We explored that MB treatment can lessen the severity EAE and hypothesized the mechanisms underlying its effects.
MB treatment inhibited the development and progression of EAE and mitigated inflammation by reducing inflammatory infiltrates, demyelination and axonal loss.
MB treatment inhibited inflammatory responses by activating the AMPK/SIRT1 pathway and suppressing the activation of NF-κB.
MB treatment could modulate the Th17/Treg immune response to alleviate EAE.