Angiogenesis occurs in response to traumatic spinal cord injury (SCI). However, the role of angiogenesis in SCI is controversial. Based on our preliminary in vivo longitudinal magnetic resonance imaging (MRI), neurobehavioral, and end point histology studies, we hypothesize that angiogenesis is beneficial to recovery from SCI. We propose to verify this hypothesis by modulating the angiogenic activity by acute and long term administration of vascular endothelial growth factor (VEGF; for promoting angiogenesis) and anti-VEGF (neutralizing the effects of endogenous VEGF) in experimental SCI. The effect of these compounds will be assessed by combining in vivo longitudinal multi-modal magnetic resonance imaging (MRI) with immunohistochemical studies and neurobehavioral studies. The multi-modal MRI studies include high resolution anatomical, diffusion tensor imaging (DTI), magnetization transfer imaging (MTI), perfusion imaging, and dynamic contrast enhanced MRI (DCE MRI). DTI and MTI will be used to probe the integrity of fiber tracts while DCE MRI and perfusion MRI will allow us to identify and characterize the neovasculature, determine the vascular density, and map the blood-spinal cord permeability. Sophisticated image processing techniques will be implemented for generating and displaying the neovasculature. The temporal changes in the endogenous VEGF expression and its correlation with angiogenic activity following SCI will be investigated for interpreting the MRI results on a rational basis. Detailed immunohistochemical studies will be performed for identifying neovasculature. The MRI measures will be correlated with neurobehavioral scores If the role of angiogenesis in recovery from SCI is confirmed, it should be possible to treat SCI subjects with drugs that manipulate the angiogenic activity to augment the endogenous repair processes. In addition, it is possible to modulate angiogenesis in conjunction with other treatments, such as cellular grafts to further enhance the recovery from SCI. Thus the proposed studies have a very high degree of clinical relevance. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS045624-03
Application #
7263071
Study Section
Clinical Neuroplasticity and Neurotransmitters Study Section (CNNT)
Program Officer
Kleitman, Naomi
Project Start
2005-08-03
Project End
2010-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
3
Fiscal Year
2007
Total Cost
$568,068
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77225
Qian, Junchao; Herrera, Juan J; Narayana, Ponnada A (2010) Neuronal and axonal degeneration in experimental spinal cord injury: in vivo proton magnetic resonance spectroscopy and histology. J Neurotrauma 27:599-610
Herrera, Juan J; Sundberg, Laura M; Zentilin, Lorena et al. (2010) Sustained expression of vascular endothelial growth factor and angiopoietin-1 improves blood-spinal cord barrier integrity and functional recovery after spinal cord injury. J Neurotrauma 27:2067-76
Sundberg, Laura M; Herrera, Juan J; Narayana, Ponnada A (2010) In vivo longitudinal MRI and behavioral studies in experimental spinal cord injury. J Neurotrauma 27:1753-67
Esparza-Coss, Emilio; Wosik, Jarek; Narayana, Ponnada A (2010) Perfusion in rat brain at 7 T with arterial spin labeling using FAIR-TrueFISP and QUIPSS. Magn Reson Imaging 28:607-12
Nesic, Olivera; Sundberg, Laura M; Herrera, Juan J et al. (2010) Vascular endothelial growth factor and spinal cord injury pain. J Neurotrauma 27:1793-803
Patel, Chirag B; Cohen, David M; Ahobila-Vajjula, Pallavi et al. (2009) Effect of VEGF treatment on the blood-spinal cord barrier permeability in experimental spinal cord injury: dynamic contrast-enhanced magnetic resonance imaging. J Neurotrauma 26:1005-16
Mogatadakala, Kishore V; Narayana, Ponnada A (2009) In vivo diffusion tensor imaging of thoracic and cervical rat spinal cord at 7 T. Magn Reson Imaging 27:1236-41
Herrera, Juan J; Nesic, Olivera; Narayana, Ponnada A (2009) Reduced vascular endothelial growth factor expression in contusive spinal cord injury. J Neurotrauma 26:995-1003
Cohen, David M; Patel, Chirag B; Ahobila-Vajjula, Pallavi et al. (2009) Blood-spinal cord barrier permeability in experimental spinal cord injury: dynamic contrast-enhanced MRI. NMR Biomed 22:332-41
Mogatadakala, Kishore V; Bankson, James A; Narayana, Ponnada A (2008) Three-element phased-array coil for imaging of rat spinal cord at 7T. Magn Reson Med 60:1498-505

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