TY - JOUR
T1 - Raman spectroscopic investigation of spinal cord injury in a rat model
AU - Saxena, Tarun
AU - Deng, Bin
AU - Stelzner, Dennis
AU - Hasenwinkel, Julie
AU - Chaiken, Joseph
N1 - Funding Information:
A fellowship from the Syracuse Biomaterials Institute supported Tarun Saxena. Kyle Hoellger and Karan Shertukde assisted in the collection of data from healthy and contused spinal cords. Machine shop fabrication was by Lou Buda, Charlie Brown, Phil Arnold and Les Schmutzler. Sally Prasch at the glass shop fabricated the cuvettes. Assistance with the design and optimization of our optical system that was provided by LighTouch Medical and by Rebecca J. Bussjager and discussions regarding the neurology in general with Dr. George Shaheen are gratefully acknowledged. Assistance in the implementation of the KNN algorithm by Arun Subramanian is greatly appreciated. Critical reading of the manuscript by Dr. Jeremy Gilbert is greatly appreciated. Assistance in immunohistological preparations by Karen Hughes and Grazyna Rygiel is greatly appreciated. Funding of the Syracuse University REU program made the participation of Kyle Hoellger possible.
PY - 2011/2
Y1 - 2011/2
N2 - Raman spectroscopy was used to study temporal molecular changes associated with spinal cord injury (SCI) in a rat model. Raman spectra of saline-perfused, injured, and healthy rat spinal cords were obtained and compared. Two injury models, a lateral hemisection and a moderate contusion were investigated. The net fluorescence and the Raman spectra showed clear differences between the injured and healthy spinal cords. Based on extensive histological and biochemical characterization of SCI available in the literature, these differences were hypothesized to be due to cell death, demyelination, and changes in the extracellular matrix composition, such as increased expression of proteoglycans and hyaluronic acid, at the site of injury where the glial scar forms. Further, analysis of difference spectra indicated the presence of carbonyl containing compounds, hypothesized to be products of lipid peroxidation and acid catalyzed hydrolysis of glycosaminoglycan moieties. These results compared well with in vitro experiments conducted on chondroitin sulfate sugars. Since the glial scar is thought to be a potent biochemical barrier to nerve regeneration, this observation suggests the possibility of using near infrared Raman spectroscopy to study injury progression and explore potential treatments ex vivo, and ultimately monitor potential remedial treatments within the spinal cord in vivo.
AB - Raman spectroscopy was used to study temporal molecular changes associated with spinal cord injury (SCI) in a rat model. Raman spectra of saline-perfused, injured, and healthy rat spinal cords were obtained and compared. Two injury models, a lateral hemisection and a moderate contusion were investigated. The net fluorescence and the Raman spectra showed clear differences between the injured and healthy spinal cords. Based on extensive histological and biochemical characterization of SCI available in the literature, these differences were hypothesized to be due to cell death, demyelination, and changes in the extracellular matrix composition, such as increased expression of proteoglycans and hyaluronic acid, at the site of injury where the glial scar forms. Further, analysis of difference spectra indicated the presence of carbonyl containing compounds, hypothesized to be products of lipid peroxidation and acid catalyzed hydrolysis of glycosaminoglycan moieties. These results compared well with in vitro experiments conducted on chondroitin sulfate sugars. Since the glial scar is thought to be a potent biochemical barrier to nerve regeneration, this observation suggests the possibility of using near infrared Raman spectroscopy to study injury progression and explore potential treatments ex vivo, and ultimately monitor potential remedial treatments within the spinal cord in vivo.
KW - Chondroitin sulfate proteoglycans
KW - Glial scar
KW - Raman spectroscopy
KW - Spinal cord injury
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U2 - 10.1117/1.3549700
DO - 10.1117/1.3549700
M3 - Article
C2 - 21361706
AN - SCOPUS:79957817869
SN - 1083-3668
VL - 16
JO - Journal of biomedical optics
JF - Journal of biomedical optics
IS - 2
M1 - 027003
ER -