Sangam: A Confluence of Knowledge Streams

Prolonged nerve blockade delays the onset of neuropathic pain

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dc.contributor Harvard University--MIT Division of Health Sciences and Technology
dc.contributor Koch Institute for Integrative Cancer Research at MIT
dc.contributor Langer, Robert
dc.contributor Kohane, Daniel S.
dc.contributor Shankarappa, Sahadev A.
dc.contributor Tsui, Jonathan H.
dc.creator Shankarappa, Sahadev A.
dc.creator Tsui, Jonathan H.
dc.creator Kim, Kristine N.
dc.creator Reznor, Gally
dc.creator Dohlman, Jenny C.
dc.creator Langer, Robert S
dc.creator Kohane, Daniel S
dc.date 2013-03-05T22:16:04Z
dc.date 2013-03-05T22:16:04Z
dc.date 2012-10
dc.date 2012-08
dc.date.accessioned 2023-03-01T18:09:25Z
dc.date.available 2023-03-01T18:09:25Z
dc.identifier 0027-8424
dc.identifier 1091-6490
dc.identifier http://hdl.handle.net/1721.1/77568
dc.identifier Shankarappa, S. A. et al. “Prolonged Nerve Blockade Delays the Onset of Neuropathic Pain.” Proceedings of the National Academy of Sciences 109.43 (2012): 17555–17560. CrossRef. Web.
dc.identifier https://orcid.org/0000-0003-0525-9479
dc.identifier https://orcid.org/0000-0003-4255-0492
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/278964
dc.description Aberrant neuronal activity in injured peripheral nerves is believed to be an important factor in the development of neuropathic pain. Pharmacological blockade of that activity has been shown to mitigate the onset of associated molecular events in the nervous system. However, results in preventing onset of pain behaviors by providing prolonged nerve blockade have been mixed. Furthermore, the experimental techniques used to date to provide that blockade were limited in clinical potential in that they would require surgical implantation. To address these issues, we have used liposomes (SDLs) containing saxitoxin (STX), a site 1 sodium channel blocker, and the glucocorticoid agonist dexamethasone to provide nerve blocks lasting ∼1 wk from a single injection. This formulation is easily injected percutaneously. Animals undergoing spared nerve injury (SNI) developed mechanical allodynia in 1 wk; nerve blockade with a single dose of SDLs (duration of block 6.9 ± 1.2 d) delayed the onset of allodynia by 2 d. Treatment with three sequential SDL injections resulting in a nerve block duration of 18.1 ± 3.4 d delayed the onset of allodynia by 1 mo. This very prolonged blockade decreased activation of astrocytes in the lumbar dorsal horn of the spinal cord due to SNI. Changes in expression of injury-related genes due to SNI in the dorsal root ganglia were not affected by SDLs. These findings suggest that formulations of this kind, which could be easy to apply clinically, can mitigate the development of neuropathic pain.
dc.format application/pdf
dc.language en_US
dc.publisher National Academy of Sciences (U.S.)
dc.relation http://dx.doi.org/10.1073/pnas.1214634109
dc.relation Proceedings of the National Academy of Sciences of the United States of America
dc.rights Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.source PNAS
dc.title Prolonged nerve blockade delays the onset of neuropathic pain
dc.type Article
dc.type http://purl.org/eprint/type/JournalArticle


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