The application is for renewal of a grant that has supported a long-term investigation of mechanisms of nociception and antinociception. The eventual goal of the proposed studies is to learn how plastic changes in nociceptive responses lead to persistent pain and to develop new approaches for chronic pain therapy. The overall hypothesis of the present proposal is that nociceptive transmission in the spinal cord is regulated by protein kinases and phosphatases through phosphorylation and dephosphorylaion of synaptic receptors and of proteins involved in intracellular signal transduction pathways. The outcome of this regulation can be central sensitization (or conversely, long-lasting inhibition) of nociceptive neurons, such as spinothalamic tract (STT) cells, as well as changes in gene expression in nociceptive neurons. Central sensitization, which has been suggested to underlie secondary allodynia and hyperalgesia, is proposed to depend at least in part on postsynaptic changes in STT cells.
Specific Aim 1 is to determine if different protein kinases are activated in STT cells and if different protein kinases contribute to differences in the responses of STT cells to innocuous and noxious stimuli, leading to different balances of allodynia and hyperalgesia.
Specific Aim 2 is to determine if the induction of central sensitization, like long-term potentiation, depends on the activation of calmodulin and calcium/calmodulin-dependent kinase II (CaMKII).
Specific Aim 3 is to determine if phosphorylation of amino acid receptors occurs in STT cells during central sensitization and to investigate how inhibition of CaMKII permits the expression of along-lasting inhibition.
Specific Aim 4 is to determine if agents that alter central sensitization also alter the expression of inducible immediate, early genes and phosphorylation of constitutive transcription factors. The experimental approaches that will be used include the analysis of behavioral changes, electrophysiological recordings and pharmacological modulation of proteins involved in nociceptive signal transduction, and immunohistochemical and Western blotting studies, using antibodies to non-phosphorylated and phosphorylated proteins that contribute to the structure of glutamate receptors or belong to signal transduction pathways.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS009743-35
Application #
6792056
Study Section
Special Emphasis Panel (ZRG1-IFCN-5 (03))
Program Officer
Porter, Linda L
Project Start
1975-05-01
Project End
2005-07-31
Budget Start
2004-08-01
Budget End
2005-07-31
Support Year
35
Fiscal Year
2004
Total Cost
$372,500
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Neurosciences
Type
Schools of Medicine
DUNS #
800771149
City
Galveston
State
TX
Country
United States
Zip Code
77555
Willis Jr, William D (2009) The role of TRPV1 receptors in pain evoked by noxious thermal and chemical stimuli. Exp Brain Res 196:5-11
Sun, R; Yan, J; Willis, W D (2007) Activation of protein kinase B/Akt in the periphery contributes to pain behavior induced by capsaicin in rats. Neuroscience 144:286-94
Saab, C Y; Willis, W D (2002) Cerebellar stimulation modulates the intensity of a visceral nociceptive reflex in the rat. Exp Brain Res 146:117-21
Saab, C Y; Willis, W D (2001) Nociceptive visceral stimulation modulates the activity of cerebellar Purkinje cells. Exp Brain Res 140:122-6
Willis Jr, W D (1999) Dorsal root potentials and dorsal root reflexes: a double-edged sword. Exp Brain Res 124:395-421
Wu, J; Lin, Q; Lu, Y et al. (1998) Changes in nitric oxide synthase isoforms in the spinal cord of rat following induction of chronic arthritis. Exp Brain Res 118:457-65
Tsuruoka, M; Willis, W D (1998) Involvement of the locus coeruleus in analgesic effects of a low dose of naloxone during the inflammatory process. Exp Brain Res 119:166-70
Peng, Y B; Lin, Q; Willis, W D (1997) Involvement of protein kinase C in responses of rat dorsal horn neurons to mechanical stimuli and periaqueductal gray descending inhibition. Exp Brain Res 114:561-70
Lin, Q; Peng, Y; Willis, W D (1994) Glycine and GABAA antagonists reduce the inhibition of primate spinothalamic tract neurons produced by stimulation in periaqueductal gray. Brain Res 654:286-302
Rees, H; Sluka, K A; Westlund, K N et al. (1994) Do dorsal root reflexes augment peripheral inflammation? Neuroreport 5:821-4

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