An emerging concept in mechanisms that lead to neuropathic pain is elevated intracellular levels of reactive oxygen species (ROS) in peripheral and central sensitization. The overall hypothesis of the PPG is that ROS act as key signaling molecules in concert with other signaling pathways involved in sensitization. In that context, the present proposal examines spinal cord injury (SCI) induced chronic central neuropathic pain (CNP). This is a major public health problem;consequently, an understanding of the mechanisms of CNP will lead to opportunities for treatment of this terrible condition. We will use the rodent spinal cord contusion model because this model best approximates human SCI. CNP in this model includes above level (C7/C8, forelimb innervation), at level (T8, trunk innervation) and below level (L4/L5, hindlimb innervation) pain-like behaviors seen clinically. CNP is thought to be generated in these different clinically relevant regions by different mechanisms. In this project, we will test the hypothesis that generation of ROS after SCI contributes to central neuropathic pain by both peripheral and central sensitization via activated calcium/calmodulin kinase II (pCamKII) pathways. We will test the following specific aims: 1) Determine the time course of development of CNP behavior in the rodent contusion model. 2) Determine the time course of development of central and peripheral sensitization above level, at level and below level after SCI. 3) Test the sites of action of ROS inhibitors and the effects of these substances separately at those sites on CNP behaviors early and in chronic SC and on pCamKII expression levels. 4) Determine the effect of ROS inhibition (by the most effective agent and route determined by behavioral outcomes in Specific Aim 3) on central and peripheral sensitization early and in chronic SCI and on ROS expression levels. Outcome measures include behavior, electrophysiology, protein expression and immunocytochemistry. Our results will expand on Project 1 (ROS in peripheral sensitization after inflammation), Project 3 (role of ROS in C-fiber driven central sensitization) and Project 4 (role of ROS in amygdala and central sensitization) to give insight into mechanisms that provide common bases for development and maintenance of CNP and indicate therapeutically useful strategies for intervention in neuropathic and inflammatory pain syndromes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS011255-36
Application #
8375569
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Project Start
Project End
Budget Start
2012-04-01
Budget End
2013-03-31
Support Year
36
Fiscal Year
2012
Total Cost
$408,156
Indirect Cost
$231,554
Name
University of Texas Medical Br Galveston
Department
Type
DUNS #
800771149
City
Galveston
State
TX
Country
United States
Zip Code
77555
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