea, I., Barker, A. J., Yuan, K., Seybold, B., Martins, A. R. O., Zaika, N., Bernstein, H. L., Wachs, M. A., Levis, P. A., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3274 · Cited by 218
Self-citationBook Review: How Do We Tell Time?
Buonomano, D. V., & Karmarkar, U. R. (2002) · The Neuroscientist · doi:10.1177/107385840200800109 · Cited by 218
Self-citationInhibitory and Excitatory Spike-Timing-Dependent Plasticity in the Auditory Cortex
D’amour, J. A., & Froemke, R. C. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.014 · Cited by 210
“…adjustments of excitatory synaptic strength are believed to be a major mechanism by which cortical networks adapt to the statistics of sensory input, over a range of timescales from seconds to days (Buonomano and Merzenich, 1998; Froemke and Martins, 2011; Martin et al., 2000; McGaugh 2000).”
BackgroundA neurobiological approach to the cognitive deficits of psychiatric disorders
Etkin, A., Gyurak, A., & O'Hara, R. M. (2013) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2013.15.4/aetkin · Cited by 212
A brain perspective on language mechanisms: from discrete neuronal ensembles to serial order
Friedemann Pulvermüller, A. (2002) · Progress in Neurobiology · doi:10.1016/s0301-0082(02)00014-x · Cited by 210
The application of errorless learning to aphasic disorders: A review of theory and practice
Fillingham, J., Hodgson, C., Sage, K., & Ralph, M. L. (2003) · Neuropsychological Rehabilitation · doi:10.1080/09602010343000020 · Cited by 152
Selective disorders of reading?
Patterson, K. E., & Ralph, M. A. L. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80033-6 · Cited by 207
A resilience framework for promoting stable remission from depression
Waugh, C. E., & Koster, E. H. W. (2015) · Clinical Psychology Review · doi:10.1016/j.cpr.2014.05.004 · Cited by 202
“Meditation is a form of mental training that takes advantage of the brain’s inherent neural plasticity – changes in neural structure and functioning in response to environmental demands (Buonomano & Merzenich, 1998).”
BackgroundTwo Cortical Areas Mediate Multisensory Integration in Superior Colliculus Neurons
Jiang, W., Wallace, M. T., Jiang, H., Vaughan, J. W., & Stein, B. E. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.506 · Cited by 205
Naturalistic experience transforms sensory maps in the adult cortex of caged animals
Polley, D. B., Kvašňák, E., & Frostig, R. D. (2004) · Nature · doi:10.1038/nature02469 · Cited by 205
Metadata
- Authors
- Buonomano, D. V., & Merzenich, M. M.
- Affiliations
- University of California, Los Angeles (US)
- University of California, San Francisco (US)
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 1998-03
- Volume
- 21
- Issue
- 1
- Pages
- 149-186
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2158935809
- Cited by
- 2,083
- References
- 192
- Citations by year
- 2026: 21 · 2025: 27 · 2024: 43 · 2023: 40 · 2022: 45 · 2021: 58 · 2020: 49 · 2019: 73 · 2018: 67 · 2017: 61 · 2016: 61 · 2015: 78 · 2014: 72 · 2013: 95 · 2012: 98
- FWCI
- 8.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (10414)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- cortical plasticity, synaptic plasticity, long-term potentiation, long-term depression, excitatory postsynaptic potentials, learning rules
- MeSH terms
- Animals, Brain Mapping, Cerebral Cortex, Neuronal Plasticity, Synapses
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