RSNA 2009 

Abstract Archives of the RSNA, 2009


LL-NM2014-B04

Evaluation of Neuroinflammation in Experimental Autoimmune Encephalomyelitis Mice with Micro Positron Emission Tomography and Micro Magnetic Resonance Imaging

Scientific Posters

Presented on November 29, 2009
Presented as part of LL-NM-B: Nuclear Medicine

Participants

Hong Liu MD, PhD, Presenter: Nothing to Disclose
Michael S. Valerio BS, Abstract Co-Author: Nothing to Disclose
Jungmin Han, Abstract Co-Author: Nothing to Disclose
Rutao Yao PHD, , Abstract Co-Author: Nothing to Disclose
Hani H. Abdel-Nabi MD, PhD, Abstract Co-Author: Nothing to Disclose
Murali Ramanathan PhD, Abstract Co-Author: Nothing to Disclose
Bianca Weinstock-Guttman MD, Abstract Co-Author: Nothing to Disclose
Atif Awad PhD, Abstract Co-Author: Nothing to Disclose

PURPOSE

Experimental autoimmune encephalomyelitis (EAE) is a widely utilized animal model of multiple sclerosis. There is still no solid method to detect the real-time immune process in vivo. This study will investigate whether [18F] Fluoro-2-deoxy-D-glucose (FDG) micro Positron Emission Tomography (PET) in conjunction with Magnetic Resonance Imaging (MRI) could be used to monitor EAE development and this approach is sensitive enough to evaluate phytosterol (plant sterol) therapeutic effect. Phytosterol has been proved to modulate immune response in vitro.

METHOD AND MATERIALS

EAE was induced in 10 weeks old female SJL mice by administration of proteolipid protein (PLP139-151) peptide and pertusis. There were two groups of mice, 6 mice in each group. Phytosterol or placebo oral route treatment started 7 days before EAE induction. The treatment continued until sacrificed after onset of EAE. Mice were scanned by microPET and microMRI at two time-points: before induction EAE and onset of EAE. 18F-FDG was administered through IP injection.

RESULTS

Significant increased FDG uptake was observed in spinal cord of EAE mice compared with that of normal controls. There was no obvious central nervous system lesion under microMRI study during the onset of EAE.

CONCLUSION

PET is more sensitive than MRI to detect the early neuroinflammation process during the onset of EAE. Serial 18F-FDG PET imaging could be applied to monitor autoimmune disease development in vivo and potentially evaluate the therapeutic effects. In addition, IP administration of FDG is a reliable and convenient method.

CLINICAL RELEVANCE/APPLICATION

The current study will expand the clinical application of PET in the field of neuroimaging.

Cite This Abstract

Liu, H, Valerio, M, Han, J, Yao, R, Abdel-Nabi, H, Ramanathan, M, Weinstock-Guttman, B, Awad, A, Evaluation of Neuroinflammation in Experimental Autoimmune Encephalomyelitis Mice with Micro Positron Emission Tomography and Micro Magnetic Resonance Imaging.  Radiological Society of North America 2009 Scientific Assembly and Annual Meeting, November 29 - December 4, 2009 ,Chicago IL. http://archive.rsna.org/2009/8004773.html