Voltage-gated sodium channels are critical to the initiation and propagation of nerve action potentials and some sodium channel (NaCh) isoforms are preferentially expressed in primary afferent nociceptors. Experimental animal and a few human studies have shown changes in the distribution and expression of certain isoforms within primary afferent neurons associated with peripheral inflammation and following nerve injury. These alterations implicate dynamic NaCh expression as a basic underlying mechanism contributing to inflammatory and neuropathic pain. The tooth pulp is a rich source of pain fibers and represents a valuable model system to study pain mechanisms. Normal wisdom teeth and diseased teeth with a diagnosis of irreversible pulpitis and known pain levels are commonly extracted, providing an ample supply of tissues for analysis. The responses to sensory stimuli can be evaluated prior to extraction, thus allowing a possible correlation of NaCh expression with receptor expression for various stimuli. The overall objective of this study is to correlate changes in NaCh expression with changes in hot and cold thermoreceptors to pain levels and clinical responses to hot and cold stimuli in normal and diseased human extracted teeth. NaCh and thermoreceptor expressions will be quantified in normal and in modaUty-specific pain groups of diseased teeth. We hypothesize that in painful teeth the expression of NaCh isoforms dynamically changes, and further that these changes will correlate temporally and spatially with the expression of appropriate thermoreceptors in hot or cold sensitive painful teeth when compared to normal teeth. In a more general sense, the extracted tooth represents a powerful model system to evaluate in a quantitative fashion a possible correlation between known pain states and the alterations in diseased human tissues at the molecular level. Findings from this study will further our knowledge regarding both basic pain mechanisms and the increased occurrence of local anesthesia failures in diseased teeth that can be a major deterrent for utilization of dental care.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE015576-01A1
Application #
6871687
Study Section
Somatosensory and Chemosensory Systems Study Section (SCS)
Program Officer
Kusiak, John W
Project Start
2005-01-01
Project End
2005-08-31
Budget Start
2005-01-01
Budget End
2005-08-31
Support Year
1
Fiscal Year
2005
Total Cost
$122,306
Indirect Cost
Name
University of Colorado Denver
Department
Dentistry
Type
Schools of Dentistry
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Loyd, Dayna R; Henry, Michael A; Hargreaves, Kenneth M (2013) Serotonergic neuromodulation of peripheral nociceptors. Semin Cell Dev Biol 24:51-7
Brandao, Katherine E; Dell'Acqua, Mark L; Levinson, S Rock (2012) A-kinase anchoring protein 150 expression in a specific subset of TRPV1- and CaV 1.2-positive nociceptive rat dorsal root ganglion neurons. J Comp Neurol 520:81-99
Levinson, Simon R; Luo, Songjiang; Henry, Michael A (2012) The role of sodium channels in chronic pain. Muscle Nerve 46:155-65
Henry, Michael A; Luo, Songjiang; Levinson, S Rock (2012) Unmyelinated nerve fibers in the human dental pulp express markers for myelinated fibers and show sodium channel accumulations. BMC Neurosci 13:29
Jeske, Nathaniel A; Por, Elaine D; Belugin, Sergei et al. (2011) A-kinase anchoring protein 150 mediates transient receptor potential family V type 1 sensitivity to phosphatidylinositol-4,5-bisphosphate. J Neurosci 31:8681-8
Loyd, Dayna R; Weiss, Gabriela; Henry, Michael A et al. (2011) Serotonin increases the functional activity of capsaicin-sensitive rat trigeminal nociceptors via peripheral serotonin receptors. Pain 152:2267-76
Ferraz, Caio Cezar Randi; Henry, Michael A; Hargreaves, Kenneth M et al. (2011) Lipopolysaccharide from Porphyromonas gingivalis sensitizes capsaicin-sensitive nociceptors. J Endod 37:45-8
Luo, S; Perry, G M; Levinson, S R et al. (2010) Pulpitis increases the proportion of atypical nodes of Ranvier in human dental pulp axons without a change in Nav1.6 sodium channel expression. Neuroscience 169:1881-7
Fehrenbacher, Jill C; Sun, Xiaoling X; Locke, Erin E et al. (2009) Capsaicin-evoked iCGRP release from human dental pulp: a model system for the study of peripheral neuropeptide secretion in normal healthy tissue. Pain 144:253-61
Henry, Michael A; Luo, Songjiang; Foley, Benjamin D et al. (2009) Sodium channel expression and localization at demyelinated sites in painful human dental pulp. J Pain 10:750-8

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