Nadeem Khan1, Sriram P. Mupparaju1, Dionyssios Mintzopoulos2,3, Meenu Kesarwani2,4, Valeria Righi2,3, Laurence G. Rahme2,5, Harold M. Swartz1, A Aria Tzika2,3
1EPR Center for Viable Systems,
Department of Diagnostic Radiology, Dartmouth Medical School, Hanover, NH, USA;
2NMR Surgical Laboratory, MGH & Shriners Hospitals, Harvard
Medical School, Boston, MA, USA; 3Radiology, Athinoula A. Martinos
Center for Biomedical Imaging, Boston, MA, USA; 4Molecular Surgical
Laboratory, MGH & Shriners Hospitals, Harvard Medical School, Boston, MA; 5Molecular
Surgical Laboratory, MGH & Shriners Hospitals, Harvard Medical School,
Boston, MA, USA
Using in vivo electron paramagnetic resonance (EPR) on a 1.2 GHz (L-band) EPR spectrometer, we longitudinally evaluated oxidative stress in a burn trauma model to the left hind limb of mice. The EPR measurements confirm genomic results, which indicated down-regulation of antioxidant genes and strongly suggest dysfunction of the mitochondrial oxidative system. Thus, EPR, which allows the direct measurement of tissue parameters such as pO2, redox status, and reactive oxygen species (ROS), may be used to complement nuclear magnetic resonance (NMR), to better assess tissue damage and the therapeutic effectiveness of antioxidant agents in burn trauma.