Literature DB >> 19559391

Sodium channel expression and localization at demyelinated sites in painful human dental pulp.

Michael A Henry1, Songjiang Luo, Benjamin D Foley, Rachael S Rzasa, Lonnie R Johnson, S Rock Levinson.   

Abstract

UNLABELLED: The expression of sodium channels (NaCh(s)) change after inflammatory and nerve lesions, and this change has been implicated in the generation of pain states. Here we examine NaCh expression within nerve fibers from normal and painful extracted human teeth with special emphasis on their localization within large accumulations, like those seen at nodes of Ranvier. Pulpal tissue sections from normal wisdom teeth and from teeth with large carious lesions associated with severe and spontaneous pain were double-stained with pan-specific NaCh antibody and caspr (paranodal protein used to visualize nodes of Ranvier) antibody, while additional sections were triple-stained with NaCh, caspr and myelin basic protein (MBP) antibodies. Z-series of images were obtained with the confocal microscope and evaluated with NIH ImageJ software to quantify the density and size of NaCh accumulations, and to characterize NaCh localization at caspr-identified typical and atypical nodal sites. Although the results showed variability in the overall density and size of NaCh accumulations in painful samples, a common finding included the remodeling of NaChs at atypical nodal sites. This remodeling of NaChs included prominent NaCh expression within nerve regions that showed a selective loss of MBP staining in a pattern consistent with a demyelinating process. PERSPECTIVE: This study identifies the remodeling of NaChs at demyelinated sites within the painful human dental pulp and suggests that the contribution of NaChs to spontaneous pulpal pain generation may be dependant not only on total NaCh density but may also be related to NaCh expression at atypical nodal sites.

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Year:  2009        PMID: 19559391      PMCID: PMC2750027          DOI: 10.1016/j.jpain.2009.01.264

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.820


  31 in total

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3.  Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels.

Authors:  S Poliak; L Gollan; R Martinez; A Custer; S Einheber; J L Salzer; J S Trimmer; P Shrager; E Peles
Journal:  Neuron       Date:  1999-12       Impact factor: 17.173

4.  Increased sodium channel immunofluorescence at myelinated and demyelinated sites following an inflammatory and partial axotomy lesion of the rat infraorbital nerve.

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6.  Changed distribution of sodium channels along demyelinated axons.

Authors:  J D England; F Gamboni; S R Levinson; T E Finger
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Authors:  S Dugandzija-Novaković; A G Koszowski; S R Levinson; P Shrager
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Authors:  Songjiang Luo; Griffin M Perry; S Rock Levinson; Michael A Henry
Journal:  Mol Pain       Date:  2008-04-21       Impact factor: 3.395

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Review 4.  How can sensitive dentine become hypersensitive and can it be reversed?

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6.  Left-shifted nav channels in injured bilayer: primary targets for neuroprotective nav antagonists?

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8.  The MMP-9/TIMP-1 axis controls the status of differentiation and function of myelin-forming Schwann cells in nerve regeneration.

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9.  Unmyelinated nerve fibers in the human dental pulp express markers for myelinated fibers and show sodium channel accumulations.

Authors:  Michael A Henry; Songjiang Luo; S Rock Levinson
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10.  The alternatively spliced fibronectin CS1 isoform regulates IL-17A levels and mechanical allodynia after peripheral nerve injury.

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