Harnessing neuroplasticity for clinical applications
Open accessAbstract
Neuroplasticity can be defined as the ability of the nervous system to respond to intrinsic or extrinsic stimuli by reorganizing its structure, function and connections. Major advances in the understanding of neuroplasticity have to date yielded few established interventions. To advance the translation of neuroplasticity research towards clinical applications, the National Institutes of Health Blueprint for Neuroscience Research sponsored a workshop in 2009. Basic and clinical researchers in disciplines from central nervous system injury/stroke, mental/addictive disorders, paediatric/developmental disorders and neurodegeneration/ageing identified cardinal examples of neuroplasticity, underlying mechanisms, therapeutic implications and common denominators. Promising therapies that may enhance training-induced cognitive and motor learning, such as brain stimulation and neuropharmacological interventions, were identified, along with questions of how best to use this body of information to reduce human disability. Improved understanding of adaptive mechanisms at every level, from molecules to synapses, to networks, to behaviour, can be gained from iterative collaborations between basic and clinical researchers. Lessons can be gleaned from studying fields related to plasticity, such as development, critical periods, learning and response to disease. Improved means of assessing neuroplasticity in humans, including biomarkers for predicting and monitoring treatment response, are needed. Neuroplasticity occurs with many variations, in many forms, and in many contexts. However, common themes in plasticity that emerge across diverse central nervous system conditions include experience dependence, time sensitivity and the importance of motivation and attention. Integration of information across disciplines should enhance opportunities for the translation of neuroplasticity and circuit retraining research into effective clinical therapies.
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tDCS combined with cognitive training may yield larger and long-lasting functional improvements that modify the impaired system.
“yielding larger and long-lasting functional improvements that modify the impaired system (Cramer et al., 2011).”
From Cognitive Neuroscience of Attention Deficit Hyperactivity Disorder (ADHD) and Its Clinical Translation (2018) · cites this paper as Cramer et al., 2011
The Non-invasive brain stimulation section (page unavailable) says that combining neuromodulation with a behavioural intervention may increase its efficacy and that stimulation effects can outlast stimulation. The Cognitive training section describes a goal of driving adaptive changes in dysfunctional neural systems. The paper does not establish that tDCS combined specifically with cognitive training yields larger, long-lasting functional improvements. (LLM, conf=0.85)
Experimental — accuracy not yet measuredExternal factors change the ways our brains operate, including neuronal structures and functions, as indicated by neuroplasticity studies.
“while these same external factors change the ways our brains operate, including neuronal structures and functions, as indicated by studies into neuroplasticity (Fuchs and Flügge 2014;Cramer et al. 2011).”
From Authenticity and Love Drugs: Insights from Psychedelic Therapy (2026) · cites this paper as Cramer et al. 2011
In the nervous system, integrins are essential molecules for neuroplasticity.
“In the nervous system, integrins are essential molecules for neuroplasticity, i.e. the ability to adapt to internal and external stimuli by reorganizing its structure, function and connections [49].”
From Gene expression profiles underlying aggressive behavior in the prefrontal cortex of cattle (2021) · cites this paper as [49]
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- Authors
- Cramer, S. C., Sur, M., Dobkin, B. H., O'Brien, C., Sanger, T. D., Trojanowski, J. Q., Rumsey, J. M., Hicks, R., Cameron, J., Chen, D., Chen, W. G., Cohen, L. G., deCharms, C., Duffy, C. J., Eden, G. F., Fetz, E. E., Filart, R., Freund, M., Grant, S. J., Haber, S., Kalivas, P. W., Kolb, B., Kramer, A. F., Lynch, M., Mayberg, H. S., McQuillen, P. S., Nitkin, R., Pascual-Leone, A., Reuter-Lorenz, P., Schiff, N., Sharma, A., Shekim, L., Stryker, M., Sullivan, E. V., & Vinogradov, S.
- Affiliations
- University of California, Irvine (US)
- University of California, Los Angeles (US)
- University of Southern California (US)
- National Institutes of Health (US)
- Oregon Health & Science University (US)
- Omneuron (United States) (US)
- National Institute of Mental Health (US)
- Medical University of South Carolina (US)
- University of Lethbridge (CA)
- University of Illinois Urbana-Champaign (US)
- Emory University (US)
- University of Colorado Boulder (US)
- University of California, San Francisco (US)
- Corresponding author
- Cramer, S. C.
- ORCID
- Venue
- Brain
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-04-10
- Volume
- 134
- Issue
- 6
- Pages
- 1591-1609
- ISSN
- 0006-8950 (ISSN-L)
- 1460-2156
- PMC
- PMC3102236
- OpenAlex
- W2107022859
- Cited by
- 1,259
- References
- 228
- Citations by year
- 2026: 92 · 2025: 116 · 2024: 93 · 2023: 89 · 2022: 99 · 2021: 93 · 2020: 130 · 2019: 80 · 2018: 53 · 2017: 79 · 2016: 69 · 2015: 69 · 2014: 85 · 2013: 58 · 2012: 43
- FWCI
- 34.98
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Brain (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- U.S. Department of Health and Human Services
- Pfizer
- GlaxoSmithKline
- Gilead Sciences
- National Institutes of Health
- Allergan
- National Institute on Alcohol Abuse and Alcoholism (R37AA010723, K05AA017168)
- National Institute on Aging (R01AG036682, R37AG025667)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD069381)
- Topics
- Life Sciences › Neuroscience › Neurology › Transcranial Magnetic Stimulation Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- neuroplasticity, clinical translation, brain stimulation, stroke, central nervous system injury, mental illness, addiction, neurodegeneration, aging, experience-dependent plasticity, critical period, treatment response biomarkers, disability reduction
- MeSH terms
- Aging, Animals, Brain Diseases, Cognition Disorders, Humans, Neuronal Plasticity, Recovery of Function, Stroke, Biomedical Research
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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.
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