The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Intravenous Brain-Derived Neurotrophic Factor Enhances Poststroke Sensorimotor Recovery and Stimulates Neurogenesis
Open accessAbstract
Background and Purpose— The discovery of spontaneous neuronal replacement in the adult brain has shifted experimental stroke therapies toward a combined approach of preventing neuronal cell death and inducing neuronal plasticity. Brain-derived neurotrophic factor (BDNF) was shown to induce antiapoptotic mechanisms after stroke and to reduce infarct size and secondary neuronal cell death. Moreover, in intact animals, BDNF is a potent stimulator of adult neurogenesis. Methods— The current study analyzed the effects of BDNF on induction of neuronal progenitor cell migration and sensorimotor recovery after cortical photothrombotic stroke. Results— Daily intravenous bolus applications of BDNF during the first 5 days after stroke resulted in significantly improved sensorimotor scores up to 6 weeks. At the structural level, BDNF significantly increased neurogenesis in the dentate gyrus and enhanced migration of subventricular zone progenitor cells to the nearby striatum of the ischemic hemisphere. BDNF treatment could not, however, further stimulate progenitor cell recruitment to the cortex. Conclusions— These findings consolidate the role of BDNF as a modulator of neurogenesis in the brain and as an enhancer of long-term functional neurological outcome after cerebral ischemia.
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Cites
The Rat Brain in Stereotaxic Coordinates
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Neuronal replacement from endogenous precursors in the adult brain after stroke
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Induction of neurogenesis in the neocortex of adult mice
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Induction of reproducible brain infarction by photochemically initiated thrombosis
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BDNF and Activity-Dependent Synaptic Modulation: Figure 1.
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BDNF and 5-HT: a dynamic duo in age-related neuronal plasticity and neurodegenerative disorders
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Cited by
Repairing the human brain after stroke: I. Mechanisms of spontaneous recovery
Cramer, S. C. (2008) · Annals of Neurology · doi:10.1002/ana.21393 · Cited by 875
Early Rehabilitation After Stroke: a Narrative Review
Coleman, E. R., Moudgal, R., Lang, K., Hyacinth, H. I., Awosika, O. O., Kissela, B. M., & Feng, W. (2017) · Current Atherosclerosis Reports · doi:10.1007/s11883-017-0686-6 · Cited by 424
The therapeutic potential of the mesenchymal stem cell secretome in ischaemic stroke
Cunningham, C. J., Redondo-Castro, E., & Allan, S. M. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18776802 · Cited by 242
Neural stem cell therapy for subacute and chronic ischemic stroke
Boese, A. C., Le, Q.-S. E., Pham, D., Hamblin, M. H., & Lee, J.-P. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-018-0913-2 · Cited by 205
Pikula, A., Beiser, A. S., Chen, T. C., Preis, S. R., Vorgias, D., DeCarli, C., Au, R., Kelly-Hayes, M., Kase, C. S., Wolf, P. A., et al. (2013) · Stroke · doi:10.1161/strokeaha.113.001447 · Cited by 200
“Animal studies have established a positive effect of BDNF and VEGF on infarct size and on long-term potentiation, neuronal remodeling, and functional motor recovery after induction of an ischemic brain lesion.(25,26) In addition to being a potent angiogenic Figure.”
Background
Metadata
- Authors
- Schäbitz, W.-R., Steigleder, T., Cooper-Kuhn, C. M., Schwab, S., Sommer, C., Schneider, A., & Kuhn, H. G.
- Venue
- Stroke
- Published
- 2007-07
- Volume
- 38
- Issue
- 7
- Pages
- 2165-2172
- ISSN
- 0039-2499 (ISSN-L)
- 1524-4628
- OpenAlex
- W1967114216
- Cited by
- 441
- References
- 33
- FWCI
- 4.56
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Schäbitz, W.-R., Steigleder, T., Cooper-Kuhn, C. M., Schwab, S., Sommer, C., Schneider, A., & Kuhn, H. G. (2007). Intravenous Brain-Derived Neurotrophic Factor Enhances Poststroke Sensorimotor Recovery and Stimulates Neurogenesis. Stroke. https://doi.org/10.1161/strokeaha.106.477331
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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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