The sympathetic nervous system contributes to certain types of chronic pain states such as complex regional pain syndrome (CRPS). Many studies have evaluated sympathetic modulation of nociceptors utilizing animal models of hyperalgesia that typically involve a peripheral nerve injury. These studies have demonstrated that NPY, a sympathetically derived neuropeptide, provides an important although highly complex neuromodulatory function after peripheral nerve injury. However, few studies have evaluated NPY modulation of nociceptors under control or """"""""in-injured"""""""" conditions, which is the broad objective of this research proposal. We believe that understanding how NPY functions under basal conditions is critical to understanding how it functions in response to injury.
The specific aims are: 1) to characterize the pharmacological effects of NPY receptor agonists for modulating the initiation of neurogenic inflammation; 2) to determine whether NPY receptor agonists inhibit capsaicin-evoked hyperalgesia following administration to the rat dental pulp; 3) to evaluate the molecular basis for NPY pharmacology by identifying specific NPY receptor subtypes expressed on the capsaicin-sensitive class of trigeminal sensory neurons and 4) to evaluate the effects of nerve injury on specific aims #1-3. Collectively, these parametric, integrated and multidisciplinary research plan will seen to both address an important scientific question, and to provide an excellent opportunity for comprehensive scientific training.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30DE014326-04
Application #
6774773
Study Section
NIDCR Special Grants Review Committee (DSR)
Program Officer
Hardwick, Kevin S
Project Start
2002-08-01
Project End
2005-07-31
Budget Start
2004-08-01
Budget End
2005-07-31
Support Year
4
Fiscal Year
2004
Total Cost
$33,911
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Dentistry
Type
Schools of Dentistry
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Gibbs, J L; Hargreaves, K M (2008) Neuropeptide Y Y1 receptor effects on pulpal nociceptors. J Dent Res 87:948-52
Gibbs, J L; Diogenes, A; Hargreaves, K M (2007) Neuropeptide Y modulates effects of bradykinin and prostaglandin E2 on trigeminal nociceptors via activation of the Y1 and Y2 receptors. Br J Pharmacol 150:72-9
Gibbs, Jennifer L; Flores, Christopher M; Hargreaves, Kenneth M (2006) Attenuation of capsaicin-evoked mechanical allodynia by peripheral neuropeptide Y Y1 receptors. Pain 124:167-74
Gibbs, J; Flores, C M; Hargreaves, K M (2004) Neuropeptide Y inhibits capsaicin-sensitive nociceptors via a Y1-receptor-mediated mechanism. Neuroscience 125:703-9
Unterbrink, A; O'Sullivan, M; Chen, S et al. (2002) TGF beta-1 downregulates DMP-1 and DSPP in odontoblasts. Connect Tissue Res 43:354-8