Spinal cord injury (SCI) is a major health and socio-economic problem, affecting many individuals. Magnetic resonance imaging (MRI) provides in vivo three-dimensional images with exquisite soft tissue contrast for investigating injured spinal cord (SC). In experimental studies with rat models of SCI, we regularly use MRI to follow the same animal longitudinally, so that each animal can serve as its own control. Conventional MRI, however, provides limited information on vascular changes that occur transiently following the injury. Novel imaging methods with capacity to sense vascular changes are required. As potential imaging approaches, we have recently explored MR angiography (MRA) and perfusion MRI (P- MRI) techniques for probing the vascular system of rat SC. Our preliminary data showed that MRA is capable of producing high-resolution maps of macrovascular projections that supply blood to the rat SC while P-MRI is sensitive to the microvasculature within the cord tissue. Using the contrast agent gadopentate dimeglumine (Gd), we also generated angiograms that delineate the spinal vessels in greater detail. In longitudinal dynamic contrast-enhanced MRI (DCE-MRI) studies, we have previously quantified the temporal changes in permeability of blood-spinal cord barrier (BSCB) following the injury and detected the neovasculature in injured cord. Based on these preliminary results, we hypothesize that the combination of the imaging modalities (anatomical MRI, MRA, P-MRI and DCE-MRI) will increase the reliability, sensitivity and specificity of detecting morphological and vascular changes in injured SC. The MR-based measurements will provide valuable direct information on pathology, physiology and function of injured SC non-invasively, and may serve as a predictor of the final neurologic outcome from SCI. To test this hypothesis, we will perform high resolution in vivo imaging using implantable radio frequency coil in longitudinal studies of SC on injured and control rats. In conjunction with imaging, we will also carry out standard neurobehavioral tests on the animals recovering from the injury and perform quantitative end-point histological analysis on the injured cord tissue. We will statistically compare the MR-based measurements with the behavioral scores and histological findings to determine the endogenous vascular plasticity in injured SC and its role in recovery from SCI. A non-invasive determination of reorganization in vascular network of SC that is associated with the recovery of function following SCI will be a large step forward in understanding the recovery mechanisms, and in long term, objective assessment of potential new therapies with power to manipulate the SC vasculature with or without the use of exogenous processes to improve the neurofunctional outcome. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS054019-02
Application #
7244038
Study Section
Clinical Neuroplasticity and Neurotransmitters Study Section (CNNT)
Program Officer
Kleitman, Naomi
Project Start
2006-07-01
Project End
2007-10-31
Budget Start
2007-07-01
Budget End
2007-10-31
Support Year
2
Fiscal Year
2007
Total Cost
$23,150
Indirect Cost
Name
University of Kansas
Department
Physiology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Chou, Peter Cheng-te; Shunmugavel, Anandakumar; El Sayed, Hanaa et al. (2011) Preclinical use of longitudinal MRI for screening the efficacy of S-nitrosoglutathione in treating spinal cord injury. J Magn Reson Imaging 33:1301-11
Tatar, Ilkan; Chou, Peter Cheng-te; Desouki, Mohamed Mokhtar et al. (2009) Evaluating regional blood spinal cord barrier dysfunction following spinal cord injury using longitudinal dynamic contrast-enhanced MRI. BMC Med Imaging 9:10
Huang, Min; Huang, Zhixin L; Bilgen, Mehmet et al. (2008) Magnetic resonance imaging of contrast-enhanced polyelectrolyte complexes. Nanomedicine 4:30-40