The goal of this project is to demonstrate the ability of the nitroxide antioxidant, tempol to oppose irreversible loss of locomotor function due to spinal cord injury (SCI). Presently, only methylprednisolone has been shown to have efficacy in humans for SCI. However, the extent of recovery is limited. Potentially superior countermeasures are available, but require a demonstration of efficacy in an appropriate animal model of SCI before use in patient trials. The proposed studies are based on our preliminary data, in which tempol, which is neuroprotective increased locomotor function following SCI. We will determine the efficacy of treatment with tempol alone and in combination with methylpednisolone or improving locomotor function and sparing spinal cord tissue following chronic injury in an established model of SCI developed by the Multicenter Animal Spinal Cord Injury Study (MASCIS). Optimization of tempol treatment may lead to a therapeutic modality for SCI.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43NS047760-01A1
Application #
6834355
Study Section
Special Emphasis Panel (ZRG1-BDCN-E (11))
Program Officer
Kleitman, Naomi
Project Start
2004-07-01
Project End
2005-06-30
Budget Start
2004-07-01
Budget End
2005-06-30
Support Year
1
Fiscal Year
2004
Total Cost
$100,000
Indirect Cost
Name
Motogen, Inc.
Department
Type
DUNS #
052615395
City
Mount Kisco
State
NY
Country
United States
Zip Code
10549
Zeman, Richard J; Wen, Xialing; Ouyang, Nengtai et al. (2008) Stereotactic radiosurgery improves locomotor recovery after spinal cord injury in rats. Neurosurgery 63:981-7;discussion 987-8
Hillard, Virany H; Peng, Hong; Das, Kaushik et al. (2007) Inhibition of x-irradiation-enhanced locomotor recovery after spinal cord injury by hyperbaric oxygen or the antioxidant nitroxide tempol. J Neurosurg Spine 6:337-43
Zeman, Richard J; Peng, Hong; Feng, Yong et al. (2006) Beta2-adrenoreceptor agonist-enhanced recovery of locomotor function after spinal cord injury is glutathione dependent. J Neurotrauma 23:170-80