This study aimed to determine the extent of axon diameter distribution changes in the lumbar spinal cord in C57BL/6 mice associated with experimental autoimmune encephalomyelitis (EAE). AxCaliber protocol was performed ex-vivo at 16.4T to analyze changes in mice with a range of EAE severity and the effect of treatment with alpha-lipoic acid (R-ALA), a nutraceutical compound that is recently known for suppressing microglial activation and CNS inflammation in EAE rodent models. AxCaliber showed axon diameter increases in mild relapsing remitting EAE group after R-ALA treatment. This might indicate a process of remyelination or other microstructural changes.
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