Sculpting Dendritic Spines during Initiation and Maintenance of Neuropathic Pain
Affiliation
Univ Arizona, Coll Med, Dept PharmacolUniv Arizona, Ctr Innovat Brain Sci
Univ Arizona, BIO5 Inst
Univ Arizona, Coll Med, Dept Anesthesiol
Issue Date
2020-09-30
Metadata
Show full item recordPublisher
SOC NEUROSCIENCECitation
Stratton, H. J., & Khanna, R. (2020). Sculpting Dendritic Spines during Initiation and Maintenance of Neuropathic Pain. Journal of Neuroscience, 40(40), 7578-7589.Journal
JOURNAL OF NEUROSCIENCERights
Copyright © 2020 the authors.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Accumulating evidence has established a firm role for synaptic plasticity in the pathogenesis of neuropathic pain. Recent advances have highlighted the importance of dendritic spine remodeling in driving synaptic plasticity within the CNS. Identifying the molecular players underlying neuropathic pain induced structural and functional maladaptation is therefore critical to understanding its pathophysiology. This process of dynamic reorganization happens in unique phases that have diverse pathologic underpinnings in the initiation and maintenance of neuropathic pain. Recent evidence suggests that pharmacological targeting of specific proteins during distinct phases of neuropathic pain development produces enhanced antinociception. These findings outline a potential new paradigm for targeted treatment and the development of novel therapies for neuropathic pain. We present a concise review of the role of dendritic spines in neuropathic pain and outline the potential for modulation of spine dynamics by targeting two proteins, srGAP3 and Raci, critically involved in the regulation of the actin cytoskeleton.Note
6 month embargo; published 30 September 2020ISSN
0270-6474EISSN
1529-2401PubMed ID
32998955Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1523/JNEUROSCI.1664-20.2020
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